41
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Beta-1,4-galactosyltransferase 4 |
B4Gal-T4, beta4Gal-T4 |
Curated: Pancreatic cancer, Prostatic neoplasms
Unreviewed: Breast neoplasm, Colorectal neoplasm, Prostate cancer, Prostatic Neoplasms, Renal cell carcinoma
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42
|
|
|
B4GALT4 antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
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43
|
|
|
Beta-1,4-galactosyltransferase 5 |
B4Gal-T5, BETA4-GALT-IV, beta4Gal-T5, beta4GalT-V, gt-V |
Curated: Juvenile arthritis, Juvenile idiopathic arthritis, Oligoarticular juvenile idiopathic arthritis
Unreviewed: Arthritis, Astrocytoma, Breast neoplasm, Cardiomegaly, Colorectal Cancer, Diabetes, Diabetes Mellitus, Glioma, Hepatocellular carcinoma, Hypertrophy, Malignant Neoplasm, Neoplasms, Obesity, Ovarian neoplasm, Polyarthritis, Rheumatoid Factor Positive, Seronegative polyarthritis, Still Disease, Testicular disease, Uterine neoplasm
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44
|
|
|
Beta-1,4-galactosyltransferase 6 |
B4Gal-T6, beta4Gal-T6 |
Curated: Amyotrophic lateral sclerosis
Unreviewed: Colorectal Cancer, Developmental disability, Multiple Sclerosis, Schizophrenia, Skin abnormalities
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45
|
|
|
Beta-1,4-galactosyltransferase 7 |
EDSP1, EDSSLA, EDSSPD1, XGALT1, XGPT, XGPT1 |
Curated: Bone fragility with contractures, arterial rupture, and deafness, Craniofacial abnormalities, Desbuquois syndrome, Ehlers-danlos syndrome, Larsen syndrome, Osteoporosis-pseudoglioma syndrome, ehlers-danlos syndrome, spondylodysplastic type, 1
Unreviewed: Acquired Kyphoscoliosis, Aortic Valve Sclerosis, Arachnodactyly, Arthritis, Cockayne Syndrome, Colitis, Congenital disorder of glycosylation, Congenital Epicanthus, Congenital kyphoscoliosis, Congenital ocular coloboma, Congenital Pectus Carinatum, Connective Tissue Disease, Cryptorchidism, Cutis Laxa, Developmental Delay, Developmental disability, Dwarfism, Ehlers-Danlos Syndrome, Gingivitis, Glioblastoma, Glomerulonephritis, Growth disorder, Hepatocellular carcinoma, LARSEN SYNDROME, Lipodystrophy, Liver carcinoma, Macrocephaly, Microstomia, Osteochondrodysplasia, Osteopenia, Proptosis, Pulmonary Stenosis, Radioulnar Synostosis, Rheumatoid arthritis, Short clavicles, Skeletal Dysplasia, Skin abnormalities, Spermatic Cord Torsion, Spondylodysplastic Ehlers-Danlos Syndrome, Trichohepatoenteric Syndrome
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46
|
|
|
Beta-1,4-glucuronyltransferase 1 |
B3GN-T1, B3GNT1, B3GNT6, BETA3GNTI, MDDGA13, iGAT, iGNT |
Curated: Breast neoplasms, Muscle eye brain disease, Walker-warburg syndrome, muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A13
