Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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1441 to 1450 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1441
Bromodomain and PHD finger containing 3
-
Autism, Colitis

1442
BR serine/threonine kinase 1
SAD-B, hSAD1
Breast cancer, Osteoarthritis

1443
BR serine/threonine kinase 2
C11orf7, PEN11B, SAD-A, SAD1, SADA, STK29
Nonsyndromic intellectual disability, Neurodevelopmental disorder, Hereditary hemolytic anemia, Intellectual developmental disorder, Metabolic syndrome, Non-specific syndromic intellectual disability, Schizophrenia, Diabetes mellitus type 2

1444
Bromodomain and WD repeat domain containing 1
C21orf107, CILD51, DCAF19, N143, WDR9, WRD9
Agammaglobulinemia, Atrial fibrillation, Atrial flutter, Attention deficit hyperactivity disorder, Autism, Bronchiectasis, Ciliary dyskinesia, Heart failure, Male infertility, Metabolic syndrome, Osteoarthritis, Premature ovarian failure, Situs inversus, Substance abuse, Diabetes mellitus type 2

1445
Bromodomain and WD repeat domain containing 3
BRODL, DCAF20, MRX93, XLID93
Autism, Developmental delay, Rolandic epilepsy, Intellectual developmental disorder, x-linked, Intellectual developmental disorder, Neurodevelopmental disorder, Non-specific syndromic intellectual disability, Partington syndrome, West syndrome, X-linked intellectual disability

1446
BSCL2 lipid droplet biogenesis associated, seipin
GNG3LG, HMN5, HMN5C, HMND13, PELD, SPG17
Asthenozoospermia, Spastic paraplegia, Berardinelli-seip congenital lipodystrophy, Charcot-marie-tooth disease, Congenital generalized lipodystrophy, Developmental and epileptic encephalopathy, Distal hereditary motor neuropathy, Distal spinal muscular atrophy, Generalized lipodystrophy, Hereditary motor and sensory neuropathies, Isolated systolic hypertension, Lipodystrophy, Mood disorder, Neonatal diabetes mellitus, Peripheral neuropathy
View all (1 more)

1447
BSD domain containing 1
-
Insomnia

1448
Basigin (Ok blood group)
5F7, CD147, EMMPRIN, EMPRIN, HAb18G, OK, TCSF
Amyotrophic lateral sclerosis, Hepatocellular carcinoma, Renal cell carcinoma, Endometriosis, Esophageal neoplasms, Alzheimer disease, Melanoma, Motor neuron disease, Pancreatic neoplasms

1449
Bassoon presynaptic cytomatrix protein
ZNF231
Alzheimer disease, Ankylosing spondylitis, Anorexia nervosa, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Obstructive pulmonary disease, Coronary artery disease, Crohn disease, Endometriosis, Epilepsy, Heart disease, Inflammatory bowel disease, Insomnia, Major depressive disorder
View all (8 more)

1450
Barttin CLCNK type accessory subunit beta
BART, DFNB73
Isolated sensorineural deafness, Bartter syndrome, Kidney disease, Coronary artery disease, Deafness, Diabetic neuropathy, Hearing impairment, Hearing loss, Myocardial infarction, Seasonal allergic rhinitis, Sensorineural deafness with renal dysfunction