Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "B"
191 to 200 of 258 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

191
Basigin (Ok blood group)
5F7, CD147, EMMPRIN, EMPRIN, HAb18G, OK, TCSF
Amyotrophic lateral sclerosis, Hepatocellular carcinoma, Renal cell carcinoma, Endometriosis, Esophageal neoplasm, Alzheimer disease, Melanoma, Motor neuron disease, Pancreatic neoplasm

192
Bone marrow stromal cell antigen 1
CD157, cADPR2
Lewy body disease, Lung disease, Parkinson disease, Scoliosis

193
Betacellulin
-
Androgenetic alopecia, Bronchopneumonia, Obstructive pulmonary disease, Clonal hematopoiesis, Colorectal cancer, Diabetes mellitus type 1, Diabetes mellitus type 2, Diverticular disease, Hemorrhoid, Nephrotic syndrome, Osteosarcoma, Erythropoietic protoporphyria, Psychiatric disorders, Schizophrenia

194
Biotinidase
-
Eczema, Autism, Biotinidase deficiency, Coronary artery disease, Cryptorchidism, Diverticular disease, Global developmental delay, Inflammatory skin disease, Intellectual developmental disorder, Leigh syndrome, Metabolic syndrome, Psoriasis, Diabetes mellitus, type 2

195
BTG anti-proliferation factor 1
APRO2
Juvenile arthritis, Juvenile idiopathic arthritis, Multiple myeloma, Oligoarticular juvenile idiopathic arthritis, Schizophrenia

196
Bruton tyrosine kinase
AGMX1, AT, ATK, BPK, IGHD3, IMD1, PSCTK1, XLA
Bruton type agammaglobulinemia, Common variable immunodeficiency, Desbuquois syndrome, Hypogonadotropic hypogonadism, Hypopituitarism, Growth hormone deficiency, Kallmann syndrome, Panhypopituitarism, Pituitary dwarfism, Pituitary short stature, Sheehan syndrome, X-linked agammaglobulinemia, X-linked agammaglobulinemia with growth hormone deficiency, X-linked hypogammaglobulinemia

197
BUB1 mitotic checkpoint serine/threonine kinase
BUB1A, BUB1L, MCPH30, hBUB1
Hepatocellular carcinoma, Colorectal cancer, Colorectal neoplasm, Microcephaly, Mosaic variegated aneuploidy, Prostate cancer

198
BUB1 mitotic checkpoint serine/threonine kinase B
BUB1beta, BUBR1, Bub1A, MAD3L, MVA1, SSK1, hBUBR1
Hepatocellular carcinoma, Cerebral palsy, Lymphocytic leukemia, Colorectal cancer, Colorectal neoplasm, Esophageal squamous cell carcinoma, Growth disorder, Microcephaly, Mosaic variegated aneuploidy, Rhabdomyosarcoma

199
Basic helix-loop-helix family member a9
BHLHF42, CCSPD
Camptosynpolydactyly, complex, Desbuquois syndrome, Gollop-wolfgang complex, Split hand-foot malformation, Syndactyly

200
Bestrophin 1
ARB, BEST, BMD, Best1V1Delta2, RP50, TU15B, VMD2
Distal myopathy, Vitreoretinochoroidopathy, Bestrophinopathy, Iron overload, Macular degeneration, Macular dystrophy, Nanophthalmos, Neurodegeneration with brain iron accumulation, Retinal cone dystrophy, Retinitis pigmentosa, Stargardt disease, Vitelliform macular dystrophy