Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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14251 to 14260 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

14251
Tubulin alpha 3c
TUBA2, bA408E5.3
Alzheimer disease, Coronary aneurysm

14252
Tubulin alpha 3d
H2-ALPHA, KTCN9, TUBA2
Keratoconus

14253
Tubulin alpha 3e
-
Neurodevelopmental disorder, Congenital microcephaly, Global developmental delay, Lissencephaly, Non-specific syndromic intellectual disability

14254
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

14255
Tubulin alpha 4b
TUBA4
Blepharoptosis

14256
Tubulin alpha 8
CDCBM8, MACTHC2, TUBAL2
Atrial fibrillation, Atrial flutter, Macrothrombocytopenia, Bipolar disorder, Duane retraction syndrome, Polymicrogyria

14257
Tubulin alpha like 3
-
Neurodevelopmental disorder, Non-specific syndromic intellectual disability, Hypertension

14258
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, Enterocolitis, Schizophrenia, Hereditary spastic paraplegia

14259
Tubulin beta 1 class VI
MACTHC1
Macrothrombocytopenia, Congenital hypothyroidism, Hemorrhagic disease, Meniere disease, Thrombocytopenia

14260
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