Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
4576
Gene name Gene Name - the full gene name approved by the HGNC.
Mitochondrially encoded tRNA threonine
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
TRNT
Synonyms (NCBI Gene) Gene synonyms aliases
MTTT
Chromosome Chromosome number
MT
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
-
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
590090 7499 HGNC
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  
  Aminoacyl-tRNA biosynthesis  
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Cardiomyopathy Cardiomyopathies rs267607003, rs267607002, rs267607004, rs63750743, rs121908333, rs121908334, rs104894655, rs121434420, rs121434421, rs193922674, rs111517471, rs121908987, rs193922384, rs121909374, rs121909377
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Merrf syndrome MERRF Syndrome rs118203886, rs118192098, rs118192099, rs118192100, rs118192104, rs199474659, rs121434470, rs267606898, rs1603225633, rs1603219393
Mitochondrial myopathy MITOCHONDRIAL MYOPATHY, LETHAL, INFANTILE rs121434454 1645537
Myopathy Myopathy rs137854521, rs386834236, rs121908557, rs121909092, rs111033570, rs104894299, rs104894294, rs121909273, rs121909274, rs121909275, rs199474699, rs199476140, rs118192165, rs118192169, rs118192166
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Unknown
Disease term Disease name Evidence References Source
Progressive external ophthalmoplegia Chronic progressive external ophthalmoplegia ClinVar
Associations from Text Mining
Disease Name Relationship Type References
MERRF Syndrome Associate 30236074
Methylcobalamin Deficiency CblG Type Inhibit 38168585
Mitochondrial Diseases Associate 28187756
Muscular Diseases Associate 30236074