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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	October 29, 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 **8051 - 8075** of **9988** in total

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Gene ID	Gene Name	Gene Symbol ▲	Organism	Disease Ontology
55315	solute carrier family 29 member 3	SLC29A3	Homo sapiens (human)
222962	solute carrier family 29 member 4	SLC29A4	Homo sapiens (human)
6513	solute carrier family 2 member 1	SLC2A1	Homo sapiens (human)	Alzheimer's disease Hirschsprung's disease carbohydrate metabolic disorder childhood absence epilepsy childhood onset GLUT1 deficiency syndrome 2 diabetes mellitus dystonia 9 hemangioma hypertension hypothyroidism idiopathic generalized epilepsy 12 middle cerebral artery infarction myelomeningocele nephroblastoma obesity pre-eclampsia type 2 diabetes mellitus
81031	solute carrier family 2 member 10	SLC2A10 Aliases: GLUT-10 GLUT10 facilitative glucose transporter GLUT10	Homo sapiens (human)	Hailey-Hailey disease Legg-Calve-Perthes disease Loeys-Dietz syndrome Moyamoya disease Rothmund-Thomson syndrome X-linked dilated cardiomyopathy acute myocardial infarction adenocarcinoma adenoma adult respiratory distress syndrome allergic asthma aortic aneurysm aortic valve disease 2 aortic valve insufficiency aortic valve stenosis arterial tortuosity syndrome asthma 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 blepharophimosis bone disease breast cancer breast carcinoma bronchiolo-alveolar adenocarcinoma bronchus cancer bronchus carcinoma cancer cardiac arrest cardiomyopathy cartilage disease cataract 32 multiple types cerebral infarction cerebrovascular disease childhood type dermatomyositis chondrosarcoma collagen disease congenital central hypoventilation syndrome congenital diaphragmatic hernia congestive heart failure connective tissue disease corneal disease coronary thrombosis craniosynostosis cribriform carcinoma cutis laxa dermatomyositis diabetes mellitus diabetic ketoacidosis 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 endomyocardial fibrosis esophagitis essential hypertension familial hypertrophic cardiomyopathy gastroesophageal reflux disease granular cell carcinoma hiatus hernia hypertension hypertrophic cardiomyopathy hypertropia idiopathic interstitial pneumonia idiopathic pulmonary fibrosis inguinal hernia intellectual disability intermittent claudication interstitial lung disease intrinsic asthma keratoconus learning disability leukocyte adhesion deficiency 1 leukocyte adhesion deficiency lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma mal de Meleda mechanical strabismus megalocornea myocardial infarction myocarditis myopia newborn respiratory distress syndrome obstructive lung disease omphalocele ophthalmoplegia peptic esophagitis peripheral artery disease peripheral vascular disease pneumonia pulmonary emphysema pyloric stenosis respiratory failure restrictive dermopathy scoliosis silent myocardial infarction strabismus thoracic aortic aneurysm tubular adenocarcinoma type 2 diabetes mellitus umbilical hernia vascular disease
66035	solute carrier family 2 member 11	SLC2A11	Homo sapiens (human)
154091	solute carrier family 2 member 12	SLC2A12 Aliases: GLUT12 GLUT8	Homo sapiens (human)	amyloidosis breast cancer cancer congenital hypothyroidism coronary artery disease diabetic ketoacidosis hypothyroidism multiple myeloma myxedema obsolete type 1 diabetes mellitus 9 prostate cancer prostate carcinoma steatotic liver disease 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 type 2 diabetes mellitus
114134	solute carrier family 2 member 13	SLC2A13	Homo sapiens (human)
144195	solute carrier family 2 member 14	SLC2A14	Homo sapiens (human)
6514	solute carrier family 2 member 2	SLC2A2 Aliases: GLUT-2	Homo sapiens (human)	B-cell lymphoma Fanconi syndrome Laron syndrome X-linked dominant hypophosphatemic rickets abdominal obesity-metabolic syndrome 1 achondroplasia atopic dermatitis breast cancer breast carcinoma cancer carcinoma cardiovascular system disease chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer cystinosis cystinuria dental caries dentin caries dermatitis diabetes mellitus diabetic ketoacidosis disease of metabolism embryoma essential hypertension familial adenomatous polyposis galactokinase deficiency galactosemia gastrinoma gestational diabetes glomerulonephritis glucose intolerance glucose metabolism disease 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 