Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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1361 to 1370 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1361
Bridge-like lipid transfer protein family member 3B
SHIP164, SHIP164A, UHRF1BP1L
Juvenile arthritis, Juvenile idiopathic arthritis, Oligoarticular juvenile idiopathic arthritis

1362
Biliverdin reductase A
BLVR, BVR, BVRA, BVRalpha
Cataract, Cholelithiasis, Hyperbiliverdinemia, Liver cirrhosis

1363
Biliverdin reductase B
BVRB, FLR, HEL-S-10, SDR43U1
Esophageal squamous cell carcinoma, Stomach neoplasms

1364
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)

1365
Basic helix-loop-helix ARNT like 2
ARNTL2, CLIF, MOP9, PASD9, bHLHe6
Bipolar disorder, Diabetes mellitus type 2, Hypertension

1366
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

1367
Bcl2 modifying factor
-
Lymphocytic leukemia, Hodgkin lymphoma, Lymphocytic b-cell leukemia, Liver cirrhosis, Lymphoid leukemia, Multiple myeloma, Diabetes mellitus type 2

1368
BMI1 proto-oncogene, polycomb ring finger
FLVI2/BMI1, PCGF4, RNF51, flvi-2/bmi-1
Glioblastoma, Glioma, Hirschsprung disease, Myeloid leukemia, Myelodysplastic syndrome, Osteosarcoma

1369
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

1370
Bone morphogenetic protein 10
-
Rhinosinusitis, Congenital heart disease, Heart failure, Left ventricular disease, Pulmonary arterial hypertension