GlyCosmos Portal

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GlyCosmos Genes

Integrated list of glycan-related genes extracted KEGG GENES Database, UniProt, GlycoGene Database (GGDB), Plant GARDEN and FlyGlycoDB. Glycan-related genes including glycosyltransferase, hydrolase activity (acting on glycosyl bonds), carbohydrate metabolic process, etc .

Source	Last Updated
FlyGlycoDB	March 25, 2024
GlycoGene Database (GGDB)	January 26, 2018
KEGG GENES Database	September 20, 2023
Plant GARDEN	May 28, 2020
UniProt	July 8, 2024

Selecting the function you want to look up from the categories displays a list narrowed down to glycan-related genes with that function (Gene Ontology).

Catalytic activity

glycosyltransferase activity

hydrolase activity, acting on glycosyl bonds

Binding

carbohydrate binding

Response to carbohydrate

Primary metabolic process

Displaying entries **826 - 850** of **1582** in total

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Gene ID	Gene Name	Gene Symbol ▲	Organism	Disease Ontology
152831	klotho beta	KLB Aliases: b-Klotho	Homo sapiens (human)	Clostridium difficile colitis allergic rhinitis autosomal dominant hypophosphatemic rickets breast cancer breast carcinoma cancer cartilage-hair hypoplasia diabetes mellitus diabetic ketoacidosis diarrhea disease of metabolism embryoma familial hyperlipidemia gestational diabetes hepatocellular carcinoma intrahepatic cholestasis of pregnancy invasive ductal carcinoma irritable bowel syndrome kidney disease kidney failure liver cancer lung cancer lung non-small cell carcinoma neurocirculatory asthenia nodular prostate obesity ovarian disease papillary adenocarcinoma papillary renal cell carcinoma prostate cancer prostate carcinoma prostatic adenoma steatotic liver disease thyroid adenoma thyroid cancer thyroid gland anaplastic carcinoma thyroid gland carcinoma thyroid gland follicular carcinoma thyroid gland papillary carcinoma type 2 diabetes mellitus uremia vasomotor rhinitis
3820	killer cell lectin like receptor B1	KLRB1 Aliases: CD161 CLEC5B NKR-P1 NKR-P1A hNKR-P1A natural killer cell surface protein P1A	Homo sapiens (human)	Goodpasture syndrome Takayasu's arteritis acquired immunodeficiency syndrome acute promyelocytic leukemia aggressive NK-cell leukemia allergic asthma arthritis arthropathy asthma autoimmune disease autoimmune lymphoproliferative syndrome type 2A autoimmune lymphoproliferative syndrome type 2B autoimmune lymphoproliferative syndrome type 3 autoimmune lymphoproliferative syndrome bone disease bronchus cancer bronchus carcinoma cancer cartilage disease cataract connective tissue disease eclampsia embryoma familial multiple nevi flammei granulomatosis with polyangiitis hepatitis A hepatitis B hepatitis C hepatitis hepatocellular carcinoma hidradenitis suppurativa hidradenitis human immunodeficiency virus infectious disease immune system disease influenza intermittent claudication intrinsic asthma liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoproliferative syndrome 1 lymphoproliferative syndrome 2 melanoma mitral valve stenosis multiple myeloma multiple sclerosis myocarditis osteoarthritis peeling skin syndrome periodontitis placental insufficiency pneumonia polyarteritis nodosa pompholyx prostate cancer prostate carcinoma psoriatic arthritis rheumatoid arthritis scleroderma skin melanoma spondyloarthropathy spondylosis systemic Epstein-Barr virus positive T-cell lymphoma of childhood systemic lupus erythematosus systemic scleroderma tuberculosis urinary bladder cancer viral infectious disease
3821	killer cell lectin like receptor C1	KLRC1 Aliases: CD159a NKG2-1/B activating NK receptor NKG2-A NKG2-B	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Barrett's esophagus Behcet's disease Graves' disease Japanese encephalitis Kawasaki disease Marfan syndrome Pick's disease Reye syndrome acquired immunodeficiency syndrome adult lymphoma allergic rhinitis autoimmune disease autoimmune hepatitis autoimmune lymphoproliferative syndrome bacterial sepsis cancer central nervous system lymphoma cerebral degeneration childhood lymphoma choriocarcinoma chromophobe renal cell carcinoma chronic myeloid leukemia clear cell renal cell carcinoma collecting duct carcinoma colorectal cancer colorectal carcinoma dengue disease embryoma endometriosis of uterus endometriosis enthesopathy fibromyalgia hematologic cancer hepatitis A hepatitis B hepatitis C hepatitis hepatocellular carcinoma human immunodeficiency virus infectious disease hyperthyroidism immune system disease large intestine cancer leukemia liver cancer liver carcinoma lymphoma melanoma multiple myeloma multiple sclerosis nonpapillary renal cell carcinoma obsolete ymphosarcoma papillary renal cell carcinoma parapsoriasis placenta cancer psoriasis pustulosis of palm and sole renal carcinoma renal cell carcinoma rheumatoid arthritis sarcomatoid renal cell carcinoma situs inversus skin melanoma systemic lupus erythematosus thyrotoxicosis tongue cancer tropical spastic paraparesis tuberous sclerosis vasomotor rhinitis viral infectious disease vitiligo yellow fever
