Genesⓘ

Dataset:
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "T"
151 to 160 of 913 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

151
TBC1 domain family member 21
MgcRabGAP
Exfoliation syndrome

152
Transmembrane protein 92
-
Cerebellar atrophy, Developmental delay, Hydrocephalus

153
Transient receptor potential cation channel subfamily V member 3
FNEPPK2, OLMS, OLMS1, VRL3
Alopecia, Anhidrosis, Hearing loss, Hyperhidrosis palmaris et plantaris, Hyperkeratosis, Hypodontia, Hypotrichosis, Isolated focal non-epidermolytic palmoplantar keratoderma, Lung neoplasms, Melanoma, Mutilating palmoplantar keratoderma with periorificial keratotic plaques, Nail diseases, Nail dysplasia, Nail dystrophy, Olmsted syndrome
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154
Tubulin tyrosine ligase like 9
C20orf125
Liver neoplasms, Liver cancer, Sclerocystic ovaries, Polycystic ovary syndrome

155
Transmembrane serine protease 6
IRIDA, MT2
Anemia, Breast cancer, Hyperkeratosis, Ichthyosis, Intrahepatic cholestasis, Irida syndrome, Iron deficiency anemia, Mental retardation, Nervous system diseases

156
Tubulin tyrosine ligase like 8
-
Diabetes mellitus

157
TOG array regulator of axonemal microtubules 2
FAM179A
Narcolepsy

158
TLE family member 5, transcriptional modulator
AES, AES-1, AES-2, ESP1, GRG, GRG5, Grg-5
Myocardial ischemia

159
Tripartite motif containing 60
RNF129, RNF33
Hashimoto disease

160
Translocase of inner mitochondrial membrane 8A
DDP, DDP1, DFN1, MTS, TIM8
Agammaglobulinemia, Apraxia, Attention deficit hyperactivity disorder, Central visual impairment, Dementia, Disorder of eye, Dysarthria, Dysphagia, Jensen syndrome, Mohr-tranebjaerg syndrome, Myopia, Optic atrophy, Paranoia, Sensorineural hearing loss, Sensory neuropathy