Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "T"
181 to 190 of 913 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

181
Trafficking protein particle complex subunit 8
GSG1, HsT2706, KIAA1012, TRS85
Major depressive disorder

182
Trafficking kinesin protein 1
DEE68, EIEE68, MILT1, OIP106
Attention deficit hyperactivity disorder, Autism, Developmental and epileptic encephalopathy, Developmental disability, Heart failure, Major depressive disorder, Metabolic syndrome, Sarcoidosis, Schizophrenia, Diabetes mellitus, type 2

183
Tripartite motif containing 32
BBS11, HT2A, LGMD2H, LGMDR8, TATIP
Limb girdle muscular dystrophy, Bardet-biedl syndrome, Limb-girdle muscular dystrophy, Muscular dystrophy, Myopathy, Retinitis pigmentosa, Sarcotubular myopathy

184
TPX2 microtubule nucleation factor
C20orf1, C20orf2, DIL-2, DIL2, FLS353, GD:C20orf1, HCA519, HCTP4, REPP86, p100
Hepatocellular carcinoma, Tourette syndrome, Hypertension, Myeloproliferative disorder

185
TCF25 ribosome quality control complex subunit
FKSG26, Hulp1, NULP1, PRO2620, hKIAA1049
Alzheimer disease, Basal cell carcinoma, Breast cancer

186
Tetratricopeptide repeat domain 39A
C1orf34, DEME-6
Heart failure, Liver neoplasm, Wolff-parkinson-white syndrome

187
TRAF2 and NCK interacting kinase
MRT54
Juvenile arthritis, Nonsyndromic intellectual disability, Dermatologic disorder, Dyshidrosis, Frontotemporal dementia, Intellectual developmental disorder, Juvenile idiopathic arthritis, Metabolic syndrome, Ovarian cancer, Oligoarticular juvenile idiopathic arthritis, Peripheral arterial disease, Schizophrenia, Scoliosis, Skin disease, Hypertension
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188
TBC1 domain family member 9B
GRAMD9B

189
Tubulin tyrosine ligase like 5
CORD19, KIAA0998, STAMP
Juvenile arthritis, Carpal tunnel syndrome, Central areolar choroidal dystrophy, Central nervous system cancer, Cone-rod dystrophy, Glioblastoma, Glioma, Juvenile idiopathic arthritis, Large artery stroke, Open angle glaucoma, Optic atrophy, Oligoarticular juvenile idiopathic arthritis, Retinitis pigmentosa

190
TBC1 domain family member 2B
NEDSGO
Neurodevelopmental disorder, Psychiatric disorders