Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
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
Alzheimer disease, Arrhythmogenic right ventricular cardiomyopathy, Atrioventricular block, Brugada syndrome, Cardiac arrest, Cardiac conduction disease, Cardiomyopathy, Erythrokeratodermia variabilis, Heart failure, Hereditary bundle branch system defect, Hypertrophic cardiomyopathy, Long qt syndrome, Prostatic neoplasm, Short qt syndrome, Ventricular fibrillation
View all (2 more)

382
TRNA isopentenyltransferase 1
COXPD35, GRO1, IPPT, IPT, IPTase, MOD5, hGRO1
Androgenetic alopecia, Combined oxidative phosphorylation deficiency, Developmental and epileptic encephalopathy, Major depressive disorder, Mitochondrial disease

383
Transient receptor potential cation channel subfamily M member 7
ALSPDC, CHAK, CHAK1, LTRPC7, LTrpC-7, TRP-PLIK
Amyotrophic lateral sclerosis, Macrothrombocytopenia, Central nervous system cancer, Colorectal neoplasm, Coronary artery disease, Glioblastoma, Glioma, Immune system disease, Liver cirrhosis, Paralysis, Parkinson-dementia complex of guam

384
TBC1 domain family member 8B
GRAMD8B, NPHS20
Idiopathic steroid-resistant nephrotic syndrome, Genetic steroid-resistant nephrotic syndrome, Steroid-resistant nephrotic syndrome, Nephrotic syndrome, Pancreatitis

385
Tetratricopeptide repeat domain 19
2010204O13Rik, MC3DN2
Asthma, Autism, Degenerative disorder, Infertility, Leigh syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Nervous system disease, Neurodegenerative disorders

386
Transcription activation suppressor family member 2
C10orf18, FAM208B, bA318E3.2
Breast cancer, Melanoma, Osteosarcoma, Prostate cancer

387
Transmembrane protein 260
C14orf101, SHDRA

388
Transmembrane protein 161A
AROS-29, AROS29
Cholangiocarcinoma, Willis-ekbom disease

389
TRNA methyltransferase 10C, mitochondrial RNase P subunit
COXPD30, HNYA, MRPP1, RG9MTD1
Asthma, Eczema, Basal cell carcinoma, Combined oxidative phosphorylation deficiency, Major depressive disorder, Mitochondrial disease

390
Thioredoxin like 4B
DLP, Dim2