3823	killer cell lectin like receptor C3	KLRC3 Aliases: NKG2-E	Homo sapiens (human)	diabetic ketoacidosis endometrial cancer endometrial carcinoma giant cell glioblastoma glioblastoma obsolete type 1 diabetes mellitus 9 sickle cell anemia type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus uterine corpus cancer
3824	killer cell lectin like receptor D1	KLRD1	Homo sapiens (human)	Behcet's disease Evans' syndrome Peutz-Jeghers syndrome acquired immunodeficiency syndrome acute myeloid leukemia acute promyelocytic leukemia adult lymphoma allergic asthma asthma autoimmune disease autoimmune lymphoproliferative syndrome type 2A autoimmune lymphoproliferative syndrome type 2B autoimmune lymphoproliferative syndrome type 3 autoimmune lymphoproliferative syndrome autoimmune thrombocytopenic purpura bacterial infectious disease cancer central nervous system lymphoma cervix uteri carcinoma in situ chikungunya childhood lymphoma chronic NK-cell lymphocytosis common wart dengue hemorrhagic fever diabetic ketoacidosis embryoma enthesopathy fibromyalgia hepatitis B hepatitis C hepatocellular carcinoma human immunodeficiency virus infectious disease idiopathic scoliosis immune system disease infectious mononucleosis influenza intrinsic asthma liver cancer lung cancer lung non-small cell carcinoma lymphoma lymphoproliferative syndrome 1 lymphoproliferative syndrome 2 multiple sclerosis obsolete malignant histiocytosis obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma primary immunodeficiency disease rheumatoid arthritis systemic Epstein-Barr virus positive T-cell lymphoma of childhood systemic lupus erythematosus tropical spastic paraparesis type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus von Hippel-Lindau disease
346689	killer cell lectin like receptor G2	KLRG2 Aliases: C-type lectin domain family 15, member B CLEC15B FLJ44186	Homo sapiens (human)	prostate cancer prostate carcinoma
22914	killer cell lectin like receptor K1	KLRK1 Aliases: CD314 KLR NKG2-D NKG2D	Homo sapiens (human)	B-cell lymphoma Barrett's esophagus Behcet's disease Burkitt lymphoma Crohn's colitis Crohn's disease Ewing sarcoma Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Kaposi's sarcoma Kawasaki disease Langerhans-cell histiocytosis Sezary's disease X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia acute leukemia acute lymphoblastic leukemia acute monocytic leukemia acute myeloid leukemia acute myocardial infarction adenocarcinoma adenoma adult lymphoma alopecia alveolar echinococcosis anogenital venereal wart arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asbestosis ataxia telangiectasia atherosclerosis atypical chronic myeloid leukemia, BCR-ABL1 negative autoimmune disease autoimmune hepatitis autoimmune lymphoproliferative syndrome basal cell carcinoma benign deep fibrous histiocytoma benign mesothelioma bile duct adenocarcinoma bile duct carcinoma bone osteosarcoma breast cancer breast carcinoma bronchiolitis obliterans bronchiolitis bronchus cancer bronchus carcinoma byssinosis cancer carcinoma celiac disease central nervous system cancer cervical adenocarcinoma cervical cancer cervix carcinoma cervix uteri carcinoma in situ childhood acute myeloid leukemia childhood leukemia childhood lymphoma childhood osteosarcoma cholangiocarcinoma chronic fatigue syndrome chronic monocytic leukemia chronic obstructive pulmonary disease colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congestive heart failure coronary artery disease coronary thrombosis cribriform carcinoma cutaneous fibrous histiocytoma diabetes mellitus diabetic ketoacidosis distal arthrogryposis embryoma encephalitis encephalomyelitis endometriosis of uterus endometriosis epithelioid sarcoma esophagus squamous cell carcinoma familial adenomatous polyposis 1 familial adenomatous polyposis familial hyperlipidemia familial retinoblastoma fibrosarcoma gallbladder disease gastrointestinal system cancer giant cell glioblastoma glioblastoma gliosarcoma granular cell carcinoma hepatitis A hepatitis B hepatitis C hepatitis hepatocellular carcinoma high grade glioma histiocytoma hyperglycemia