Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
4577
Gene name Gene Name - the full gene name approved by the HGNC.
Mitochondrially encoded tRNA valine
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
TRNV
Synonyms (NCBI Gene) Gene synonyms aliases
MTTV
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
590105 7500 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 Cardiomyopathy, Dilated rs267607003, rs267607002, rs267607004, rs63750743, rs121908333, rs121908334, rs104894655, rs121434420, rs121434421, rs193922674, rs111517471, rs121908987, rs193922384, rs121909374, rs121909377
View all (900 more)
Developmental regression Developmental regression rs1224421127
Diabetes mellitus Diabetes Mellitus rs587776515, rs61730328, rs606231121, rs606231122, rs79020217, rs77625743, rs78378398, rs606231123, rs1362648752, rs104893649, rs80356624, rs80356616, rs80356625, rs80356611, rs104894237
View all (293 more)
Epileptic encephalopathy Encephalopathies rs587776508, rs121918334, rs121918317, rs121918321, rs74315390, rs28939684, rs74315391, rs74315392, rs118192244, rs121918622, rs121918623, rs121917953, rs121917955, rs121918624, rs121918625
View all (860 more)
Unknown
Disease term Disease name Evidence References Source
Congestive heart failure Congestive heart failure ClinVar
Associations from Text Mining
Disease Name Relationship Type References
Brain Diseases Associate 24691472
Cytochrome c Oxidase Deficiency Associate 24691472
Growth Disorders Associate 21540128
Hearing Loss Associate 21540128
Leigh Disease Associate 24691472
Metabolic Diseases Associate 18400783
Respiratory System Abnormalities Associate 24691472
Stroke Associate 21540128
Visceral myopathy familial external ophthalmoplegia Associate 21540128