Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
4570
Gene name Gene Name - the full gene name approved by the HGNC.
Mitochondrially encoded tRNA asparagine
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
TRNN
Synonyms (NCBI Gene) Gene synonyms aliases
MTTN
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
590010 7493 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
Anemia Anemia rs118204044, rs118204045, rs118204046, rs121918330, rs869320719, rs869312029, rs121918332, rs869320724, rs767094129, rs786205058, rs786205059, rs137853119, rs137853120, rs137853121, rs1384933966
View all (89 more)
Developmental delay Global developmental delay rs28941770, rs199469464, rs281865469, rs143747297, rs398123009, rs587777428, rs786205133, rs606231459, rs797044854, rs797045027, rs864309504, rs878853160, rs886039902, rs886042046, rs886041291
View all (32 more)
External ophthalmoplegia External Ophthalmoplegia rs1569484022
Fanconi syndrome Adult Fanconi syndrome rs398124646
Unknown
Disease term Disease name Evidence References Source
Cytochrome-c oxidase deficiency Cytochrome-c Oxidase Deficiency ClinVar
Mental depression Depressive disorder ClinVar
Progressive external ophthalmoplegia Chronic progressive external ophthalmoplegia 23696415 ClinVar
Ptosis Blepharoptosis, Ptosis ClinVar
Associations from Text Mining
Disease Name Relationship Type References
Aicardi Goutieres syndrome Associate 38320662
Brain Diseases Associate 38320662
Mitochondrial Diseases Inhibit 38320662
Mitochondrial encephalopathy Associate 38320662