idiopathic interstitial pneumonia idiopathic pulmonary fibrosis immune system disease inflammatory bowel disease 1 inflammatory bowel disease intrahepatic cholangiocarcinoma islet cell tumor large intestine cancer leukemia leukocyte adhesion deficiency 1 leukocyte adhesion deficiency liver cancer liver carcinoma liver disease lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lupus erythematosus lymphoblastic lymphoma lymphoid leukemia lymphoma lymphoproliferative syndrome malignant mesothelioma melanoma mixed glioma monoclonal gammopathy of uncertain significance monocytic leukemia multiple myeloma multiple sclerosis myelitis myeloid leukemia myocardial infarction myocarditis nasopharynx carcinoma neuroblastoma non-Hodgkin lymphoma obsolete ymphosarcoma osteosarcoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancytopenia paroxysmal nocturnal hemoglobinuria primary sclerosing cholangitis prolactinoma prostate cancer prostate carcinoma refractory plasma cell neoplasm reticulohistiocytic granuloma reticulosarcoma retinoblastoma rheumatoid arthritis sarcoma sclerosing cholangitis sclerosing hemangioma sebaceous carcinoma silent myocardial infarction skin melanoma spindle cell sarcoma spondyloarthropathy spondylosis squamous cell carcinoma squamous cell neoplasm stomach cancer stomach carcinoma sweat gland cancer systemic lupus erythematosus temporal arteritis thyroid gland anaplastic carcinoma tongue squamous cell carcinoma trilateral retinoblastoma tropical spastic paraparesis tuberculosis tubular adenocarcinoma type 2 diabetes mellitus ulcerative colitis viral infectious disease
200185	keratinocyte associated protein 2	KRTCAP2 Aliases: KCP2	Homo sapiens (human)
3897	L1 cell adhesion molecule	L1CAM Aliases: CAML1 CD171 NCAM-L1 neural cell adhesion molecule L1	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Charcot-Marie-Tooth disease type 5 Henoch-Schoenlein purpura Hirschsprung's disease Kallmann syndrome Laron syndrome MASA syndrome Mast syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Rett syndrome Reye syndrome SPOAN syndrome Sheehan syndrome Troyer syndrome X-linked dominant hypophosphatemic rickets achondroplasia acne acute chest syndrome adenomatoid tumor adrenal gland cancer adrenoleukodystrophy alternating hemiplegia of childhood anxiety disorder aphasia atrophic gastritis autism spectrum disorder autistic disorder autonomic neuropathy benign ependymoma benign intermediate mesothelioma benign mesothelioma bile duct adenocarcinoma bile duct carcinoma bipolar disorder bone osteosarcoma brain cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma celiac disease cellular ependymoma central nervous system cancer central nervous system disease cerebral degeneration cervical adenocarcinoma cervical cancer cervix carcinoma childhood ependymoma cholangiocarcinoma chromophobe renal cell carcinoma clear cell renal cell carcinoma clubfoot collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma communicating hydrocephalus congenital hypothyroidism congenital nystagmus craniosynostosis depressive disorder diabetes mellitus differentiated thyroid gland carcinoma dissociated nystagmus duodenum cancer embryoma endometrial adenocarcinoma endometrial cancer endometrial carcinoma epilepsy esophagus squamous cell carcinoma familial retinoblastoma fibromyalgia gastrointestinal stromal tumor giant cell glioblastoma glioblastoma gliosarcoma glucose intolerance heart cancer hepatocellular carcinoma hereditary spastic paraplegia 10 hereditary spastic paraplegia 11 hereditary spastic paraplegia 12 hereditary spastic paraplegia 13 hereditary spastic paraplegia 14 hereditary spastic paraplegia 15 hereditary spastic paraplegia 16 hereditary spastic paraplegia 17 hereditary spastic paraplegia 18 hereditary spastic paraplegia 19 hereditary spastic paraplegia 23 hereditary spastic paraplegia 24 hereditary spastic paraplegia 25 hereditary spastic paraplegia 26 hereditary spastic paraplegia 27 hereditary spastic paraplegia 28 hereditary spastic paraplegia 29 hereditary spastic paraplegia 2 hereditary spastic paraplegia 30 hereditary spastic paraplegia 31 hereditary spastic paraplegia 32 hereditary spastic paraplegia 34 hereditary spastic paraplegia 35 hereditary spastic paraplegia 36 hereditary spastic paraplegia 37 hereditary spastic paraplegia 38 hereditary spastic paraplegia 39 hereditary spastic paraplegia 3A hereditary spastic paraplegia 41 hereditary spastic paraplegia 42 hereditary spastic paraplegia 43 hereditary spastic paraplegia 44 hereditary spastic paraplegia 45 hereditary spastic paraplegia 46 hereditary spastic