Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "A"
211 to 220 of 912 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

211
Aristaless related homeobox
CT121, EIEE1, ISSX, MRX29, MRX32, MRX33, MRX36, MRX38, MRX43, MRX54, MRX76, MRX87, MRXS1, PRTS
Arachnoid cysts, Autism, Developmental and epileptic encephalopathy, Hydranencephaly, Intellectual developmental disorder, x-linked, Intellectual developmental disorder, Lissencephaly, x-linked, X-linked intellectual disability, Partington syndrome, Partington x-linked mental retardation syndrome, Periventricular heterotopia, Russell-silver syndrome, West syndrome, X-linked complex neurodevelopmental disorder, X-linked lissencephaly
View all (1 more)

212
ADAM metallopeptidase with thrombospondin type 1 motif 15
DA12
Distal arthrogryposis, Open angle glaucoma

213
ADAM metallopeptidase with thrombospondin type 1 motif 16
ADAMTS16s
Breast cancer, Colorectal cancer, Ovarian cancer

214
ADAM metallopeptidase with thrombospondin type 1 motif 17
WMS4
Anterior segment mesenchymal dysgenesis, Blood coagulation disorder, Carpal tunnel syndrome, Colorectal cancer, Desbuquois syndrome, Gastrointestinal neoplasm, Liver neoplasm, Osteosarcoma, Ovarian cancer, Ovarian serous carcinoma, Severe acute respiratory syndrome, Weill-marchesani syndrome

215
ADAM metallopeptidase with thrombospondin type 1 motif 18
ADAMTS21, KNO2, MMCAT
Alzheimer disease, Androgenetic alopecia, Autism, Gastric cancer, Gastrointestinal neoplasm, Insomnia, Knobloch syndrome, Leber congenital amaurosis, Metabolic syndrome, Nonalcoholic fatty liver disease, Dental caries, Retinitis pigmentosa, Diabetes mellitus, type 2

216
ADAM metallopeptidase with thrombospondin type 1 motif 19
CVDP2
Bipolar disorder, Cardiac valvular dysplasia, Congenital heart defects, Congenital hemivertebra, Heart valve disease, Heart valve prolapse, Major depressive disorder, Open angle glaucoma, Schizophrenia, Scoliosis

217
ASXL transcriptional regulator 1
BOPS, MDS
Autism, Bohring syndrome, Bohring-opitz syndrome, Myelomonocytic leukemia, Developmental delay, Global developmental delay, Gross motor development delay, Hypertrichosis, Insomnia, Intellectual developmental disorder, Promyelocytic leukemia, Myelodysplastic syndrome, Rubinstein-taybi syndrome, Intellectual disability, Systemic mastocytosis
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218
AFG3 like matrix AAA peptidase subunit 1, pseudogene
AFG3, AFG3L1

219
Afamin
ALB2, ALBA, ALF
Kidney failure, Liver cirrhosis, Prostate cancer

220
Alpha fetoprotein
AFPD, FETA, HPAFP
Breast neoplasm, Hepatocellular carcinoma, Hepatitis c, Liver cirrhosis, Liver disease, Liver neoplasm, Premature ovarian failure, Stomach neoplasms