Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "A"
471 to 480 of 1165 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

471
AKT serine/threonine kinase 2
HIHGHH, PKBB, PKBBETA, PRKBB, RAC-BETA
Lipodystrophy, Bipolar disorder, Breast neoplasms, Diabetes mellitus type 2, Partial lipodystrophy, Hypoglycemia, Nasopharyngeal carcinoma, Prostatic neoplasms

472
AKT serine/threonine kinase 3
MPPH, MPPH2, PKB-GAMMA, PKBG, PRKBG, RAC-PK-gamma, RAC-gamma, STK-2
Anorexia nervosa, Attention deficit hyperactivity disorder, Bardet-biedl syndrome, Central nervous system cancer, Glioblastoma, Glioma, Global developmental delay, Hemimegalencephaly, Insomnia, Cortical development malformation, Metabolic syndrome, Microcephaly, Myocardial infarction, Polymicrogyria, Post-traumatic stress disorder
View all (4 more)

473
AKT interacting protein
FT1, FTS
Attention deficit hyperactivity disorder, Autism, Barrett esophagus, Color vision deficiency, Esophageal disease, Gastroesophageal reflux disease, Metabolic syndrome, Rheumatic disease, Diabetes mellitus type 2

474
Aminolevulinate dehydratase
ALADH, PBGS
Sickle cell anemia, Autism, Renal cell carcinoma, Genetic predisposition to disease, Hematologic disease, Hypertension, Kidney disease, Liver cirrhosis, Liver disease, Meningioma, Porphyria cutanea tarda, Porphyria, Prostatic neoplasms, Seizures

475
5'-aminolevulinate synthase 1
ALAS, ALAS-H, ALAS3, ALASH, MIG4
Bipolar disorder, Crohn disease, Porphyria, Major depressive disorder, Neurotic disorder

476
5'-aminolevulinate synthase 2
ALAS-E, ALASE, ANH1, ASB, SIDBA1, XLDPP, XLEPP, XLSA
Sideroblastic anemia, Erythropoietic protoporphyria, Hemochromatosis, Insomnia, Porphyria, X-linked erythropoietic protoporphyria, X-linked sideroblastic anemia

477
Albumin
FDAHT, HSA, PRO0883, PRO0903, PRO1341
Analbuminemia, Angioedema, Anuria, Azoospermia, Biliary cirrhosis, Blood protein disorder, Brain disease, Brain injuries, Brain ischemia, Cardiovascular disease, Cerebrovascular disorder, Cholelithiasis, Ulcerative colitis, Congenital analbuminemia, Congestive heart failure
View all (37 more)

478
Activated leukocyte cell adhesion molecule
CD166, MEMD
Alzheimer disease, Attention deficit hyperactivity disorder, Breast cancer, Carcinoma, Basal cell carcinoma, Coronary artery disease, Erectile dysfunction, Major depressive disorder, Metabolic syndrome, Oligodendroglioma, Open angle glaucoma, Parkinson disease, Willis-ekbom disease, Schizophrenia, Scoliosis
View all (5 more)

479
Aldehyde dehydrogenase 16 family member A1
-
Gouty arthritis, Central nervous system cancer, Glioblastoma, Glioma, Gout, Hyperuricemia

480
Aldehyde dehydrogenase 18 family member A1
ADCL3, ARCL3A, GSAS, P5CS, PYCS, SPG9, SPG9A, SPG9B
De barsy syndrome, Complex spastic paraplegia, Cutis laxa, Spastic paraplegia, Accessory skin tag, Congenital neurologic anomalies, Benign pemphigus, Intellectual developmental disorder, Darier disease, Rothmund-thomson syndrome, Hereditary spastic paraplegia, Spondyloepiphyseal dysplasia