paraplegia 48 hereditary spastic paraplegia 49 hereditary spastic paraplegia 4 hereditary spastic paraplegia 53 hereditary spastic paraplegia 54 hereditary spastic paraplegia 55 hereditary spastic paraplegia 56 hereditary spastic paraplegia 57 hereditary spastic paraplegia 5A hereditary spastic paraplegia 61 hereditary spastic paraplegia 62 hereditary spastic paraplegia 63 hereditary spastic paraplegia 64 hereditary spastic paraplegia 6 hereditary spastic paraplegia 72A hereditary spastic paraplegia 73 hereditary spastic paraplegia 75 hereditary spastic paraplegia 77 hereditary spastic paraplegia 7 hereditary spastic paraplegia 8 hereditary spastic paraplegia 9A hereditary spastic paraplegia 9B hereditary spastic paraplegia high grade glioma holoprosencephaly 1 holoprosencephaly hydrocephalus hypersensitivity vasculitis hypertropia hypogonadotropic hypogonadism 1 with or without anosmia hypogonadotropic hypogonadism 10 with or without anosmia hypogonadotropic hypogonadism 11 with or without anosmia hypogonadotropic hypogonadism 12 with or without anosmia hypogonadotropic hypogonadism 13 with or without anosmia hypogonadotropic hypogonadism 14 with or without anosmia hypogonadotropic hypogonadism 16 with or without anosmia hypogonadotropic hypogonadism 17 with or without anosmia hypogonadotropic hypogonadism 18 with or without anosmia hypogonadotropic hypogonadism 19 with or without anosmia hypogonadotropic hypogonadism 2 with or without anosmia hypogonadotropic hypogonadism 20 with or without anosmia hypogonadotropic hypogonadism 21 with or without anosmia hypogonadotropic hypogonadism 22 with or without anosmia hypogonadotropic hypogonadism 3 with or without anosmia hypogonadotropic hypogonadism 4 with or without anosmia hypogonadotropic hypogonadism 5 with or without anosmia hypogonadotropic hypogonadism 6 with or without anosmia hypogonadotropic hypogonadism 7 with or without anosmia hypogonadotropic hypogonadism 8 with or without anosmia hypogonadotropic hypogonadism 9 with or without anosmia hypogonadotropic hypogonadism hypopituitarism hypothalamic disease hypothyroidism idiopathic interstitial pneumonia idiopathic pulmonary fibrosis inflammatory bowel disease intellectual disability intracranial hypertension intrahepatic cholangiocarcinoma isolated growth hormone deficiency type IA isolated growth hormone deficiency type IB isolated growth hormone deficiency type II isolated growth hormone deficiency type III isolated growth hormone deficiency kidney cancer large intestine cancer learning disability liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung small cell carcinoma major depressive disorder malignant mesothelioma malignant pleural mesothelioma mechanical strabismus melanoma microcephaly microinvasive gastric cancer microphthalmia mixed glioma mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis VI mucopolysaccharidosis myxedema myxopapillary ependymoma nephrogenic diabetes insipidus nervous system disease neuroblastoma neurotic disorder nonpapillary renal cell carcinoma obsolete Matthew-Wood syndrome obsolete intestinal pseudo-obstruction obstructive hydrocephalus ophthalmoplegia osteosarcoma ovarian cancer ovarian carcinoma pancreatic adenocarcinoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma pancreatic ductal carcinoma panhypopituitarism papillary adenocarcinoma papillary ependymoma papillary renal cell carcinoma paralytic ileus paraplegia parathyroid gland disease pathologic nystagmus pheochromocytoma phobic disorder prediabetes syndrome primary biliary cholangitis prostate cancer prostate carcinoma pseudotumor cerebri renal carcinoma renal cell carcinoma restless legs syndrome retinoblastoma rickets sarcomatoid carcinoma sarcomatoid renal cell carcinoma schizophrenia seminoma senile degeneration of brain skin melanoma small intestine cancer spontaneous ocular nystagmus squamous cell carcinoma stomach cancer stomach carcinoma strabismus syndromic X-linked intellectual disability 94 systemic lupus erythematosus tanycytic ependymoma testicular cancer testis seminoma thymus gland disease thyroid adenoma thyroid cancer thyroid gland anaplastic carcinoma thyroid gland carcinoma thyroid gland papillary carcinoma tongue squamous cell carcinoma transitional cell carcinoma trilateral retinoblastoma type 2 diabetes mellitus uterine cancer uterine carcinosarcoma uterine corpus cancer
