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"
191 to 200 of 321 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

191
Bridge-like lipid transfer protein family member 3B
SHIP164, SHIP164A, UHRF1BP1L
Juvenile arthritis, Juvenile idiopathic arthritis, Oligoarticular juvenile idiopathic arthritis

192
Biliverdin reductase A
BLVR, BVR, BVRA, BVRalpha
Cataract, Cholelithiasis, Hyperbiliverdinemia, Liver cirrhosis

193
Biliverdin reductase B
BVRB, FLR, HEL-S-10, SDR43U1
Esophageal squamous cell carcinoma, Stomach neoplasms

194
Basic helix-loop-helix ARNT like 1
ARNTL, ARNTL1, BMAL1c, JAP3, MOP3, PASD3, TIC, bHLHe5
Auditory system disease, Benign prostatic hyperplasia, Bipolar disorder, Breast cancer, Cardiovascular disease, Obstructive pulmonary disease, Coronary artery disease, Bipolar depression, Major depressive disorder, Esophageal cancer, Heart failure, Hyperbilirubinemia, Hypertension, Female infertility, Irritable bowel syndrome
View all (15 more)

195
Basic helix-loop-helix ARNT like 2
ARNTL2, CLIF, MOP9, PASD9, bHLHe6
Bipolar disorder, Diabetes mellitus type 2, Hypertension

196
BMERB domain containing 1
C16orf45, MINP
Insomnia, Major depressive disorder, Metabolic syndrome, Psoriasis, Creutzfeldt-jakob disease, Testicular carcinoma, Testicular germ cell tumor, Diabetes mellitus type 2

197
Bcl2 modifying factor
-
Lymphocytic leukemia, Hodgkin lymphoma, Lymphocytic b-cell leukemia, Liver cirrhosis, Lymphoid leukemia, Multiple myeloma, Diabetes mellitus type 2

198
BMI1 proto-oncogene, polycomb ring finger
FLVI2/BMI1, PCGF4, RNF51, flvi-2/bmi-1
Glioblastoma, Glioma, Hirschsprung disease, Myeloid leukemia, Myelodysplastic syndrome, Osteosarcoma

199
Bone morphogenetic protein 1
OI13, PCOLC, PCP, PCP2, TLD
Alzheimer disease, Jeune syndrome, Bone fragility with contractures, arterial rupture, and deafness, Coronary artery disease, Major depressive disorder, Desbuquois syndrome, Interstitial lung disease, Myocardial infarction, Osteogenesis imperfecta, Osteoporosis-pseudoglioma syndrome, Pulmonary surfactant metabolism dysfunction

200
Bone morphogenetic protein 10
-
Rhinosinusitis, Congenital heart disease, Heart failure, Left ventricular disease, Pulmonary arterial hypertension