Genesⓘ

Dataset:
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "T"
381 to 390 of 913 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

381
Transient receptor potential cation channel subfamily M member 4
EKVP6, LTrpC4, PFHB1B, TRPM4B, hTRPM4
Atrioventricular block, Brugada syndrome, Bundle branch block, Congestive heart failure, Erythrokeratodermia variabilis, Heart block, Hereditary bundle branch system defect, Left anterior fascicular block, Palmoplantar keratoderma, Paroxysmal ventricular tachycardia, Progressive cardiac conduction defect, Progressive symmetric erythrokeratodermia, Prostatic neoplasms, Prostate cancer, Sick sinus syndrome
View all (3 more)

382
TRNA isopentenyltransferase 1
COXPD35, GRO1, IPPT, IPT, IPTase, MOD5, hGRO1
Cerebral atrophy, Combined oxidative phosphorylation deficiency, Developmental delay, Epileptic encephalopathy, Esotropia, Mental retardation, Microcephaly, Myoclonic seizures, Myopia

383
Transient receptor potential cation channel subfamily M member 7
ALSPDC, CHAK, CHAK1, LTRPC7, LTrpC-7, TRP-PLIK
Adenoma, Amyotrophic lateral sclerosis, Bulbar palsy, Colorectal cancer, Colorectal neoplasms, Dementia, Gastric cancer, Guam parkinsonism dementia complex, Immune system diseases, Infiltrating duct carcinoma of female breast, Kidney stone, Liver cirrhosis, Liver fibrosis, Macrothrombocytopenia, Ovarian serous adenocarcinoma
View all (2 more)

384
TBC1 domain family member 8B
GRAMD8B, NPHS20
Genetic steroid-resistant nephrotic syndrome, Glomerulosclerosis, Kidney disease, Nephritis, Nephrotic syndrome, Steroid resistant nephrotic syndrome

385
Tetratricopeptide repeat domain 19
2010204O13Rik, MC3DN2
Anxiety disorder, Apraxia, Cerebellar atrophy, Cerebral atrophy, Degenerative diseases, central nervous system, Dysarthria, Gait disturbance, Hallucinations, Impaired cognition, Isolated complex iii deficiency, Leigh syndrome, Mental depression, Mitochondrial complex deficiency, Mitochondrial diseases, Necrotizing encephalomyelopathy
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386
Transcription activation suppressor family member 2
C10orf18, FAM208B, bA318E3.2
Breast carcinoma, Malignant melanoma of skin, Melanoma

387
Transmembrane protein 260
C14orf101, SHDRA
Leukemia, Partial agenesis of corpus callosum, Persistent truncus arteriosus, Renal insufficiency, Structural heart defects and renal anomalies syndrome, Ventricular septal defect

388
Transmembrane protein 161A
AROS-29, AROS29
Breast cancer

389
TRNA methyltransferase 10C, mitochondrial RNase P subunit
COXPD30, HNYA, MRPP1, RG9MTD1
Combined oxidative phosphorylation deficiency, Gastroesophageal reflux disease, Mitochondrial diseases

390
Thioredoxin like 4B
DLP, Dim2
Anhaptoglobinemia, Cardiovascular diseases, Diabetes mellitus