Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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14261 to 14270 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

14261
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

14262
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
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14263
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

14264
Tubulin beta 4B class IVb
Beta2, LCAEOD, TUBB2, TUBB2C
Leber congenital amaurosis, Retinitis pigmentosa

14265
Tubulin beta 6 class V
FPVEPD, HsT1601, TUBB-5
Blepharoptosis, Facial nerve disorder, Liver cirrhosis, Optic atrophy, Spastic ataxia, Spinocerebellar ataxia

14266
Tubulin beta 8 class VIII
OOMD, OOMD2, OZEMA2, bA631M21.2
Female infertility, Oocyte maturation defect

14267
Tubulin delta 1
TUBD
Crohn disease, Gout, Inflammatory bowel disease, Metabolic syndrome, Polydactyly, Diabetes mellitus type 2, Ulcerative colitis

14268
Tubulin gamma 1
CDCBM4, GCP-1, TUBG, TUBGCP1
15q11.2 microdeletion syndrome, Complex cortical dysplasia with other brain malformations, Cortical dysplasia with other brain malformations, Lissencephaly, Cortical development malformation, Microcephaly, Myopathy, Myositis, Diabetes mellitus type 2

14269
Tubulin gamma 2
-
Alzheimer disease, Psoriasis, Diabetes mellitus type 2

14270
Tubulin gamma complex component 2
ALP4, GCP-2, GCP2, Grip103, PAMDDFS, SPBC97, SPC97, Spc97p, h103p, hGCP2, hSpc97
Cortical dysplasia with other brain malformations, Lissencephaly, Cortical development malformation