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"
1131 to 1140 of 1185 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1131
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

1132
Tubulin gamma 2
-
Alzheimer disease, Psoriasis, Diabetes mellitus type 2

1133
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

1134
Tubulin gamma complex component 3
104p, ALP6, GCP3, Grip104, SPBC98, Spc98, Spc98p
Bipolar disorder, Cardiac embolism, Cardioembolic stroke, Cardiovascular disease, Prostate cancer

1135
Tubulin gamma complex component 4
76P, GCP-4, GCP4, Grip76, MCCRP3
Chorioretinopathy with microcephaly, Microcephaly, Optic atrophy, Retinitis pigmentosa

1136
Tubulin gamma complex component 5
GCP5
Bipolar disorder, Obsessive-compulsive disorder

1137
Tubulin gamma complex component 6
GCP-6, GCP6, MCCRP, MCCRP1, MCPHCR
Asthma, Chorioretinopathy with microcephaly, Bipolar disorder, Gastroesophageal reflux disease, Major depressive disorder, Microcephaly, Obesity, Optic atrophy, Retinitis pigmentosa

1138
Tu translation elongation factor, mitochondrial
COXPD4, EF-TuMT, EFTU, P43
Combined oxidative phosphorylation deficiency, Esophageal neoplasms, Hypogonadism, Inflammatory bowel disease, Metabolic syndrome, Mitochondrial disease, Diabetes mellitus type 2

1139
Tuftelin 1
WHSF
Myocardial infarction, Seborrheic keratosis, Woolly hair-skin fragility syndrome

1140
Taurine up-regulated 1
LINC00080, NCRNA00080, TI-227H
Alzheimer disease, Bulimia, Liver cirrhosis