79944	L-2-hydroxyglutarate dehydrogenase	L2HGDH Aliases: 2-hydroxyglutarate dehydrogenase FLJ12618	Homo sapiens (human)	2-hydroxyglutaric aciduria D-2-hydroxyglutaric aciduria 1 D-2-hydroxyglutaric aciduria L-2-hydroxyglutaric aciduria brain cancer cerebellar ataxia chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma congenital nystagmus disease of metabolism dissociated nystagmus dystonia encephalitis encephalomyelitis epilepsy giant cell glioblastoma glioblastoma hereditary spastic paraplegia high grade glioma hypertropia intellectual disability learning disability mechanical strabismus myelitis nervous system cancer neurodegenerative disease nonpapillary renal cell carcinoma ophthalmoplegia optic atrophy papillary renal cell carcinoma pathologic nystagmus renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma sensorineural hearing loss spontaneous ocular nystagmus strabismus syndromic X-linked intellectual disability 94 vascular dementia visual epilepsy
144811	laccase domain containing 1	LACC1 Aliases: FAMIN FLJ38725 fatty acid metabolism–immunity nexus	Homo sapiens (human)	Crohn's colitis Crohn's disease anterior uveitis arthritis arthropathy exanthem inflammatory bowel disease 1 inflammatory bowel disease juvenile rheumatoid arthritis pericarditis ulcerative colitis
3906	lactalbumin alpha	LALBA Aliases: HAMLET LYZG LYZL7 lactose synthase B lysozyme G	Homo sapiens (human)	breast cancer breast carcinoma cancer deficiency anemia embryoma eosinophilic esophagitis fibromyalgia gastroenteritis hypochromic anemia liver cirrhosis microcytic anemia milk allergy mitral valve stenosis multiple sclerosis myositis obesity polycystic ovary syndrome steatotic liver disease
10314	LanC like glutathione S-transferase 1	LANCL1	Homo sapiens (human)
55915	LanC like glutathione S-transferase 2	LANCL2	Homo sapiens (human)
347404	LanC like family member 3	LANCL3	Homo sapiens (human)
9215	LARGE xylosyl- and glucuronyltransferase 1	LARGE1 Aliases: KIAA0609 like-acetylglucosaminyltransferase	Homo sapiens (human)	Axenfeld-Rieger syndrome Becker muscular dystrophy Bell's palsy Dandy-Walker syndrome Duchenne muscular dystrophy Fukuyama congenital muscular dystrophy Joubert syndrome Laron syndrome Miller-Dieker lissencephaly syndrome Peters anomaly Walker-Warburg syndrome achondroplasia acoustic neuroma agnosia amphetamine abuse angiomatous meningioma atypical chronic myeloid leukemia, BCR-ABL1 negative autosomal dominant Emery-Dreifuss muscular dystrophy 2 autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy benign meningioma bilateral optic nerve hypoplasia blindness buphthalmos cancer cataract centronuclear myopathy cerebral convexity meningioma chronic monocytic leukemia clear cell meningioma cleft lip cleft palate coloboma communicating hydrocephalus complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 cone-rod dystrophy congenital merosin-deficient muscular dystrophy 1A congenital muscular dystrophy 1B congenital muscular dystrophy due to LMNA mutation congenital muscular dystrophy due to integrin alpha-7 deficiency congenital muscular dystrophy-dystroglycanopathy type A1 congenital muscular dystrophy-dystroglycanopathy type A6 congenital muscular dystrophy congenital myopathy 1A congenital myopathy 4A congenital structural myopathy cornea plana cortical dysplasia-focal epilepsy syndrome cryptorchidism depressive disorder developmental coordination disorder diabetes mellitus dissociated nystagmus distal myopathy endomyocardial fibrosis epilepsy facial nerve disease facial paralysis facioscapulohumeral muscular dystrophy 1 facioscapulohumeral muscular dystrophy familial periodic paralysis fibrous meningioma fundus albipunctatus fundus dystrophy glaucoma hepatocellular carcinoma holoprosencephaly 1 holoprosencephaly hydranencephaly hydrocephalus hydrophthalmos hypertropia idiopathic scoliosis imperforate anus intellectual disability intraorbital meningioma intraventricular meningioma isolated cleft palate isolated elevated serum creatine phosphokinase levels learning disability limb-girdle muscular dystrophy lissencephaly liver cancer lymphoid leukemia lymphoplasmacyte-rich meningioma major depressive disorder mechanical strabismus megaconial type congenital muscular dystrophy megalocornea melancholic depression meningioma meningocele meningothelial meningioma microcephaly microcystic meningioma microphthalmia muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B5 muscular dystrophy-dystroglycanopathy type B6 muscular dystrophy myeloid leukemia myofibrillar myopathy 1 myofibrillar myopathy 3 myopathy myopia nemaline myopathy obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R obsolete melancholia obstructive hydrocephalus oculopharyngeal muscular dystrophy olfactory groove meningioma ophthalmoplegia optic atrophy parasagittal meningioma pathologic nystagmus peripheral retinal degeneration pituitary adenoma pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 psammomatous meningioma recurrent corneal erosion renal agenesis retinal detachment retinitis pigmentosa rhabdomyosarcoma rigid spine muscular dystrophy 1 rippling muscle disease 2 scoliosis secretory meningioma senile degeneration of brain septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly speech disorder spinal meningioma spontaneous ocular nystagmus strabismus syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability Najm type transitional meningioma type 2 diabetes mellitus visual epilepsy
