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"
531 to 540 of 1170 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

531
Arachidonate 5-lipoxygenase activating protein
FLAP
Asthma, Atherosclerosis, Bipolar disorder, Brain infarction, Ischemic stroke, Cerebral palsy, Ischemic heart disease, Coronary artery disease, Crohn disease, Inflammatory bowel disease, Kidney disease, Liver disease, Myocardial infarction, Myocardial ischemia, Proteinuria
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532
Arachidonate epidermal lipoxygenase 3
ARCI3, E-LOX, LI5, eLOX-3, eLOX3
Autism, Congenital ichthyosis, Congenital ichthyosiform erythroderma, Congenital nonbullous ichthyosiform erythroderma, Ichthyosis, Lamellar ichthyosis, Prostatic neoplasms

533
Alkaline phosphatase, germ cell
ALPPL, ALPPL2, GCAP
Nephrotic syndrome

534
Alkaline phosphatase, intestinal
IAP
Inflammatory bowel disease, Urolithiasis

535
Alpha kinase 1
8430410J10Rik, LAK, ROSAH
Gouty arthritis, Atrial fibrillation, Corneal ulcer, Diabetes mellitus, Diabetic neuropathy, Eye disease, Gout, Insomnia, Nephrosclerosis, Obesity, Retinitis pigmentosa, Rheumatoid arthritis

536
Alpha kinase 2
HAK
Alzheimer disease, Eczema, Multiple sclerosis, Nonalcoholic fatty liver disease, Osteoarthritis, Scoliosis

537
Alpha kinase 3
CMH27, MAK, MIDORI
Autism, Cardiomyopathy, Cardiovascular abnormalities, Esophageal disease, Esophageal ulcer, Hypertrophic cardiomyopathy, Hypothyroidism, Left ventricular noncompaction cardiomyopathy, Mitral valve prolapse, Neurodevelopmental disorder, Schizophrenia

538
Alkaline phosphatase, biomineralization associated
AP-TNAP, APTNAP, HOPS, HPPA, HPPC, HPPI, HPPO, TNALP, TNAP, TNS-ALP, TNSALP
Hypophosphatasia, Alzheimer disease, Aortic stenosis, Aortic valve disease, Bladder calculus, Bone disease, Bone fragility with contractures, arterial rupture, and deafness, Calcinosis, Childhood hypophosphatasia, Connective tissue disease, Desbuquois syndrome, Hyperparathyroidism, Liver disease, Metabolic bone disorder, Micromelia
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539
Alkaline phosphatase, placental
ALP, ALPI, IAP, PALP, PLAP, PLAP-1
Autism

540
Alsin Rho guanine nucleotide exchange factor ALS2
ALS2CR6, ALSJ, IAHSP, PLSJ
Motor neuron disease, Amyotrophic lateral sclerosis, Global developmental delay, Hypertyrosinemia, Spastic paraplegia, Hereditary spastic paraplegia