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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 **392976 - 393000** of **393515** in total

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Gene ID ▼	Gene Name	Gene Symbol	Organism	Disease Ontology
5509	protein phosphatase 1 regulatory subunit 3D	PPP1R3D	Homo sapiens (human)
5507	protein phosphatase 1 regulatory subunit 3C	PPP1R3C Aliases: PTG Phosphatase 1, regulatory inhibitor subunit 5 protein targeting to glycogen	Homo sapiens (human)	alcohol use disorder antithrombin III deficiency breast cancer cancer colorectal cancer colorectal carcinoma depressive disorder diabetes mellitus dysthymic disorder embryoma head and neck cancer hepatocellular carcinoma large intestine cancer liver cancer major depressive disorder melancholic depression neurotic disorder obsolete melancholia post-traumatic stress disorder protein C deficiency protein S deficiency steatotic liver disease thrombophilia type 2 diabetes mellitus
5506	protein phosphatase 1 regulatory subunit 3A	PPP1R3A Aliases: GM glycogen-associated regulatory subunit of protein phosphatase-1 protein phosphatase 1 regulatory subunit GM	Homo sapiens (human)	Alzheimer's disease adult lymphoma atrial fibrillation atypical chronic myeloid leukemia, BCR-ABL1 negative breast cancer cancer carcinoma central nervous system lymphoma childhood lymphoma chronic monocytic leukemia colorectal cancer colorectal carcinoma communication disorder congestive heart failure diabetes mellitus diabetic ketoacidosis embryoma glucose intolerance hematologic cancer hypoglycemia language disorder large intestine cancer laryngeal squamous cell carcinoma lymphoid leukemia lymphoma myeloid leukemia obsolete ymphosarcoma prediabetes syndrome prostate cancer prostate carcinoma sarcomatoid carcinoma type 2 diabetes mellitus
5504	protein phosphatase 1 regulatory inhibitor subunit 2	PPP1R2	Homo sapiens (human)
5502	protein phosphatase 1 regulatory inhibitor subunit 1A	PPP1R1A	Homo sapiens (human)
5501	protein phosphatase 1 catalytic subunit gamma	PPP1CC	Homo sapiens (human)	cancer congestive heart failure type 2 diabetes mellitus
5500	protein phosphatase 1 catalytic subunit beta	PPP1CB	Homo sapiens (human)	Noonan syndrome-like disorder with loose anagen hair 2 cancer
5499	protein phosphatase 1 catalytic subunit alpha	PPP1CA	Homo sapiens (human)	cancer type 2 diabetes mellitus
5476	cathepsin A	CTSA Aliases: carboxypeptidase C carboxypeptidase Y-like kininase carboxypeptidase-L deamidase lysosomal carboxypeptidase A lysosomal protective protein urinary kininase	Homo sapiens (human)	CADASIL 1 CADASIL Fabry disease GM1 gangliosidosis type 1 GM1 gangliosidosis Laron syndrome abdominal aortic aneurysm achondroplasia acquired immunodeficiency syndrome adult-onset leukoencephalopathy with axonal spheroids and pigmented glia allergic asthma aortic aneurysm aortic valve disease 2 aortic valve stenosis aspartylglucosaminuria asthma bone giant cell tumor cancer cavernous hemangioma chorioangioma chylomicron retention disease colitis colorectal cancer colorectal carcinoma corneal dystrophy embryoma epilepsy essential hypertension fucosidosis galactosialidosis gastroenteritis genital herpes glomus tumor glycoproteinosis hemangioma herpes simplex histiocytoid hemangioma human immunodeficiency virus infectious disease hyperglycemia hypertension idiopathic interstitial pneumonia idiopathic pulmonary fibrosis ileitis ileocolitis inflammatory breast carcinoma intellectual disability intramuscular hemangioma intrinsic asthma invasive ductal carcinoma kidney failure large intestine cancer learning disability lipid storage disease lung adenocarcinoma lung cancer lymphangioma lysosomal storage disease mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis type IVB mucopolysaccharidosis multiple epiphyseal dysplasia oophoritis osteochondrodysplasia parametritis pelvic inflammatory disease pneumonia pyosalpinx recurrent corneal erosion salpingitis sensorineural hearing loss shigellosis steatotic liver disease uremia visual epilepsy
