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 1165 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

531
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

532
Alkaline phosphatase, germ cell
ALPPL, ALPPL2, GCAP
Nephrotic syndrome

533
Alkaline phosphatase, intestinal
IAP
Inflammatory bowel disease, Urolithiasis

534
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

535
Alpha kinase 2
HAK
Alzheimer disease, Eczema, Multiple sclerosis, Nonalcoholic fatty liver disease, Osteoarthritis, Scoliosis

536
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

537
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
View all (7 more)

538
Alkaline phosphatase, placental
ALP, ALPI, IAP, PALP, PLAP, PLAP-1
Autism

539
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

540
ALS2 C-terminal like
RN49018
Coronary artery disease, Schizophrenia