Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "T"
761 to 770 of 1188 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

761
Translocase of outer mitochondrial membrane 20
MAS20, MOM19, TOM20
Obesity

762
Translocase of outer mitochondrial membrane 40
C19orf1, D19S1177E, PER-EC1, PEREC1, TOM40
Alzheimer disease, Cardiovascular disease, Ischemic stroke, Coronary artery disease, Dyslipidemias, Glaucoma, Hyperlipidemia, Insomnia, Lewy body disease, Major depressive disorder, Metabolic syndrome, Posterior cortical atrophy, Sarcoidosis, Diabetes mellitus type 2, Depression
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763
Translocase of outer mitochondrial membrane 40 like
TOMM40B
Iga nephropathy

764
Translocase of outer mitochondrial membrane 5
C9orf105, Tom5, bA613M10.3
Sarcoidosis, Schizophrenia

765
Translocase of outer mitochondrial membrane 7
GMPGS, TOM7
Aortic stenosis, Aortic valve disease, Asthma, Eczema, Atrial fibrillation, Auditory system disease, Oligoarticular juvenile idiopathic arthritis, Polyarticular juvenile idiopathic arthritis, Juvenile idiopathic arthritis, Diabetes mellitus type 2

766
Translocase of outer mitochondrial membrane 70
TOMM70A, Tom70
Combined oxidative phosphorylation deficiency, Leukodystrophy, Mitochondrial disease, Nervous system disease

767
Transmembrane O-methyltransferase
COMT2
Deafness, Hearing impairment

768
Tonsoku like, DNA repair protein
IKBR, NFKBIL2, SEMDSP
Hepatocellular carcinoma, Desbuquois syndrome, Ovarian epithelial cancer, Ovarian cancer, Polycystic ovary syndrome, Spondyloepimetaphyseal dysplasia, Spondylometaphyseal dysplasia

769
DNA topoisomerase I
TOPI
Autism, Cataract, Gout, Liver neoplasms, Myocardial infarction, Ovarian neoplasms

770
DNA topoisomerase I mitochondrial
-
Metabolic syndrome, Hearing loss, Diabetes mellitus type 2