5471	phosphoribosyl pyrophosphate amidotransferase	PPAT Aliases: GPAT PRAT	Homo sapiens (human)	alcohol dependence alcohol use disorder breast cancer chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma hepatoblastoma hepatocellular carcinoma liver cancer ovarian cancer ovarian carcinoma papillary renal cell carcinoma renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma stomach cancer stomach carcinoma
5467	peroxisome proliferator activated receptor delta	PPARD	Homo sapiens (human)	biliary tract cancer pancreatic cancer type 2 diabetes mellitus
5465	peroxisome proliferator activated receptor alpha	PPARA	Homo sapiens (human)	Alzheimer's disease alcoholic hepatitis coronary artery disease cystic fibrosis hepatocellular carcinoma hydrocephalus hypertension hypertensive encephalopathy lipid metabolism disorder myocardial infarction obesity periodontitis schizophrenia steatotic liver disease
5408	pancreatic lipase related protein 2 (gene/pseudogene)	PNLIPRP2 Aliases: PLRP2	Homo sapiens (human)	acute pancreatitis pancreatitis
5407	pancreatic lipase related protein 1	PNLIPRP1 Aliases: PLRP1	Homo sapiens (human)	breast cancer prostate cancer
5406	pancreatic lipase	PNLIP Aliases: PL triacylglycerol lipase	Homo sapiens (human)	acute myeloid leukemia acute pancreatitis cancer central nervous system cancer diabetes mellitus gliosarcoma high grade glioma mixed glioma obesity obsolete steatorrhea pancreatic cancer pancreatic carcinoma pancreatitis thrombocytopenia tropical sprue type 2 diabetes mellitus
5373	phosphomannomutase 2	PMM2 Aliases: CDG1a CDGS Congenital disorder of glycosylation, type Ia PMI PMI1 mannose-6-phosphate isomerase phosphomannose isomerase 1	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 Dandy-Walker syndrome Duchenne muscular dystrophy Hailey-Hailey disease Kallmann syndrome Marfan syndrome Meckel syndrome Pick's disease Reye syndrome Rothmund-Thomson syndrome Sheehan syndrome West syndrome Zollinger-Ellison syndrome acute myeloid leukemia acute myocardial infarction androgen insensitivity syndrome antithrombin III deficiency anxiety disorder aspiration pneumonia aspiration pneumonitis autosomal dominant Emery-Dreifuss muscular dystrophy 2 autosomal dominant cutis laxa 1 autosomal dominant cutis laxa 2 autosomal dominant cutis laxa 3 autosomal dominant cutis laxa 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 dominant polycystic kidney disease autosomal recessive chronic granulomatous disease 1 autosomal recessive cutis laxa type IA autosomal recessive cutis laxa type IB autosomal recessive cutis laxa type II classic type autosomal recessive cutis laxa type IIA autosomal recessive cutis laxa type IIB autosomal recessive cutis laxa type IIC autosomal recessive cutis laxa type IID autosomal recessive cutis laxa type IIIA autosomal recessive cutis laxa type IIIB 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 blindness brain ischemia cancer cardiomyopathy cardiovascular system disease cataract cerebellar ataxia cerebellar disease cerebral degeneration cerebral palsy chronic granulomatous disease clubfoot coloboma of optic nerve colorectal cancer colorectal carcinoma cone-rod dystrophy congenital diaphragmatic hernia congenital disorder of glycosylation Ia congenital disorder of glycosylation Ib congenital disorder of glycosylation Id congenital disorder of glycosylation Ie congenital disorder of glycosylation In congenital disorder of glycosylation Iq congenital disorder of glycosylation type I congenital disorder of glycosylation congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 congenital hypothyroidism congenital muscular dystrophy congenital nystagmus coronary thrombosis critical illness polyneuropathy cryptorchidism cutis laxa cystic kidney disease developmental and epileptic encephalopathy 36 diabetes mellitus diabetic autonomic neuropathy diabetic ketoacidosis diabetic neuropathy