Genesⓘ

Dataset:
? Protein-coding genes with reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
541 to 550 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

541
ALS2 C-terminal like
RN49018
Coronary artery disease, Schizophrenia

542
ALX homeobox 1
CART1, FND3, HEL23
Craniofacial abnormalities, Desbuquois syndrome, Frontonasal dysplasia, Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome

543
257
ALX homeobox 3
FND, FND1
Desbuquois syndrome, Frontonasal dysplasia, Neural tube defect, Neural tube defects, x-linked, Open angle glaucoma

544
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

545
Aly/REF export factor
ALY, ALY/REF, BEF, REF, THOC4
Basal cell carcinoma

546
Alpha-methylacyl-CoA racemase
AMACRD, CBAS4, P504S, RACE, RM
Alpha-methylacyl-coa racemase deficiency, Congenital bile acid synthesis defect, Colorectal neoplasm, Hereditary motor and sensory neuropathies, Hereditary sensory and motor neuropathy, Iga nephropathy, Liver cirrhosis, Liver disease, Mitochondrial complex deficiency, Prostatic neoplasm, Retinitis pigmentosa, Schizophrenia, Spastic ataxia

547
258
Ameloblastin
AI1F
Amelogenesis imperfecta, Bone fragility with contractures, arterial rupture, and deafness, Coronary artery disease, Dentin dysplasia, Dentinogenesis imperfecta, Osteoporosis-pseudoglioma syndrome

548
259
Alpha-1-microglobulin/bikunin precursor
A1M, EDC1, HCP, HI30, IATIL, ITI, ITIL, ITILC, UTI
Transitional cell carcinoma, Kidney failure, Mood disorder, Orofacial cleft

549
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

550
262
Adenosylmethionine decarboxylase 1
ADOMETDC, AMD, SAMDC
Developmental and epileptic encephalopathy, Lymphoid leukemia