Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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14011 to 14020 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

14011
TRNA aspartic acid methyltransferase 1
DMNT2, DNMT2, MHSAIIP, PUMET, RNMT1
Cervical cancer

14012
Triadin
CARDAR, CPVT5, TDN, TRISK
Cardiac arrhythmias, Breast cancer, Cardiac arrhythmia, Catecholaminergic polymorphic ventricular tachycardia, Central nervous system cancer, Color vision deficiency, Diabetic foot, Endometriosis, Long qt syndrome, Glioblastoma, Glioma, Heart failure, Hypertension, Hypertrophic cardiomyopathy, Neuropathy
View all (1 more)

14013
Trehalase
TRE, TREA, TREHD
Trehalase deficiency

14014
Triggering receptor expressed on myeloid cells 1
CD354, TREM-1
Alzheimer disease, Liver disease, Schizophrenia, Sepsis

14015
Triggering receptor expressed on myeloid cells 2
AD17, PLOSL2, TREM-2, Trem2a, Trem2b, Trem2c
Alzheimer disease, Amyotrophic lateral sclerosis, Aortic stenosis, Aortic valve disease, Dementia, Desbuquois syndrome, Frontotemporal dementia, Nasopharyngeal neoplasms, Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy

14016
Triggering receptor expressed on myeloid cells like 1
GLTL1825, PRO3438, TLT-1, TLT1, dJ238O23.3
Juvenile arthritis, Juvenile idiopathic arthritis, Oligoarticular juvenile idiopathic arthritis

14017
Triggering receptor expressed on myeloid cells like 2
C6orf76, TLT-2, TLT2, dJ238O23.1
Alzheimer disease, Aortic stenosis, Aortic valve disease, Dementia, Lewy body disease, Diabetes mellitus type 2

14018
Transcriptional regulating factor 1
BCAR2, HSA277276, RAPA, TREP132, TReP-132, dJ139D8.5
Breast neoplasms, Neurodevelopmental disorder, Non-specific syndromic intellectual disability

14019
Three prime repair exonuclease 1
AGS1, CRV, DRN3, HERNS, RVCLS
Aicardi goutieres syndrome, Brain disease, Cadasil, Chilblain lupus erythematosus, Vascular dementia, Chilblain lupus, Systemic lupus erythematosus, Neurodevelopmental disorder, Obesity, Retinitis pigmentosa, Type i interferonopathy, Retinal vasculopathy with cerebral leukodystrophy

14020
Three prime repair exonuclease 2
-
Intellectual developmental disorder