diabetic polyneuropathy diarrhea disease of metabolism dissociated nystagmus distal myopathy egg allergy elephantiasis embryoma endomyocardial fibrosis epilepsy esotropia essential hypertension facioscapulohumeral muscular dystrophy familial hemiplegic migraine 1 familial hemiplegic migraine familial hyperinsulinemic hypoglycemia 1 familial hyperinsulinemic hypoglycemia 2 familial hypertrophic cardiomyopathy familial nephrotic syndrome fundus albipunctatus gallbladder disease generalized anxiety disorder heart disease hemiplegia hemopericardium hyperinsulinemic hypoglycemia hyperinsulinism hypertension hypertrophic cardiomyopathy hypertropia hypogonadism 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 hypothyroidism inflammatory and toxic neuropathy inherited metabolic disorder intellectual disability 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 large intestine cancer learning disability limb-girdle muscular dystrophy lingual-facial-buccal dyskinesia lipoatrophic diabetes mellitus lipodystrophy lipoid nephrosis liver cirrhosis liver disease lung adenocarcinoma lung cancer lymphedema mal de Meleda marasmus mechanical strabismus meningoencephalitis microcephaly migraine with aura monocular esotropia movement disease muscular dystrophy myocardial infarction myofibrillar myopathy 1 myofibrillar myopathy 3 myopia myxedema nephrotic syndrome neuropathy non-congenital cyst of kidney 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 infantile epileptic encephalopathy oculopharyngeal muscular dystrophy olivopontocerebellar atrophy open-angle glaucoma ophthalmoplegia osteoporosis panhypopituitarism pathologic nystagmus pericardial effusion pericarditis peripheral nervous system disease periventricular leukomalacia phobic disorder polyhydramnios polyneuropathy premature menopause primary open angle glaucoma primary ovarian insufficiency protein C deficiency protein S deficiency proteinuria pulmonary valve stenosis restrictive dermopathy retinitis pigmentosa rippling muscle disease 2 schizophrenia scoliosis silent myocardial infarction situs inversus spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy spontaneous ocular nystagmus steatotic liver disease strabismus thrombocytopenia thrombocytosis thrombophilia tuberous sclerosis type 2 diabetes mellitus visual epilepsy visual pathway disease
5372	phosphomannomutase 1	PMM1 Aliases: Sec53 brain glucose-1,6-bisphosphatase	Homo sapiens (human)	congenital disorder of glycosylation Ia congenital disorder of glycosylation type I hepatitis
5338	phospholipase D2	PLD2 Aliases: choline phosphatase 2	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 Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome abdominal obesity-metabolic syndrome 1 actinic keratosis amnestic disorder anaplastic astrocytoma anodontia basal cell carcinoma brain infarction breast cancer breast carcinoma cancer carcinoma central nervous system cancer central nervous system lymphoma cerebral degeneration childhood cerebral astrocytoma chromophobe renal cell carcinoma chronic kidney disease clear cell renal cell carcinoma colitis collecting duct carcinoma colon adenocarcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma complex partial epilepsy congestive heart failure developmental cardiac valvular defect embryoma epilepsy epithelioid sarcoma essential hypertension fibrillary astrocytoma gastroenteritis gemistocytic astrocytoma giant cell glioblastoma glioblastoma gliosarcoma high grade glioma hypertension ileitis ileocolitis in situ carcinoma inverted follicular keratosis juvenile pilocytic astrocytoma keratoacanthoma kwashiorkor large intestine cancer lymphoid leukemia lymphoma malignant astrocytoma marasmus melanoacanthoma mixed glioma myeloid leukemia nonpapillary renal cell carcinoma nutrition disease obsolete ymphosarcoma papillary adenocarcinoma papillary renal cell carcinoma penis carcinoma in situ pilocytic astrocytoma pneumonia prostate cancer prostate carcinoma protein-energy malnutrition protoplasmic astrocytoma renal carcinoma renal cell carcinoma retinal disease retinitis retrograde amnesia sarcoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma seborrheic keratosis skin disease spindle cell sarcoma squamous cell carcinoma subependymal giant cell astrocytoma systemic lupus erythematosus temporal lobe epilepsy thyroid gland papillary carcinoma tongue squamous cell carcinoma tooth agenesis vascular cancer visual epilepsy