120071	LARGE xylosyl- and glucuronyltransferase 2	LARGE2 Aliases: FLJ35207 PP5656	Homo sapiens (human)	Duchenne muscular dystrophy acute myocardial infarction autosomal dominant Emery-Dreifuss muscular dystrophy 2 autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy cancer congenital muscular dystrophy coronary thrombosis distal myopathy embryoma facioscapulohumeral muscular dystrophy limb-girdle muscular dystrophy muscular dystrophy myocardial infarction myofibrillar myopathy 1 myofibrillar myopathy 3 obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R oculopharyngeal muscular dystrophy prostate cancer prostate carcinoma rippling muscle disease 2 silent myocardial infarction transitional cell carcinoma
143903	layilin	LAYN Aliases: FLJ30977 FLJ31092	Homo sapiens (human)	arthritis arthropathy bronchus cancer bronchus carcinoma cancer chronic obstructive pulmonary disease colitis colon cancer colonic benign neoplasm colorectal cancer embryoma gastroenteritis gliosarcoma glomerulonephritis high grade glioma ileitis ileocolitis kidney disease large intestine cancer lung cancer lung carcinoma mixed glioma nephritis osteoarthritis
3931	lecithin-cholesterol acyltransferase	LCAT Aliases: phosphatidylcholine--sterol O-acyltransferase	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Bloom syndrome Charcot-Marie-Tooth disease X-linked dominant 1 Charcot-Marie-Tooth disease X-linked dominant 6 Charcot-Marie-Tooth disease X-linked recessive 2 Charcot-Marie-Tooth disease X-linked recessive 3 Charcot-Marie-Tooth disease X-linked recessive 4 Charcot-Marie-Tooth disease X-linked recessive 5 Charcot-Marie-Tooth disease axonal type 2C Charcot-Marie-Tooth disease axonal type 2F Charcot-Marie-Tooth disease axonal type 2H Charcot-Marie-Tooth disease axonal type 2K Charcot-Marie-Tooth disease axonal type 2L Charcot-Marie-Tooth disease axonal type 2N Charcot-Marie-Tooth disease axonal type 2O Charcot-Marie-Tooth disease axonal type 2P Charcot-Marie-Tooth disease axonal type 2Q Charcot-Marie-Tooth disease axonal type 2T Charcot-Marie-Tooth disease axonal type 2U Charcot-Marie-Tooth disease dominant intermediate A Charcot-Marie-Tooth disease dominant intermediate B Charcot-Marie-Tooth disease dominant intermediate C Charcot-Marie-Tooth disease dominant intermediate D Charcot-Marie-Tooth disease dominant intermediate E Charcot-Marie-Tooth disease dominant intermediate F Charcot-Marie-Tooth disease recessive intermediate B Charcot-Marie-Tooth disease recessive intermediate C Charcot-Marie-Tooth disease recessive intermediate D Charcot-Marie-Tooth disease type 1A Charcot-Marie-Tooth disease type 1B Charcot-Marie-Tooth disease type 1C Charcot-Marie-Tooth disease type 1D Charcot-Marie-Tooth disease type 1E Charcot-Marie-Tooth disease type 1F Charcot-Marie-Tooth disease type 2 Charcot-Marie-Tooth disease type 2A1 Charcot-Marie-Tooth disease type 2A2A Charcot-Marie-Tooth disease type 2B1 Charcot-Marie-Tooth disease type 2B2 Charcot-Marie-Tooth disease type 2B Charcot-Marie-Tooth disease type 2D Charcot-Marie-Tooth disease type 2E Charcot-Marie-Tooth disease type 2I Charcot-Marie-Tooth disease type 2J Charcot-Marie-Tooth disease type 2R Charcot-Marie-Tooth disease type 2Y Charcot-Marie-Tooth disease type 4A Charcot-Marie-Tooth disease type 4B1 Charcot-Marie-Tooth disease type 4B2 Charcot-Marie-Tooth disease type 4B3 Charcot-Marie-Tooth disease type 4C Charcot-Marie-Tooth disease type 4D Charcot-Marie-Tooth disease type 4E Charcot-Marie-Tooth disease type 4F Charcot-Marie-Tooth disease type 4G Charcot-Marie-Tooth disease type 4H Charcot-Marie-Tooth disease type 4J Charcot-Marie-Tooth disease type 4K Charcot-Marie-Tooth disease Norum disease Pick's disease Reye syndrome Tangier disease abdominal obesity-metabolic syndrome 1 abetalipoproteinemia acute chest syndrome acute myocardial infarction agenesis of the corpus callosum with peripheral neuropathy anemia aortic atherosclerosis arcus senilis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis