|
361
|
|
|
Transmembrane protein 138 |
HSPC196 |
Arima syndrome, Autism, Cerebellar vermis agenesis, Ciliopathies, Congenital cerebral hernia, Congenital coloboma of iris, Congenital ocular coloboma, Developmental delay, Dysmorphic features, Fundus coloboma, Hirschsprung disease, Hydrocephalus, Joubert syndrome, Joubert syndrome with oculorenal defect, Kidney disease, Malformation of cortical development, Meckel-gruber syndrome, Mental retardation, Nystagmus, Occipital encephalocele, Oculomotor apraxia, Oculovestibuloauditory syndrome, Polycystic kidney disease, Polydactyly, Polydactyly of toes, Ptosis, Renal insufficiency, Retinal coloboma, Retinal dystrophy, Scoliosis, StrabismusView all (16 more) |
|
362
|
|
|
Tyrosyl-DNA phosphodiesterase 2 |
AD022, EAP2, EAPII, TTRAP, dJ30M3.3, hTDP2 |
Spinocerebellar ataxia, Brachycephaly, Cerebellar ataxia, epilepsy, mental retardation, Colonic neoplasms, Colorectal cancer, Colorectal neoplasms, Dentinogenesis imperfecta, Endometrial neoplasms, Hypersomnia, Mental retardation, Microcephaly, Neutropenia |
|
363
|
|
|
Tripartite motif containing 33 |
DDH4, ECTO, PTC7, RFG7, TF1G, TIF1G, TIF1GAMMA, TIFGAMMA |
|
|
364
|
|
|
Transmembrane BAX inhibitor motif containing 4 |
CGI-119, GAAP, LFG4, S1R, ZPRO |
|
|
365
|
|
|
Trafficking protein particle complex subunit 2L |
HSPC176, PERRB |
|
|
366
|
|
|
Tubulin alpha 8 |
CDCBM8, MACTHC2, TUBAL2 |
Agenesis of corpus callosum, Atrial fibrillation, Bipolar disorder, Colpocephaly, Developmental delay, Dysplastic corpus callosum, Hypoplasia of the optic nerve, Microcephaly, Hypotonia, Paroxysmal atrial fibrillation, Polymicrogyria, Polymicrogyria with optic nerve hypoplasia, Seizure, West syndrome |
|
367
|
|
|
Transmembrane 6 superfamily member 2 |
- |
|
|
368
|
|
|
Two pore segment channel 1 |
TPC1 |
|
|
369
|
|
|
Tripartite motif containing 34 |
IFP1, RNF21 |
|
|
370
|
|
|
TSPEAR antisense RNA 1 |
C21orf31, C21orf90, TSPEAR-AS2 |
|