Unreviewed: Absence Of Septum Pellucidum, Agenesis Of Corpus Callosum, alpha-Dystroglycanopathy, Anencephaly, Breast Cancer, Breast Carcinoma, Cataract, Cerebellar Hypoplasia, Ciliopathies, Cobblestone Lissencephaly, Congenital Coloboma Of Iris, Congenital Hypoplasia Of Penis, Congenital Muscular Dystrophy-Dystroglycanopathy With Brain And Eye Anomalies, Cortical Dysplasia, Cryptorchidism, Dandy-Walker Syndrome, Developmental Delay, Fukuyama Type Congenital Muscular Dystrophy, Glaucoma, Hydrocephalus, Hydronephrosis, Limb-girdle muscular dystrophy, Macrocephaly, Mammary Neoplasms, Marfan Syndrome, Mental retardation, Microcephaly, Microcornea, Microphthalmos, Muscle Eye Brain Disease, Muscular dystrophy, Muscular Dystrophy-Dystroglycanopathy, Neuronal Heterotopia, Occipital Encephalocele, Optic Atrophy, Pachygyria, Penis Agenesis, Polymicrogyria, Posteriorly Rotated Ear, Retinal Detachment, Retinal Dysplasia, Retinal Dystrophy, Specific Learning Disorder, Submucosal cleft palate, Syndromic microphthalmia, Walker-Warburg Congenital Muscular Dystrophy, Walker-Warburg Syndrome
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47
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|
|
B4GAT1 divergent transcript |
- |
Curated: N/A
Unreviewed: N/A
|
48
|
|
|
- |
- |
Curated: N/A
Unreviewed: N/A
|
49
|
|
|
B9 domain containing 1 |
B9, EPPB9, JBTS27, MKS9, MKSR-1, MKSR1 |
Curated: Ciliopathy, Congenital cystic kidney disease, Aplasia of the vermis, Gastrointestinal stromal tumor, Joubert syndrome, Jeune thoracic dystrophy, Meckel-gruber syndrome, Schizophrenia
Unreviewed: Agenesis Of Corpus Callosum, Ambiguous Genitalia, Anencephaly, Aplasia Cutis Congenita, Asplenia, Cataract, Cerebellar vermis agenesis, Ciliopathies, Congenital Cerebral Hernia, Congenital Clubfoot, Congenital Coloboma Of Iris, Congenital Hepatic Fibrosis, Cryptorchidism, Cystic liver disease, Dandy-Walker Syndrome, Developmental Delay, Double Ureter, Fibrosis Of Pancreas, Foot Polydactyly, Hirschsprung Disease, Hydrocephalus, Joubert Syndrome, Liver Cancer, Liver neoplasms, Lobar Holoprosencephaly, Male Pseudohermaphroditism, Meckel Syndrome, Meckel-Gruber Syndrome, Mental retardation, Microcephaly, Microcornea, Micrognathism, Microphthalmos, Multicystic renal dysplasia, Neoplasms, Nystagmus, Occipital Encephalocele, Oculomotor apraxia, Oculovestibuloauditory Syndrome, Optic Atrophy, Oral cleft, Pancreatic Cyst, Polycystic liver disease, Polydactyly, Polydactyly Of Toes, Polymicrogyria, Postaxial hand polydactyly, Ptosis, Renal glycosuria, Sclerocornea, Scoliosis, Situs Inversus, Strabismus, Syndromic microphthalmia, Talipes, True Hermaphroditism, Urethral atresia
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50
|
|
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B9 domain containing 2 |
ICIS-1, JBTS34, MKS10, MKSR-2, MKSR2 |
Curated: 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
Unreviewed: Anencephaly, Asplenia, Cataract, Cerebellar vermis agenesis, Ciliopathies, Colorectal Cancer, Congenital Cerebral Hernia, Congenital Epicanthus, Congenital Hepatic Fibrosis, Cryptorchidism, Cystic liver disease, Dandy-Walker Syndrome, Double Ureter, Fibrosis Of Pancreas, Foot Polydactyly, Frontal bossing, Hydrocephalus, Hypospadias, Lobar Holoprosencephaly, Male Pseudohermaphroditism, Meckel Syndrome, Meckel-Gruber Syndrome, Microcephaly, Microcornea, Micrognathism, Microphthalmos, Multicystic renal dysplasia, Occipital Encephalocele, Optic Atrophy, Pancreatic Cyst, Penis Agenesis, Polycystic liver disease, Polydactyly, Postaxial hand polydactyly, Ptosis, Renal cyst, Sclerocornea, Situs Inversus, Syndromic microphthalmia, Talipes, True Hermaphroditism, Urethral atresia
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