Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "A"
731 to 740 of 912 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

731
Actin alpha cardiac muscle 1
ACTC, ASD5, CMD1R, CMH11, LVNC4
Arrhythmogenic right ventricular cardiomyopathy, Arthrogryposis, Atrial septal defect, Cardiomyopathy, Dilated cardiomyopathy, Restrictive cardiomyopathy, Hypertrophic cardiomyopathy, Left ventricular disease, Left ventricular noncompaction cardiomyopathy, Stomach neoplasms, Wolff-parkinson-white syndrome

732
Actin gamma 1
ACT, ACTG, DFNA20, DFNA26, HEL-176
Isolated sensorineural deafness, Nonsyndromic hearing loss, Congenital anomalies of the kidney and urinary tract, Carcinoma, Coloboma, Congenital myopathy, Congenital ocular coloboma, Craniofacial abnormalities, Deafness, Alzheimer disease, Hearing impairment, Insomnia, Lissencephaly, Osteoporosis

733
Actin gamma 2, smooth muscle
ACT, ACTA3, ACTE, ACTL3, ACTSG, MMIHS5, VSCM, VSCM1
Bell's palsy, Intestinal vascular insufficiency, Colonic neoplasm, Intestinal obstruction, Megacystis microcolon intestinal hypoperistalsis syndrome, Visceral myopathy, Visual disorder

734
Ataxin 8
-
Spinocerebellar ataxia

735
AGBL1 antisense RNA 1
-

736
Adenosylmethionine decarboxylase 1 pseudogene 3
-

737
ALMS1 centrosome and basal body associated protein
ALSS
Alstrom syndrome, Anorexia nervosa, Attention deficit hyperactivity disorder, Bardet-biedl syndrome, Bipolar disorder, Cardiomyopathy, Cervical cancer, Kidney disease, Colorectal cancer, Cone-rod dystrophy, Desbuquois syndrome, Down syndrome, Fetal akinesia deformation sequence, Hearing impairment, Hyperopia
View all (12 more)

738
AHNAK nucleoprotein
AHNAK1, AHNAKRS, PM227
Alzheimer disease, Bone fracture, Renal cell carcinoma, Obstructive pulmonary disease, Melanoma, Hypertrophic cardiomyopathy, Liver cirrhosis

739
ALG8 alpha-1,3-glucosyltransferase
CDG1H, PCLD3
Congenital disorder of glycosylation, Polycystic kidney disease, Major depressive disorder, Polycystic liver disease

740
ASPSCR1 tether for SLC2A4, UBX domain containing
ASPCR1, ASPL, ASPS, RCC17, TUG, UBXD9, UBXN9
Attention deficit hyperactivity disorder, Insomnia, Metabolic syndrome, Willis-ekbom disease, Sarcoma, Substance abuse, Diabetes mellitus, type 2