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"
1111 to 1120 of 1188 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1111
Tweety family member 2
C17orf29
Hearing loss

1112
Tweety family member 3
-
Cerebral amyloid angiopathy, Schizophrenia

1113
TUB bipartite transcription factor
RDOB, rd5
Autism, Coronary artery disease, Essential tremor, Hearing loss, Lung cancer, Retinitis pigmentosa

1114
Tubulin alpha 1a
B-ALPHA-1, LIS3, TUBA3
Basal cell carcinoma, Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay, Cerebral palsy, Congenital fibrosis of extraocular muscles, Congenital neurologic anomalies, Cryptorchidism, Dandy-walker syndrome, Myoclonic encephalopathy, Fetal akinesia deformation sequence, Global developmental delay, Lissencephaly, Macrogyria, Cortical development malformation, Microcephaly, Movement disorder
View all (6 more)

1115
Tubulin alpha 1b
K-ALPHA-1
Congenital fibrosis of extraocular muscles, Neuromuscular disease, Osteoporosis

1116
Tubulin alpha 1c
OZEMA24, TUBA6, bcm948
Breast cancer, Cancer, Colorectal cancer, Estrogen-receptor negative breast cancer, Lung cancer, Oocyte maturation defect, Osteoporosis, Ovarian cancer, Ovarian serous carcinoma, Prostate cancer, Squamous cell carcinoma, Stomach neoplasms

1117
Tubulin alpha 3c
TUBA2, bA408E5.3
Alzheimer disease, Coronary aneurysm

1118
Tubulin alpha 3d
H2-ALPHA, KTCN9, TUBA2
Keratoconus

1119
Tubulin alpha 3e
-
Neurodevelopmental disorder, Congenital microcephaly, Global developmental delay, Lissencephaly, Non-specific syndromic intellectual disability

1120
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