Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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14191 to 14200 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

14191
Tubulin alpha 4a
ALS22, CMYO26, FTDALS9, H2-ALPHA, OZEMA23, SPAX11, TUBA1
Amyotrophic lateral sclerosis, Macrothrombocytopenia, Blepharoptosis, Congenital myopathy, Frontotemporal dementia with or without amyotrophic lateral sclerosis, Oocyte maturation defect, Spastic ataxia, Diabetes mellitus type 2

14192
Tubulin alpha 4b
TUBA4
Blepharoptosis

14193
Tubulin alpha 8
CDCBM8, MACTHC2, TUBAL2
Atrial fibrillation, Atrial flutter, Macrothrombocytopenia, Bipolar disorder, Duane retraction syndrome, Polymicrogyria

14194
Tubulin alpha like 3
-
Neurodevelopmental disorder, Non-specific syndromic intellectual disability, Hypertension

14195
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

14196
Tubulin beta 1 class VI
MACTHC1
Macrothrombocytopenia, Congenital hypothyroidism, Hemorrhagic disease, Meniere disease, Thrombocytopenia

14197
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

14198
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

14199
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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14200
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