atrial fibrillation blindness brain stem infarction cardiovascular system disease carotid artery disease cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease cholesterol-ester transfer protein deficiency choreaacanthocytosis chronic kidney disease chylomicron retention disease congestive heart failure corneal dystrophy coronary artery disease coronary thrombosis disease of metabolism dry eye syndrome end stage renal disease familial combined hyperlipidemia familial hypercholesterolemia familial hyperlipidemia familial lipoprotein lipase deficiency familial nephrotic syndrome gallbladder disease glomerulonephritis granular corneal dystrophy heart disease hemolytic anemia hepatocellular carcinoma hereditary neuropathy with liability to pressure palsies hereditary sensory and autonomic neuropathy type 2 hyperalphalipoproteinemia 1 hyperlipoproteinemia type V hypolipoproteinemia inherited metabolic disorder kidney disease kidney failure lipoid nephrosis liver cancer liver disease macrocytic anemia macular corneal dystrophy motor peripheral neuropathy myocardial infarction nephritis nephrosis nephrotic syndrome nutmeg liver obesity obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum ovarian cancer ovarian carcinoma proteinuria pyoureter recurrent corneal erosion renal osteodystrophy rheumatoid arthritis sickle cell anemia silent myocardial infarction steatotic liver disease uremia xerophthalmia
253558	lysocardiolipin acyltransferase 1	LCLAT1 Aliases: 1ysophospholipid acyltransferase 6 AGPAT8 ALCAT1 FLJ37965 LPLAT6 acyl-CoA:lysocardiolipin acyltransferase 1	Homo sapiens (human)	dermatitis idiopathic interstitial pneumonia idiopathic pulmonary fibrosis pneumonia postinflammatory pulmonary fibrosis pulmonary fibrosis
3938	lactase	LCT	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Clostridium difficile colitis Crohn's colitis Crohn's disease EEC syndrome Gilles de la Tourette syndrome Leydig cell tumor Pick's disease Reye syndrome Sertoli cell-only syndrome T-cell acute lymphoblastic leukemia Y-linked spermatogenic failure 1 abdominal obesity-metabolic syndrome 1 acute myocardial infarction acute retinal necrosis syndrome adult T-cell leukemia/lymphoma adult respiratory distress syndrome allergic asthma antiphospholipid syndrome antithrombin III deficiency asthma autoimmune polyendocrine syndrome bullous congenital ichthyosiform erythroderma cancer celiac disease cerebral degeneration colitis colorectal cancer colorectal carcinoma congenital lactase deficiency coronary artery disease coronary thrombosis cystic fibrosis diarrhea dysentery ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 1 ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3 embryoma eosinophilic esophagitis essential hypertension extraosseous Ewing sarcoma extraosseous Ewings sarcoma-primitive neuroepithelial tumor familial adenomatous polyposis 1 familial adenomatous polyposis gastritis gastroenteritis gastrointestinal system disease gestational diabetes gingival recession hypertension ileitis ileocolitis immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome inflammatory bowel disease 1 inflammatory bowel disease intestinal disease intestinal infectious disease intrinsic asthma irritable bowel syndrome islet cell tumor kidney disease kwashiorkor lactic acidosis lactose intolerance large intestine cancer lupus erythematosus marasmus myocardial infarction neurocirculatory asthenia newborn respiratory distress syndrome nutrition disease obesity obsessive-compulsive disorder oligospermia osteomyelitis osteoporosis pneumonia polycystic ovary syndrome prostate cancer prostate carcinoma protein C deficiency protein S deficiency protein-energy malnutrition schizophrenia silent myocardial infarction systemic lupus erythematosus testicular cancer thrombophilia transthyretin amyloidosis tropical sprue ulcerative colitis
197021	lactase like	LCTL Aliases: FLJ33279 KL lactase phlorizin hydrolase KLG KLPH gammaklotho klotho gamma	Homo sapiens (human)	arthritis arthropathy kidney disease osteoarthritis
