|
891
|
|
|
TNF superfamily member 8 |
CD153, CD30L, CD30LG, TNLG3A |
|
|
892
|
|
|
Thymocyte selection associated family member 2 |
C1orf38, ICB-1, ICB1 |
|
|
893
|
|
|
T-box transcription factor 4 |
ICPPS, PAPPAS, SPS |
17q23.1-q23.2 deletion syndrome, 17q23.1-q23.2 duplication syndrome, Atrial septal defect, Camptodactyly of fingers, Chronic obstructive pulmonary disease, Clubfoot, Congenital clubfoot, Congenital contracture, Congenital epicanthus, Short femur, Coxa magna, Coxopodopatellar syndrome, Dwarfism, Frontal bossing, Gastroesophageal reflux disease, Heritable pulmonary arterial hypertension, High palate, Microcephaly, Micrognathism, Microstomia, Otitis media, Patent ductus arteriosus, Pulmonary arterial hypertension, Pulmonary arterial hypertension associated with congenital heart disease, Pulmonary hypertension, Scoliosis, Small patella syndrome, Stiff-person syndrome, StrabismusView all (14 more) |
|
894
|
|
|
Trans-2,3-enoyl-CoA reductase |
GPSN2, MRT14, SC2, TER |
Absence of septum pellucidum, Autism, Central visual impairment, Cerebral atrophy, Cortical dysplasia, Developmental delay, Dyskinetic syndrome, Dyssomnia, Hypoplasia of corpus callosum, Mental retardation, Mental depression, Microcephaly, Motor delay, Non-syndromic intellectual disability, Polymicrogyria, Salaam seizures, Seizure, Sleep disorders, Stereotyped behaviorView all (4 more) |
|
895
|
|
|
Transmembrane protein 59 |
C1orf8, DCF1, HSPC001, PRO195, UNQ169 |
|
|
896
|
|
|
Tumor protein p53 inducible protein 3 |
PIG3 |
|
|
897
|
|
|
TCL1 family AKT coactivator B |
SYN-1, TML1 |
|
|
898
|
|
|
Translocation associated membrane protein 2 |
- |
|
|
899
|
|
|
Transmembrane protein 63A |
HLD19, KIAA0792, hTMEM63A |
|
|
900
|
|
|
TBK1 binding protein 1 |
ProSAPiP2, SINTBAD |
|