5337	phospholipase D1	PLD1 Aliases: choline phosphatase 1	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 Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome acral lentiginous melanoma acute myocardial infarction adult respiratory distress syndrome allergic asthma amnestic disorder anaplastic astrocytoma arthritis arthropathy asthma atrial heart septal defect 1 atrial heart septal defect 2 atrial heart septal defect 3 atrial heart septal defect 4 atrial heart septal defect 5 atrial heart septal defect 6 atrial heart septal defect 7 atrial heart septal defect 8 atrial heart septal defect 9 atrial heart septal defect autoimmune disease autoimmune lymphoproliferative syndrome bacterial sepsis bone osteosarcoma brain infarction breast cancer breast carcinoma cancer candidiasis carcinoma central nervous system cancer cerebral degeneration childhood cerebral astrocytoma childhood osteosarcoma chromophobe renal cell carcinoma chronic kidney disease clear cell renal cell carcinoma colitis collecting duct carcinoma colorectal cancer colorectal carcinoma complex partial epilepsy congestive heart failure coronary thrombosis dementia developmental cardiac valvular defect diabetes mellitus disseminated intravascular coagulation embryoma epilepsy fibrillary astrocytoma gastroenteritis gemistocytic astrocytoma gliosarcoma high grade glioma hydronephrosis ileitis ileocolitis immune system disease inguinal hernia intrinsic asthma juvenile pilocytic astrocytoma large intestine cancer malignant astrocytoma melanoma microphthalmia middle cerebral artery infarction mitral valve insufficiency mitral valve prolapse mitral valve stenosis mixed glioma multiple sclerosis myocardial infarction newborn respiratory distress syndrome nodular prostate nonpapillary renal cell carcinoma obesity obsolete Matthew-Wood syndrome oral candidiasis osteosarcoma pancreatic ductal adenocarcinoma papillary renal cell carcinoma patent foramen ovale pilocytic astrocytoma pneumonia postural orthostatic tachycardia syndrome primary immunodeficiency disease prostate cancer prostate carcinoma prostatic adenoma protoplasmic astrocytoma pterygium purpura fulminans relapsing-remitting multiple sclerosis renal carcinoma renal cell carcinoma retrograde amnesia rheumatoid arthritis sarcomatoid carcinoma sarcomatoid renal cell carcinoma silent myocardial infarction skin melanoma stomach cancer stomach carcinoma subependymal giant cell astrocytoma temporal lobe epilepsy tricuspid atresia tricuspid valve insufficiency tricuspid valve prolapse type 2 diabetes mellitus urethral diverticulum visual epilepsy
5336	phospholipase C gamma 2	PLCG2	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 Burkitt lymphoma CINCA Syndrome Creutzfeldt-Jakob disease Crohn's colitis Crohn's disease Hailey-Hailey disease Lewy body dementia Muckle-Wells syndrome Pick's disease Reye syndrome Richter's syndrome Rothmund-Thomson syndrome acute lymphoblastic leukemia acute myeloid leukemia adenosarcoma age related macular degeneration allergic rhinitis angioedema autoimmune disease autoimmune lymphoproliferative syndrome autoimmune thyroiditis autosomal dominant cutis laxa 1 autosomal dominant cutis laxa 2 autosomal dominant cutis laxa 3 autosomal dominant cutis laxa autosomal recessive cutis laxa type IA autosomal recessive cutis laxa type IB autosomal recessive cutis laxa type II classic type autosomal recessive cutis laxa type IIA autosomal recessive cutis laxa type IIB autosomal recessive cutis laxa type IIC autosomal recessive