3939	lactate dehydrogenase A	LDHA	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease B-cell lymphoma Ewing sarcoma Kawasaki disease Kennedy's disease Pick's disease Reye syndrome X-linked dilated cardiomyopathy acoustic neuroma acute myocardial infarction adenocarcinoma adenoma adult hepatocellular carcinoma adult medulloblastoma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis bile duct adenocarcinoma bile duct carcinoma bipolar disorder bladder carcinoma bone osteosarcoma borderline personality disorder brain cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiomyopathy cellular leiomyoma central nervous system cancer central nervous system lymphoma cerebral degeneration cervical adenocarcinoma cervical cancer cervix carcinoma childhood hepatocellular carcinoma childhood leukemia childhood medulloblastoma childhood osteosarcoma cholangiocarcinoma chondrosarcoma chromophobe renal cell carcinoma chronic fatigue syndrome clear cell renal cell carcinoma collecting duct carcinoma colon adenocarcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma coronary artery disease coronary thrombosis cribriform carcinoma cutaneous Paget's disease cystinuria degenerative disc disease depressive disorder diabetes mellitus dilated cardiomyopathy 1AA dilated cardiomyopathy 1B dilated cardiomyopathy 1BB dilated cardiomyopathy 1C dilated cardiomyopathy 1CC dilated cardiomyopathy 1D dilated cardiomyopathy 1DD dilated cardiomyopathy 1E dilated cardiomyopathy 1EE dilated cardiomyopathy 1FF dilated cardiomyopathy 1G dilated cardiomyopathy 1GG dilated cardiomyopathy 1H dilated cardiomyopathy 1HH dilated cardiomyopathy 1I dilated cardiomyopathy 1II dilated cardiomyopathy 1JJ dilated cardiomyopathy 1K dilated cardiomyopathy 1KK dilated cardiomyopathy 1L dilated cardiomyopathy 1M dilated cardiomyopathy 1NN dilated cardiomyopathy 1O dilated cardiomyopathy 1P dilated cardiomyopathy 1Q dilated cardiomyopathy 1R dilated cardiomyopathy 1S dilated cardiomyopathy 1T dilated cardiomyopathy 1U dilated cardiomyopathy 1V dilated cardiomyopathy 1W dilated cardiomyopathy 1X dilated cardiomyopathy 1Y dilated cardiomyopathy 1Z dilated cardiomyopathy 2A dilated cardiomyopathy 2B dilated cardiomyopathy disease of metabolism distal arthrogryposis dysthymic disorder embryoma encephalitis encephalomyelitis endometrial cancer endometrial carcinoma endomyocardial fibrosis esophagus squamous cell carcinoma essential thrombocythemia eye disease familial periodic paralysis familial retinoblastoma fibromyalgia galactosemia gallbladder cancer gallbladder carcinoma gastrointestinal stromal tumor gestational diabetes giant cell glioblastoma glioblastoma gliosarcoma glucosephosphate dehydrogenase deficiency glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease goiter granular cell carcinoma head and neck cancer head and neck squamous cell carcinoma hepatocellular carcinoma high grade glioma hyperglycemia hypertension hypertrophic cardiomyopathy idiopathic interstitial pneumonia idiopathic pulmonary fibrosis impetigo herpetiformis intellectual disability intermittent explosive disorder intrahepatic cholangiocarcinoma isolated elevated serum creatine phosphokinase levels kidney cancer kidney failure kwashiorkor large intestine cancer lateral meningocele syndrome learning disability leukemia liver cancer liver cirrhosis lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung squamous cell carcinoma lymphoma major depressive disorder marasmus medulloblastoma medullomyoblastoma melancholic depression melanoma melanotic medulloblastoma meningioma middle cerebral artery infarction mixed glioma mood disorder multiple myeloma multiple sclerosis myelitis myelofibrosis myocardial infarction myoglobinuria myopathy myositis nasopharynx carcinoma neuroblastoma neurotic disorder nodular prostate nonpapillary renal cell carcinoma nontoxic goiter nutrition disease obsolete melancholia obsolete ymphosarcoma osteosarcoma ovarian cancer ovarian carcinoma oxyphilic adenoma pancreatic cancer pancreatic carcinoma panic disorder papillary adenocarcinoma papillary renal cell carcinoma peptic ulcer disease pituitary adenoma pituitary cancer pituitary carcinoma postinflammatory pulmonary fibrosis prostate cancer prostate carcinoma prostatic adenoma protein-energy malnutrition pseudosarcomatous fibromatosis pulmonary fibrosis renal carcinoma renal cell carcinoma renal oncocytoma retinoblastoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma silent myocardial infarction skin melanoma stomach cancer stomach carcinoma thyroid adenoma thyroid cancer thyroid gland anaplastic carcinoma thyroid gland carcinoma thyroid gland disease thyroid gland papillary carcinoma trilateral retinoblastoma tubular adenocarcinoma type 2 diabetes mellitus urinary bladder cancer uterine corpus cancer uterine corpus sarcoma viral infectious disease
160287	lactate dehydrogenase A like 6A	LDHAL6A Aliases: LDH6A MGC23940	Homo sapiens (human)	disease of metabolism
92483	lactate dehydrogenase A like 6B	LDHAL6B Aliases: LDH6B LDHL	Homo sapiens (human)	breast cancer breast carcinoma disease of metabolism

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