Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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1231 to 1240 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1231
Bromodomain adjacent to zinc finger domain 1A
ACF1, WALp1, WCRF180, hACF1
Hypothyroidism, Lung cancer, Non-small cell lung carcinoma, Oligodendroglioma

1232
Bromodomain adjacent to zinc finger domain 1B
WBSCR10, WBSCR9, WSTF
Alzheimer disease, Atrial fibrillation, Autism, Cancer, Coronary artery disease, Diabetes mellitus, Gout, Heart failure, Hypertriglyceridemia, Hyperuricemia, Metabolic syndrome, Migraine, Stroke, Diabetes mellitus type 2, Williams syndrome

1233
Bromodomain adjacent to zinc finger domain 2A
TIP5, WALp3
Prostatic neoplasms

1234
Bromodomain adjacent to zinc finger domain 2B
WALp4
Neurodevelopmental disorder, Hypothyroidism, Insomnia, Non-specific syndromic intellectual disability, Willis-ekbom disease

1235
BCL2 binding component 3
JFY-1, JFY1, PUMA
Alzheimer disease, Brain ischemia, Burkitt lymphoma, Esophageal neoplasms

1236
BBSome interacting protein 1
BBIP10, BBS18, NCRNA00081, bA348N5.3
Bardet-biedl syndrome, Hypogonadotropic hypogonadism, Micropenis, Obesity, Retinitis pigmentosa, Rod-cone dystrophy, Specific learning disability, Systemic lupus erythematosus, Diabetes mellitus type 2, Postaxial polydactyly

1237
Basal body orientation factor 1
C14orf45, CCDC176, FBB10
Polycystic ovary syndrome

1238
Gamma-butyrobetaine hydroxylase 1
BBH, BBOX, G-BBH, gamma-BBH
Breast cancer, Otosclerosis

1239
Bardet-Biedl syndrome 1
BBS2L2
Bardet-biedl syndrome, Ciliopathy, Insomnia, Retinitis pigmentosa, Usher syndrome

1240
Bardet-Biedl syndrome 10
C12orf58
Bardet-biedl syndrome, Ciliopathy, Intellectual developmental disorder, Macular degeneration, Optic atrophy, Polydactyly, Retinitis pigmentosa, Saldino-noonan syndrome, Postaxial polydactyly