heart disease hepatitis C hepatocellular carcinoma hyperglycemia hypertension hypoglycemia hypokalemia hypophosphatemia insulinoma intestinal atresia islet cell tumor kidney disease kidney failure lactic acidosis large intestine cancer liver cancer lung squamous cell carcinoma maturity-onset diabetes of the young melanoma myelomeningocele neonatal diabetes nephritis nephrosis obesity obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma osteomalacia oxyphilic adenoma papillary renal cell carcinoma permanent neonatal diabetes mellitus placental insufficiency prediabetes syndrome pyoureter renal carcinoma renal cell carcinoma renal glycosuria renal oncocytoma rickets sarcomatoid carcinoma sarcomatoid renal cell carcinoma skin melanoma spondyloepimetaphyseal dysplasia, Sponastrime type squamous cell carcinoma steatotic liver disease tethered spinal cord syndrome tongue squamous cell carcinoma transient neonatal diabetes mellitus tropical sprue 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 type 2 diabetes mellitus viral infectious disease
6515	solute carrier family 2 member 3	SLC2A3	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 Fabry disease Graves' disease Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Peutz-Jeghers syndrome Pick's disease Reye syndrome Wolman disease Zollinger-Ellison syndrome acanthosis nigricans acute myeloid leukemia adenocarcinoma adenoma adenosarcoma adult lymphoma allergic contact dermatitis anaplastic astrocytoma arteriosclerotic cardiovascular disease atherosclerosis atrial fibrillation attention deficit hyperactivity disorder autism spectrum disorder autistic disorder autoimmune hepatitis bladder carcinoma brain cancer brain disease breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cataract central nervous system cancer central nervous system lymphoma cerebral degeneration childhood cerebral astrocytoma childhood lymphoma choriocarcinoma chromophobe renal cell carcinoma chylomicron retention disease clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital heart disease congenital hypothyroidism coronary artery disease cribriform carcinoma dementia dermoid cyst of ovary diabetes mellitus diabetic ketoacidosis embryoma embryonal cancer endometrial cancer endometrial carcinoma endometriosis of uterus endometriosis epilepsy essential hypertension familial adenomatous polyposis fibrillary astrocytoma follicular adenoma gemistocytic astrocytoma germ cell and embryonal cancer germ cell cancer germinoma gestational diabetes giant cell glioblastoma glioblastoma gliosarcoma glucose intolerance granular cell carcinoma head and neck squamous cell carcinoma hepatocellular carcinoma high grade glioma hyperglycemia hyperinsulinism hypertension hyperthyroidism hypoglycemia hypothyroidism idiopathic generalized epilepsy inflammatory bowel disease insulinoma islet cell tumor juvenile pilocytic astrocytoma juvenile rheumatoid arthritis large cell carcinoma large intestine cancer laryngeal benign neoplasm laryngeal carcinoma larynx cancer lingual-facial-buccal dyskinesia lipid storage disease liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoma malignant astrocytoma melanoma microcystic adenoma middle cerebral artery infarction mixed glioma movement disease myelomeningocele myxedema nephroblastoma neuroblastoma nevoid basal cell carcinoma syndrome obesity obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma ovarian cancer ovarian carcinoma papillary adenocarcinoma papillary adenoma papillary carcinoma papillary renal cell carcinoma pilocytic astrocytoma placenta cancer placental insufficiency prediabetes syndrome prostate cancer prostate carcinoma protoplasmic astrocytoma renal carcinoma renal cell carcinoma rheumatoid arthritis sarcomatoid renal cell carcinoma schizophrenia skin melanoma squamous cell carcinoma subependymal giant cell astrocytoma tethered spinal cord syndrome thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland follicular carcinoma thyroid gland papillary carcinoma thyrotoxicosis tongue squamous cell carcinoma tuberculosis tubular adenocarcinoma 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 type 2 diabetes mellitus urinary bladder cancer uterine corpus cancer visual epilepsy von Hippel-Lindau disease
