Genesⓘ

Dataset:
? Protein-coding genes with reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
511 to 520 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

511
ALG3 alpha-1,3- mannosyltransferase
CDG1D, CDGS4, CDGS6, D16Ertd36e, NOT56L, Not56, not
Congenital disorder of glycosylation, Desbuquois syndrome, Intellectual developmental disorder

512
ALG5 dolichyl-phosphate beta-glucosyltransferase
PKD7, bA421P11.2
Polycystic kidney disease

513
ALG6 alpha-1,3-glucosyltransferase
CDG1C
Congenital disorder of glycosylation, Cystic kidney disease

514
ALG8 alpha-1,3-glucosyltransferase
CDG1H, PCLD3
Congenital disorder of glycosylation, Polycystic kidney disease, Major depressive disorder, Polycystic liver disease

515
ALG9 alpha-1,2-mannosyltransferase
CDG1L, DIBD1, GIKANIS, LOH11CR1J
Polycystic kidney disease, Congenital disorder of glycosylation, Cardiovascular disease, Desbuquois syndrome, Gout, Hypertension, Polycystic liver disease

516
238
ALK
ALK receptor tyrosine kinase
ALK1, CD246, NBLST3
Eczema, Behcet disease, Brain infarction, Brain neoplasms, Breast neoplasm, Non-small-cell lung carcinoma, Renal cell carcinoma, Cataract, Central nervous system cancer, Conotruncal cardiac defect, Coronary artery disease, Dementia, Dental caries, Major depressive disorder, Diabetic maculopathy
View all (14 more)

517
ALK and LTK ligand 1
AUGA, AUGB, FAM150A, UNQ9433
Lung cancer

518
ALK and LTK ligand 2
AUGA, FAM150B, PRO1097, RGPG542
Willis-ekbom disease

519
AlkB homolog 1, histone H2A dioxygenase
ABH, ABH1, ALKBH, alkB, hABH
Color vision deficiency

520
AlkB homolog 3, alpha-ketoglutarate dependent dioxygenase
ABH3, DEPC-1, DEPC1, PCA1, hABH3
Astrocytoma, Metabolic syndrome, Diabetes mellitus, type 2