cutis laxa type IID autosomal recessive cutis laxa type IIIA autosomal recessive cutis laxa type IIIB bone osteosarcoma breast cancer breast carcinoma bronchiolitis cancer candidiasis cellulitis central nervous system lymphoma cerebral degeneration cherubism childhood osteosarcoma childhood type dermatomyositis chronic lymphocytic leukemia coronary artery disease cutis laxa degeneration of macula and posterior pole dermatomyositis diffuse large B-cell lymphoma embryoma exostosis familial adenomatous polyposis 1 familial adenomatous polyposis familial cold autoinflammatory syndrome 1 familial cold autoinflammatory syndrome 3 familial cold autoinflammatory syndrome 4 familial cold autoinflammatory syndrome granuloma annulare hepatocellular carcinoma immune system disease inflammatory bowel disease 1 inflammatory bowel disease interstitial lung disease islet cell tumor kidney cancer leukemia lipoid nephrosis liver cancer lymphoma lymphoplasmacytic lymphoma macroglobulinemia macular degeneration mal de Meleda nephroblastoma neurodegenerative disease obsolete lymphoplasmacytic lymphoma obsolete ymphosarcoma oral candidiasis osteoporosis osteosarcoma progressive supranuclear palsy restrictive dermopathy rheumatoid arthritis stomach cancer thrombophilia ulcerative colitis urticaria vasomotor rhinitis vitiligo
5335	phospholipase C gamma 1	PLCG1 Aliases: NCKAP3 PLC-II PLC148 PLCgamma1	Homo sapiens (human)	Alzheimer's disease Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Kaposi's sarcoma Meckel syndrome Miller-Dieker lissencephaly syndrome Richter's syndrome SADDAN Sezary's disease T-cell acute lymphoblastic leukemia X-linked lymphoproliferative syndrome 1 X-linked lymphoproliferative syndrome 2 abdominal obesity-metabolic syndrome 1 achondroplasia acute monocytic leukemia acute myeloid leukemia acute myocardial infarction adenocarcinoma adenoma adult T-cell leukemia/lymphoma allergic asthma angioedema angioimmunoblastic T-cell lymphoma angiosarcoma arteriosclerotic cardiovascular disease arthritis arthropathy asthma atherosclerosis atrial fibrillation autosomal dominant polycystic kidney disease bacterial sepsis bipolar disorder bone osteosarcoma borderline personality disorder breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer candidiasis carcinoma central nervous system cancer cerebral infarction cerebrovascular disease childhood angiosarcoma childhood osteosarcoma chromosome 17p13.1 deletion syndrome chronic lymphocytic leukemia colitis colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congestive heart failure coronary artery disease cribriform carcinoma depressive disorder diabetes mellitus diabetic ketoacidosis embryoma epilepsy essential hypertension essential thrombocythemia familial adenomatous polyposis focal segmental glomerulosclerosis fragile X syndrome gastric adenocarcinoma gastroenteritis giant cell glioblastoma glioblastoma gliosarcoma glycoproteinosis granular cell carcinoma hepatocellular carcinoma high grade glioma hypertension ileitis ileocolitis immune system disease impulse control disorder intermittent explosive disorder intrinsic asthma irritant dermatitis kleptomania large intestine cancer laryngeal squamous cell carcinoma leukemia lissencephaly liver angiosarcoma liver cancer luminal breast carcinoma A lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma major depressive disorder maturity-onset diabetes of the young melancholic depression mixed glioma mucolipidosis II alpha/beta myelodysplastic syndrome obsolete melancholia oral candidiasis oral squamous cell carcinoma osteoarthritis osteosarcoma ovarian cancer ovarian carcinoma placental insufficiency primary cutaneous T-cell non-Hodgkin lymphoma prostate cancer prostate carcinoma sarcomatoid carcinoma schizophrenia squamous cell carcinoma steatotic liver disease tongue squamous cell carcinoma tubular adenocarcinoma type 2 diabetes mellitus urticaria visual epilepsy
