Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "A"

821 to 830 of 912 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
821	84920	ALG10	ALG10 alpha-1,2-glucosyltransferase	ALG10A, DIE2, KCR1	Long qt syndrome
822	84962	AJUBA	Ajuba LIM protein	JUB	Esophagus neoplasm
823	85300	ATCAY	ATCAY kinesin light chain interacting caytaxin	BNIP-H, CLAC	Cerebellar ataxia, Cerebellar hypoplasia, Developmental delay, Dysarthria, Nystagmus
824	85365	ALG2	ALG2 alpha-1,3/1,6-mannosyltransferase	CDG1I, CDGIi, CMS14, CMSTA3, NET38, hALPG2	Cataract, Congenital coloboma of iris, Congenital disorder of glycosylation, Myasthenic syndrome, Congenital myasthenic syndromes with glycosylation defect, Congenital ocular coloboma, Developmental delay, Facial paralysis, High palate, Impaired cognition, Mental retardation, Motor delay, Myasthenia gravis, Myopathy, Nystagmus, Ptosis, Scoliosis View all (2 more)
825	8540	AGPS	Alkylglycerone phosphate synthase	ADAP-S, ADAS, ADHAPS, ADPS, ALDHPSY, RCDP3	Chondrodysplasia punctata, Short femur, Congenital lipodystrophy, Rhizomelia, Rhizomelic chondrodysplasia punctata
826	8542	APOL1	Apolipoprotein L1	APO-L, APOL, APOL-I, FSGS4	Breast cancer, Diabetic nephropathy, Genetic steroid-resistant nephrotic syndrome, Glomerular hyalinosis, Glomerulonephritis, Glomerulosclerosis, Kidney disease, Kidney failure, Nephritis, Vitamin d deficiency
827	8546	AP3B1	Adaptor related protein complex 3 subunit beta 1	ADTB3, ADTB3A, HPS, HPS2, PE	Albinism, Asthma, Developmental dysplasia of the hip, Hermansky-pudlak syndrome, Hermansky-pudlak syndrome with neutropenia, Knee osteoarthritis, Leukemia, Lung diseases, Mental retardation, Microcephaly, Motor delay, Neutropenia, Nystagmus, Ocular albinism, Periodontitis View all (3 more)
828	86	ACTL6A	Actin like 6A	ACTL6, ARPN-BETA, Arp4, BAF53A, INO80K, SMARCN1	Atrial septal defect, Developmental delay, Mental retardation, Otitis media, Syndromic mental retardation
829	8623	ASMTL	Acetylserotonin O-methyltransferase like	ASMTLX, ASMTLY, ASTML	Leukemia, Myeloid leukemia
830	8639	AOC3	Amine oxidase copper containing 3	HPAO, SSAO, VAP-1, VAP1	Diabetes mellitus, Diabetic nephropathy, Glomerulosclerosis, Hypertension, Kidney disease, Paratuberculosis, Renal insufficiency

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