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"
541 to 550 of 1165 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

541
ALX homeobox 1
CART1, FND3, HEL23
Craniofacial abnormalities, Desbuquois syndrome, Frontonasal dysplasia, Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome

542
ALX homeobox 3
FND, FND1
Desbuquois syndrome, Frontonasal dysplasia, Neural tube defect, Neural tube defects, x-linked, Open angle glaucoma

543
ALX homeobox 4
CRS5, FND2
Androgenetic alopecia, Breast cancer, 11p11.2 deletion syndrome, Craniofacial abnormalities, Craniosynostosis, Desbuquois syndrome, Frontonasal dysplasia, Frontonasal dysplasia with alopecia and genital anomaly, Gout, Lung neoplasms, Parietal foramina, Polydactyly, Potocki-shaffer syndrome

544
Aly/REF export factor
ALY, ALY/REF, BEF, REF, THOC4
Basal cell carcinoma

545
Alpha-methylacyl-CoA racemase
AMACRD, CBAS4, P504S, RACE, RM
Alpha-methylacyl-coa racemase deficiency, Congenital bile acid synthesis defect, Colorectal neoplasms, Hereditary motor and sensory neuropathies, Hereditary sensory and motor neuropathy, Iga nephropathy, Liver disease, Mitochondrial complex deficiency, Prostatic neoplasms, Retinitis pigmentosa, Schizophrenia, Spastic ataxia

546
Ameloblastin
AI1F
Amelogenesis imperfecta, Bone fragility with contractures, arterial rupture, and deafness, Coronary artery disease, Dentin dysplasia, Dentinogenesis imperfecta, Osteoporosis-pseudoglioma syndrome

547
Alpha-1-microglobulin/bikunin precursor
A1M, EDC1, HCP, HI30, IATIL, ITI, ITIL, ITILC, UTI
Transitional cell carcinoma, Kidney failure, Mood disorder, Orofacial cleft

548
Autophagy and beclin 1 regulator 1
DCAF3, WDR94
Anorexia nervosa, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Esophageal atresia, Hypertension, Hypertrophic cardiomyopathy, Major depressive disorder, Migraine, Neural tube defect, Obsessive-compulsive disorder, Ocular sarcoidosis, Schizophrenia, Tourette syndrome, Venous thromboembolism

549
Adenosylmethionine decarboxylase 1
ADOMETDC, AMD, SAMDC
Developmental and epileptic encephalopathy, Lymphoid leukemia

550
Amidohydrolase domain containing 2
CGI-14
Childhood-onset epilepsy syndrome