5333	phospholipase C delta 1	PLCD1 Aliases: 1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase delta-1 Phospholipase C δ1	Homo sapiens (human)	Alzheimer's disease Marfan syndrome actinic keratosis alopecia amyotrophic lateral sclerosis arthritis arthropathy blepharitis breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma chronic myeloid leukemia colorectal cancer colorectal carcinoma congestive heart failure coronary artery disease coronary artery vasospasm cystic fibrosis diabetes mellitus embryoma esophagus squamous cell carcinoma essential hypertension glycoproteinosis hypertension impulse control disorder intermittent explosive disorder irritant dermatitis kleptomania large intestine cancer lung benign neoplasm lung cancer lung carcinoma microphthalmia mucolipidosis II alpha/beta nephrolithiasis nonsyndromic congenital nail disorder 3 obsolete Matthew-Wood syndrome obsolete asthenopia osteoarthritis parapsoriasis progressive muscular atrophy psoriasis pustulosis of palm and sole sarcomatoid carcinoma seborrheic keratosis situs inversus skin disease squamous cell carcinoma stomach cancer stomach carcinoma tongue squamous cell carcinoma tuberous sclerosis 1 tuberous sclerosis type 2 diabetes mellitus uric acid nephrolithiasis
5332	phospholipase C beta 4	PLCB4	Homo sapiens (human)	46,XY sex reversal Chagas disease 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 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 3 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 Kawasaki disease abdominal obesity-metabolic syndrome 1 absence epilepsy acute chest syndrome acute myeloid leukemia adenocarcinoma adenoma agenesis of the corpus callosum with peripheral neuropathy agnosia ankylosis bipolar disorder breast cancer breast carcinoma cancer central sleep apnea childhood absence epilepsy childhood acute myeloid leukemia cleft palate congenital ptosis coronary aneurysm cribriform carcinoma cutaneous fibrous histiocytoma dengue hemorrhagic fever depressive disorder embryoma endometriosis of uterus endometriosis essential thrombocythemia gastrointestinal stromal tumor granular cell carcinoma hereditary neuropathy with liability to pressure palsies hidradenoma isolated cleft palate lung cancer lung non-small cell carcinoma major depressive disorder melancholic depression melanoma mood disorder motor peripheral neuropathy myelodysplastic syndrome neurotic disorder nicotine dependence obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum obsolete melancholia obstructive sleep apnea ptosis retinal degeneration retinal disease schizoaffective disorder schizophrenia schizophreniform disorder sensorineural hearing loss skin melanoma skin papilloma skin tag syringoma tongue disease trypanosomiasis tubular adenocarcinoma uveal melanoma
5331	phospholipase C beta 3	PLCB3	Homo sapiens (human)	acrodermatitis acute myocardial infarction adenocarcinoma adenoma adrenal carcinoma adrenal cortex cancer adrenocortical carcinoma cancer coronary thrombosis cribriform carcinoma cystic fibrosis dermatitis diabetes mellitus diabetic ketoacidosis essential hypertension extragonadal germ cell cancer granular cell carcinoma hyperparathyroidism hypertension lung cancer lung disease lung non-small cell carcinoma multiple endocrine neoplasia type 1 myocardial infarction neuroendocrine carcinoma neuroendocrine tumor obesity osteitis fibrosa silent myocardial infarction spondylometaphyseal dysplasia with corneal dystrophy tubular adenocarcinoma type 2 diabetes mellitus vitiligo
5330	phospholipase C beta 2	PLCB2 Aliases: FLJ38135	Homo sapiens (human)	acute myocardial infarction adenocarcinoma adenoma breast cancer breast carcinoma cancer congenital heart disease coronary thrombosis cribriform carcinoma embryoma granular cell carcinoma hepatocellular carcinoma invasive ductal carcinoma liver cancer melanoma myocardial infarction obesity silent myocardial infarction skin melanoma tubular adenocarcinoma viral infectious disease

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