|
251
|
|
|
TOX high mobility group box family member 3 |
CAGF9, TNRC9 |
Biliary tract cancer, Breast cancer, Breast neoplasm, Cancer, Cervical cancer, Colorectal cancer, Congenital esophageal anomaly, Endometrial cancer, Esophageal cancer, Estrogen-receptor negative breast cancer, Gastric cancer, Hepatocellular carcinoma, Insomnia, Liver neoplasm, Lung cancer, Metabolic syndrome, Neurotic disorder, Non-hodgkins lymphoma, Ovarian cancer, Ovarian serous carcinoma, Pancreatic cancer, Polycystic ovary syndrome, Prostate cancer, Willis-ekbom disease, Severe acute respiratory syndrome, Squamous cell carcinoma, Diabetes mellitus, type 2View all (12 more) |
|
252
|
|
|
Trinucleotide repeat containing adaptor 6A |
CAGH26, FAME6, GW1, GW182, TNRC6 |
Alzheimer disease, Atrial fibrillation, Attention deficit hyperactivity disorder, Autism, Obstructive pulmonary disease, Myoclonic epilepsy, Familial adult myoclonic epilepsy, Adult myoclonic epilepsy, Heart failure, Hypertension, Metabolic syndrome, Substance abuse, Diabetes mellitus, type 2 |
|
253
|
|
|
Transmembrane protein 97 |
MAC30, S2R, sigma2R |
|
|
254
|
|
|
Tripartite motif containing 49B |
- |
|
|
255
|
|
|
Tetratricopeptide repeat domain 9C |
- |
|
|
256
|
|
|
Transmembrane protein 114 |
- |
|
|
257
|
|
|
TRNA splicing endonuclease subunit 54 |
PCH2A, PCH4, PCH5, SEN54L, sen54 |
Amblyopia, Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay, Obstructive pulmonary disease, Congenital neurologic anomalies , Deglutition disorder, Global developmental delay, Intellectual developmental disorder, Methylmalonic acidemia, Microcephaly, Movement disorder, Pontocerebellar hypoplasia, Vissers-bodmer syndrome |
|
258
|
|
|
Transmembrane protein 235 |
ARGM1 |
|
|
259
|
|
|
Tubulin tyrosine ligase like 6 |
TTL.6 |
|
|
260
|
|
|
Transmembrane protein 150B |
DRAM3, TMEM224, TTN2 |
|
