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 "B"
281 to 290 of 321 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

281
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)

282
BSD domain containing 1
-
Insomnia

283
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

284
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)

285
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

286
Binder of sperm protein homolog 1
BSP1, ELSPBP2
Peripheral vascular disease, Vascular disease

287
Bone marrow stromal cell antigen 1
CD157, cADPR2
Lewy body disease, Lung disease, Parkinson disease, Scoliosis

288
Brain specific homeobox
BSX1
Atrial fibrillation, Autism, Cancer, Coronary artery disease, Diabetes mellitus, Heart failure, Stroke

289
B-TFIID TATA-box binding protein associated factor 1
MOT1, TAF(II)170, TAF172, TAFII170
Attention deficit hyperactivity disorder, Scoliosis, Substance abuse, Diabetes mellitus type 2

290
BTB domain containing 1
C15orf1, NS5ATP8
Obstructive pulmonary disease, Kawasaki disease