Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "A"
641 to 650 of 912 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

641
Adaptor related protein complex 5 subunit mu 1
C14orf108, MUDENG, Mu5, MuD
Astrocytoma, Renal cell carcinoma, Central nervous system cancer, Glioma, Scoliosis

642
Acylglycerol kinase
CATC5, CTRCT38, MTDPS10, MULK
Cataract, Sengers syndrome, Kidney disease, Congenital cataract, Congenital cataract hypertrophic cardiomyopathy mitochondrial myopathy syndrome, Kidney failure, Mitochondrial disease, Mood disorder, Prion disease, Psoriasis, Trichohepatoenteric syndrome

643
AXL receptor tyrosine kinase
ARK, AXL3, JTK11, Tyro7, UFO
Non-small-cell lung carcinoma, Coronary artery disease, Diabetes mellitus type 2, Diabetic neuropathy, Hypogonadotropic hypogonadism, Hypopituitarism, Growth hormone deficiency, Kallmann syndrome, Kidney neoplasm, Liver cirrhosis, Pancreatic neoplasm, Panhypopituitarism, Pituitary dwarfism, Pituitary short stature, Sheehan syndrome

644
Adenylate cyclase 10
HCA2, HEL-S-7a, SAC, SACI, Sacy, hsAC
Hypercalciuria, Major depressive disorder, Male infertility

645
Allantoicase
ALC
Dental caries, Diabetic neuropathy, Obesity

646
Rho GTPase activating protein 15
BM046
Alzheimer disease, Androgenetic alopecia, Anxiety disorder, Asthma, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Chondromalacia, Coronary artery disease, Digestive system disease, Diverticular disease, Diverticulitis, Gallstones, Insomnia, Major depressive disorder
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647
ASH1 like histone lysine methyltransferase
ASH1, ASH1L1, KMT2H, MRD52
Atrial fibrillation, Nonsyndromic intellectual disability, Breast cancer, Gastric cancer, Global developmental delay, Gout, Intellectual developmental disorder, Lewy body disease, Liver neoplasm, Major depressive disorder, Neurodevelopmental disorders, Parkinson disease, Prostatic neoplasm

648
Apolipoprotein M
G3a, HSPC336, NG20, apo-M
Ischemic heart disease, Coronary artery disease, Diabetes mellitus type 1, Diabetes mellitus type 2, Lung cancer, Myocardial ischemia, Non-small cell lung carcinoma, Rheumatoid arthritis, Sarcoidosis, Squamous cell carcinoma, Upper aerodigestive tract neoplasm

649
ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase
CDG1K, HMAT1, HMT-1, HMT1, MT-1, Mat-1, hMat-1
Congenital disorder of glycosylation

650
ANKH inorganic pyrophosphate transport regulator
ANK, CCAL2, CMDJ, CPPDD, HANK, MANK, SLC62A1
Alzheimer disease, Calcium metabolism disorders, Chondrocalcinosis, Craniofacial abnormalities, Craniometadiaphyseal dysplasia , Craniometaphyseal dysplasia, Desbuquois syndrome, Diabetes mellitus, Diabetic neuropathy, Endometriosis, Calcium pyrophosphate deposition, Glaucoma, Intellectual developmental disorder, Open angle glaucoma, Prostate cancer
View all (4 more)