6517	solute carrier family 2 member 4	SLC2A4	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 Creutzfeldt-Jakob disease Graves' disease Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Richter's syndrome Simpson-Golabi-Behmel syndrome type 1 X-linked dilated cardiomyopathy Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 acute myocardial infarction adenocarcinoma adenoma alternating hemiplegia of childhood alveolar rhabdomyosarcoma amnestic disorder anterolateral myocardial infarction anteroseptal myocardial infarction autonomic neuropathy bacterial sepsis bone osteosarcoma breast cancer breast carcinoma cancer cardiovascular system disease central nervous system disease centronuclear myopathy cerebral degeneration childhood osteosarcoma chromophobe renal cell carcinoma chronic kidney disease chronic lymphocytic leukemia chronic obstructive pulmonary disease clear cell adenocarcinoma clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital structural myopathy congestive heart failure coronary artery disease coronary thrombosis cribriform carcinoma dental caries dentin caries depressive disorder dermoid cyst of ovary diabetes mellitus diabetic ketoacidosis dilated cardiomyopathy 1A 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 dysthymic disorder embryoma endometrial cancer endometrial carcinoma endometriosis of uterus endometriosis essential hypertension familial hyperlipidemia gastrointestinal stromal tumor gestational diabetes gingival fibromatosis glucose intolerance glycogen storage disease Ia glycogen storage disease V granular cell carcinoma head and neck squamous cell carcinoma heart disease hepatocellular carcinoma hyperglycemia hyperinsulinism hypertension hyperthyroidism hypoglycemia kwashiorkor large intestine cancer leiomyoma liver cancer liver carcinoma liver cirrhosis major depressive disorder marasmus melancholic depression mitral valve stenosis morbid obesity multiple myeloma multiple sclerosis myocardial infarction myofibroma myotonic dystrophy type 1 myotonic dystrophy type 2 nervous system disease neuropathy neurotic disorder nonpapillary renal cell carcinoma nutrition disease obesity obsolete melancholia obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma obstructive sleep apnea osteosarcoma ovarian cancer ovarian carcinoma oxyphilic adenoma papillary renal cell carcinoma periodontal disease periodontitis peripheral nervous system disease placental insufficiency polycystic ovary syndrome polyneuropathy prediabetes syndrome primary pulmonary hypertension prostate cancer prostate carcinoma protein-energy malnutrition psoriatic arthritis pulmonary hypertension renal agenesis renal carcinoma renal cell carcinoma renal oncocytoma sarcomatoid renal cell carcinoma silent myocardial infarction squamous cell carcinoma steatotic liver disease stomach cancer stomach carcinoma systemic lupus erythematosus thyrotoxicosis tongue squamous cell carcinoma tubular adenocarcinoma 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 type 2 diabetes mellitus uterine corpus cancer uterine fibroid vascular disease
6518	solute carrier family 2 member 5	SLC2A5	Homo sapiens (human)	abdominal obesity-metabolic syndrome 1 acute myeloid leukemia breast cancer breast carcinoma cancer central nervous system cancer childhood B-cell acute lymphoblastic leukemia chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colon adenocarcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer diabetes mellitus disease of metabolism embryoma essential hypertension gliosarcoma hepatocellular carcinoma high grade glioma hypertension idiopathic interstitial pneumonia idiopathic pulmonary fibrosis inflammatory bowel disease intestinal atresia large intestine cancer liver cancer long QT syndrome lung adenocarcinoma lung benign neoplasm lung cancer lung non-small cell carcinoma mixed glioma neuroblastoma nonpapillary renal cell carcinoma obesity ovarian cancer ovarian carcinoma papillary renal cell carcinoma prostate cancer prostate carcinoma renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma seminoma testicular cancer testicular germ cell cancer testis seminoma tropical sprue type 2 diabetes mellitus
11182	solute carrier family 2 member 6	SLC2A6	Homo sapiens (human)
155184	solute carrier family 2 member 7	SLC2A7	Homo sapiens (human)
29988	solute carrier family 2 member 8	SLC2A8 Aliases: GLUT8 GLUTX1	Homo sapiens (human)	cancer congenital hypothyroidism diabetic ketoacidosis hypothyroidism multiple myeloma myxedema obsolete type 1 diabetes mellitus 9 steatotic liver disease 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
56606	solute carrier family 2 member 9	SLC2A9	Homo sapiens (human)
