Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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13891 to 13900 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

13891
Toll interacting protein
IL-1RAcPIP
Obstructive airway disease, Idiopathic pulmonary fibrosis, Interstitial lung disease

13892
Target of myb1 membrane trafficking protein
IMD85
Bipolar disorder, Crohn disease, Immune system disease, Immunodeficiency, Inflammatory bowel disease, Major depressive disorder, Multiple myeloma, Psoriasis, Diabetes mellitus type 2, Ulcerative colitis

13893
Target of myb1 like 1 membrane trafficking protein
SRCASM
Dementia, Large artery stroke, Metabolic syndrome, Obesity, Prostatic neoplasms, Stroke, Diabetes mellitus type 2

13894
Target of myb1 like 2 membrane trafficking protein
-
Colorectal cancer, Coronary artery disease, Dementia, Myocardial infarction, Prostate cancer, Diabetes mellitus type 2

13895
Translocase of outer mitochondrial membrane 20
MAS20, MOM19, TOM20
Obesity

13896
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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13897
Translocase of outer mitochondrial membrane 40 like
TOMM40B
Iga nephropathy

13898
Translocase of outer mitochondrial membrane 5
C9orf105, Tom5, bA613M10.3
Sarcoidosis, Schizophrenia

13899
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

13900
Translocase of outer mitochondrial membrane 70
TOMM70A, Tom70
Combined oxidative phosphorylation deficiency, Leukodystrophy, Mitochondrial disease, Nervous system disease