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 "T"
1121 to 1130 of 1185 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1121
Tubulin beta class I
CDCBM6, CSCSC1, M40, OK/SW-cl.56, TUBB1, TUBB5
Autism, Dilated cardiomyopathy, Cervical cancer, Complex cortical dysplasia with other brain malformations, Congenital fibrosis of extraocular muscles, Congestive heart failure, Cortical dysplasia with other brain malformations, Female infertility, Heart failure, Lissencephaly, Schizophrenia, Hereditary spastic paraplegia

1122
Tubulin beta 1 class VI
MACTHC1
Macrothrombocytopenia, Congenital hypothyroidism, Hemorrhagic disease, Meniere disease, Thrombocytopenia

1123
Tubulin beta 2A class IIa
CDCBM5, TUBB, TUBB2
Juvenile arthritis, Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay, Complex cortical dysplasia with other brain malformations, Cortical dysplasia with other brain malformations, Creutzfeldt-jakob disease, Vascular dementia, Developmental disability, Juvenile idiopathic arthritis, Myeloid leukemia, Neurodevelopmental disorder, Oligoarticular juvenile idiopathic arthritis, Tubulinopathy

1124
Tubulin beta 2B class IIb
CDCBM7, PMGYSA, bA506K6.1
Carcinoma, Cerebellar ataxia, intellectual disability, and dysequilibrium, Complex cortical dysplasia with other brain malformations, Congenital fibrosis of extraocular muscles, Cortical dysplasia with other brain malformations, Dysequilibrium syndrome, Lissencephaly, Cortical development malformation, Perisylvian syndrome, Polymicrogyria, Tubulinopathy

1125
Tubulin beta 3 class III
CDCBM, CDCBM1, CFEOM3, CFEOM3A, FEOM3, TUBB4, beta-4
Autism, Basal cell carcinoma, Breast neoplasms, Complex cortical dysplasia with other brain malformations, Congenital brain malformation, Congenital fibrosis of extraocular muscles, Congenital hypoplasia of part of brain, Cortical dysgenesis with pontocerebellar hypoplasia, Cortical dysplasia with other brain malformations, Developmental disability, Hydranencephaly, Lissencephaly, Macrogyria, Male infertility single gene azoospermia, Martsolf syndrome
View all (7 more)

1126
Tubulin beta 4A class IVa
DYT4, TUBB4, beta-5
Cerebellar atrophy, Auditory neuropathy, Brown tendon sheath syndrome, Cerebral palsy, Congenital neurologic anomalies, Dystonia, Dystonia musculorum deformans, Frontotemporal dementia, Genetic torsion dystonia, Global developmental delay, Hypomyelinating leukodystrophy, Torsion dystonia, Whispering dysphonia

1127
Tubulin beta 4B class IVb
Beta2, LCAEOD, TUBB2, TUBB2C
Leber congenital amaurosis, Retinitis pigmentosa

1128
Tubulin beta 6 class V
FPVEPD, HsT1601, TUBB-5
Blepharoptosis, Facial nerve disorder, Optic atrophy, Spastic ataxia, Spinocerebellar ataxia

1129
Tubulin beta 8 class VIII
OOMD, OOMD2, OZEMA2, bA631M21.2
Female infertility, Oocyte maturation defect

1130
Tubulin delta 1
TUBD
Crohn disease, Gout, Inflammatory bowel disease, Metabolic syndrome, Polydactyly, Diabetes mellitus type 2, Ulcerative colitis