|
181
|
|
|
Trafficking protein particle complex subunit 8 |
GSG1, HsT2706, KIAA1012, TRS85 |
|
|
182
|
|
|
Trafficking kinesin protein 1 |
DEE68, EIEE68, MILT1, OIP106 |
Attention deficit hyperactivity disorder, Autism, Cerebral atrophy, Cerebral cortical atrophy, Developmental delay, Developmental regression, Dwarfism, Dyskinetic syndrome, Epileptic encephalopathy, Gastroesophageal reflux disease, Hypodontia, Leukemia, Mental retardation, Microcephaly, Movement disorders, Non-specifi epileptic encephalopathy, Nystagmus, Optic atrophy, Ptosis, Schizophrenia, Status epilepticusView all (6 more) |
|
183
|
|
|
Tripartite motif containing 32 |
BBS11, HT2A, LGMD2H, LGMDR8, TATIP |
Bardet-biedl syndrome, Ciliopathies, Hypoplasia of the ovary, Congenital hypoplasia of penis, Cryptorchidism, Disorder of eye, Dwarfism, Facial paralysis, Hypertension, Hypogonadism, Limb-girdle muscular dystrophy, Sarcotubular myopathy, Liver fibrosis, Mental retardation, Multicystic renal dysplasia, Muscular dystrophy, Myopathy, Nephrotic syndrome, Nystagmus, Obesity, Pelvic girdle muscle atrophy, Polydactyly, Retinal diseases, Retinitis pigmentosa, Speech disorders, Syndactyly of fingers, Postaxial hand polydactylyView all (12 more) |
|
184
|
|
|
TPX2 microtubule nucleation factor |
C20orf1, C20orf2, DIL-2, DIL2, FLS353, GD:C20orf1, HCA519, HCTP4, REPP86, p100 |
|
|
185
|
|
|
TCF25 ribosome quality control complex subunit |
FKSG26, Hulp1, NULP1, PRO2620, hKIAA1049 |
|
|
186
|
|
|
Tetratricopeptide repeat domain 39A |
C1orf34, DEME-6 |
|
|
187
|
|
|
TRAF2 and NCK interacting kinase |
MRT54 |
Absence of septum pellucidum, Arsenic encephalopathy, Arthritis, Autism, Central visual impairment, Cerebral atrophy, Cortical dysplasia, Dermatologic disorders, Developmental delay, Dyskinetic syndrome, Dyssomnia, Frontotemporal dementia, Hypoplasia of corpus callosum, Mental retardation, Juvenile arthritis, Mental depression, Microcephaly, Motor delay, Non-syndromic intellectual disability, Seronegative polyarthritis, Polyarthritis, rheumatoid factor positive, Polymicrogyria, Salaam seizures, Schizophrenia, Seizure, Sleep disorders, Stereotyped behavior, Still disease, Vascular diseasesView all (14 more) |
|
188
|
|
|
TBC1 domain family member 9B |
GRAMD9B |
|
|
189
|
|
|
Tubulin tyrosine ligase like 5 |
CORD19, KIAA0998, STAMP |
Arthritis, Carpal tunnel syndrome, Cone-rod dystrophy, Juvenile arthritis, Leukemia, Nyctalopia, Seronegative polyarthritis, Polyarthritis, rheumatoid factor positive, Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome, Retinal dystrophy, Retinitis pigmentosa, Still disease |
|
190
|
|
|
TBC1 domain family member 2B |
NEDSGO |
|
