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"
21 to 30 of 321 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

21
Beta-1,4-N-acetyl-galactosaminyltransferase 4
-
Hypothyroidism, Major depressive disorder, Osteoarthritis, Diabetes mellitus type 2

22
Beta-1,4-galactosyltransferase 1
B4GAL-T1, CDG2D, CLDLFIB, GGTB2, GT1, GTB, beta4Gal-T1
Congenital disorder of glycosylation, Combined low ldl and fibrinogen, Gout

23
Beta-1,4-galactosyltransferase 3
beta4Gal-T3
Variegate porphyria

24
Beta-1,4-galactosyltransferase 4
B4Gal-T4, beta4Gal-T4
Pancreatic cancer, Prostatic neoplasms

25
Beta-1,4-galactosyltransferase 5
B4Gal-T5, BETA4-GALT-IV, beta4Gal-T5, beta4GalT-V, gt-V
Juvenile arthritis, Juvenile idiopathic arthritis, Liver cirrhosis, Oligoarticular juvenile idiopathic arthritis

26
Beta-1,4-galactosyltransferase 6
B4Gal-T6, beta4Gal-T6
Amyotrophic lateral sclerosis

27
Beta-1,4-galactosyltransferase 7
EDSP1, EDSSLA, EDSSPD1, XGALT1, XGPT, XGPT1
Bone fragility with contractures, arterial rupture, and deafness, Craniofacial abnormalities, Desbuquois syndrome, Ehlers-danlos syndrome, Larsen syndrome, Osteoporosis-pseudoglioma syndrome

28
Beta-1,4-glucuronyltransferase 1
B3GN-T1, B3GNT1, B3GNT6, BETA3GNTI, MDDGA13, iGAT, iGNT
Breast neoplasms, Muscle eye brain disease, Walker-warburg syndrome

29
B9 domain containing 1
B9, EPPB9, JBTS27, MKS9, MKSR-1, MKSR1
Ciliopathy, Congenital cystic kidney disease, Aplasia of the vermis, Gastrointestinal stromal tumor, Joubert syndrome, Jeune thoracic dystrophy, Liver cirrhosis, Meckel-gruber syndrome, Schizophrenia

30
B9 domain containing 2
ICIS-1, JBTS34, MKS10, MKSR-2, MKSR2
Ciliopathy, Congenital brain malformation, Congenital hypoplasia of part of brain, Coronary artery disease, Aplasia of the vermis, Hydranencephaly, Joubert syndrome, Lissencephaly, Macrogyria, Meckel-gruber syndrome, Microgyria, Migraine, Myocardial infarction