7779	solute carrier family 30 member 1	SLC30A1	Homo sapiens (human)
7781	solute carrier family 30 member 3	SLC30A3	Homo sapiens (human)
64924	solute carrier family 30 member 5	SLC30A5	Homo sapiens (human)
55676	solute carrier family 30 member 6	SLC30A6	Homo sapiens (human)
1317	solute carrier family 31 member 1	SLC31A1	Homo sapiens (human)
140679	solute carrier family 32 member 1	SLC32A1	Homo sapiens (human)
9197	solute carrier family 33 member 1	SLC33A1 Aliases: AT-1 AT1 Acetyl-CoA transporter 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 Bartter disease Charcot-Marie-Tooth disease type 5 Conn's syndrome Henoch-Schoenlein purpura MASA syndrome Marfan syndrome Mast syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome SPOAN syndrome Troyer syndrome Waterhouse-Friderichsen syndrome abdominal aortic aneurysm abdominal obesity-metabolic syndrome 1 acute myocardial infarction adenocarcinoma adenoma adrenal gland cancer allergic asthma amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis anxiety disorder arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma atherosclerosis atrial fibrillation autism spectrum disorder autistic disorder bestrophinopathy brain disease brain ischemia brain stem infarction breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cardiomyopathy cardiovascular system disease cataract 1 multiple types cataract 10 multiple types cataract 11 multiple types cataract 12 multiple types cataract 13 with adult i phenotype cataract 14 multiple types cataract 15 multiple types cataract 16 multiple types cataract 17 multiple types cataract 18 cataract 19 multiple types cataract 2 multiple types cataract 20 multiple types cataract 21 multiple types cataract 22 multiple types cataract 23 cataract 24 cataract 25 cataract 26 multiple types cataract 27 cataract 29 cataract 3 multiple types cataract 30 cataract 31 multiple types cataract 32 multiple types cataract 33 cataract 34 multiple types cataract 35 cataract 37 cataract 38 cataract 39 multiple types cataract 4 multiple types cataract 40 cataract 41 cataract 42 cataract 43 cataract 44 cataract 45 cataract 46 juvenile-onset cataract 5 multiple types cataract 6 multiple types cataract 7 cataract 8 multiple types cataract 9 multiple types cataract cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease chronic kidney disease colitis colorectal cancer colorectal carcinoma congenital nystagmus congestive heart failure coronary artery disease coronary thrombosis cribriform carcinoma deafness-dystonia-optic neuronopathy syndrome dementia depressive disorder diabetes mellitus diabetic ketoacidosis dissociated nystagmus dysthymic disorder embryoma endometriosis of uterus endometriosis endomyocardial fibrosis epilepsy epithelioid leiomyosarcoma essential hypertension familial hypertrophic cardiomyopathy focal epilepsy follicular adenoma gastroenteritis generalized anxiety disorder glomerulonephritis granular cell carcinoma heart disease hepatoblastoma 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 hyperhomocysteinemia hypersensitivity vasculitis hypertension hypertensive heart disease hypertrophic cardiomyopathy ileitis ileocolitis intellectual disability intrinsic asthma kidney disease large intestine cancer learning disability leiomyosarcoma liver cancer liver cirrhosis lung benign neoplasm lung cancer lung carcinoma major depressive disorder malignant hypertension melancholic depression melanoma microcystic adenoma myocardial infarction myxoid leiomyosarcoma nephritis nephrosis neurodegenerative disease neurotic disorder nodular prostate nutmeg liver obesity obsolete melancholia obstructive sleep apnea papillary adenoma paraplegia partial motor epilepsy pathologic nystagmus periodontitis phobic disorder placental insufficiency polycystic ovary syndrome primary hyperaldosteronism progressive muscular atrophy prostate cancer prostate carcinoma prostatic adenoma pyoureter renovascular hypertension scleroderma secondary hypertension sensorineural hearing loss sensory peripheral neuropathy sick sinus syndrome silent myocardial infarction situs inversus skin melanoma spontaneous ocular nystagmus systemic scleroderma trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tuberous sclerosis tubular adenocarcinoma type 2 diabetes mellitus vesicoureteral reflux visual epilepsy
6569	solute carrier family 34 member 1	SLC34A1	Homo sapiens (human)
10568	solute carrier family 34 member 2	SLC34A2	Homo sapiens (human)

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