Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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1171 to 1180 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1171
Beta-2-microglobulin
AMYLD6, IMD43, MHC1D4
Amyloidosis, Ankylosing spondylitis, Arthritis, Autoimmune disease, Beta2-microglobulinic amyloidosis, Bare lymphocyte syndrome, Esophageal squamous cell carcinoma, Visceral amyloidosis, Heart disease, Hypergammaglobulinemia, Immunodeficiency, Inflammatory bowel disease, Kidney disease, Kidney failure, Diffuse large b-cell lymphoma
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1172
Beta-1,3-N-acetylgalactosaminyltransferase 2
B3GalNAc-T2, MDDGA11
Nonsyndromic intellectual disability, Congenital muscular dystrophy due to dystroglycanopathy, Intellectual developmental disorder, Kenny-caffey syndrome, Muscle eye brain disease, Oligodendroglioma, Walker-warburg syndrome

1173
Beta-1,3-galactosyltransferase 1
beta3Gal-T1
Alzheimer disease, Color vision deficiency, Diabetic ketoacidosis, Diverticular disease, Insomnia, Neurotic disorder, Obesity, Psychiatric disorders, Diabetes mellitus type 2

1174
Beta-1,3-galactosyltransferase 2
BETA3GALT2, GLCT2, beta3Gal-T2
Hyperparathyroidism

1175
Beta-1,3-galactosyltransferase 4
BETA3GALT4, GALT2, GALT4
Inflammatory bowel disease, Rheumatoid arthritis

1176
Beta-1,3-galactosyltransferase 5
B3GalT-V, B3GalTx, B3T5, GLCT5, beta-1,3-GalTase 5, beta-3-Gx-T5, beta3Gal-T5
Asthma, Cardiac arrhythmia, Corneal astigmatism, Gout, Major depressive disorder, Psychiatric disorders, Respiratory system disease

1177
Beta-1,3-galactosyltransferase 6
ALGAZ, EDSP2, EDSSPD2, SEMDJL1, beta3GalT6
Congenital disorder of glycosylation, Bone fragility with contractures, arterial rupture, and deafness, Desbuquois syndrome, Ehlers-danlos syndrome, Larsen syndrome, Osteoporosis-pseudoglioma syndrome, Spondyloepimetaphyseal dysplasia, Spondyloepiphyseal dysplasia

1178
Beta-1,3-glucuronyltransferase 1
CD57, GLCATP, GLCUATP, HNK1, LEU7, NK-1, NK1
Insomnia, Lung cancer, Nonalcoholic fatty liver disease, Prostate cancer, Schizophrenia

1179
Beta-1,3-glucuronyltransferase 2
GLCATS
Autism, Barrett esophagus, Insomnia, Obesity, Schizophrenia, Venous thromboembolism

1180
Beta-1,3-glucuronyltransferase 3
GLCATI, JDSCD, glcUAT-I
Bone fragility with contractures, arterial rupture, and deafness, Neurodevelopmental disorder, Craniofacial abnormalities, Desbuquois syndrome, Larsen syndrome, Non-specific syndromic intellectual disability, Osteoporosis-pseudoglioma syndrome