Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
4568
Gene name Gene Name - the full gene name approved by the HGNC.
Mitochondrially encoded tRNA leucine 2 (CUN)
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
TRNL2
Synonyms (NCBI Gene) Gene synonyms aliases
MTTL2
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
590055 7491 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
Hypothyroidism Hypothyroidism rs869320723, rs121908862, rs121908863, rs121908865, rs121908866, rs121908867, rs121908870, rs121908871, rs121908872, rs2140110277, rs121908881, rs121908884, rs121908885, rs786205080, rs1586182912
View all (22 more)
Mental retardation Mild Mental Retardation rs5742905, rs267607136, rs267607137, rs2131714307, rs267607038, rs267607042, rs80338685, rs137853127, rs80338815, rs28940893, rs387906309, rs121908096, rs121908099, rs587784365, rs121918315
View all (1024 more)
Mitochondrial encephalomyopathy Mitochondrial Encephalomyopathies rs121434462, rs199474661, rs121434456, rs207459999, rs387906731, rs387906736
Mitochondrial myopathy Mitochondrial Myopathies rs121434454
Unknown
Disease term Disease name Evidence References Source
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
Atherosclerosis Associate 22997526
Cysts Associate 37674615
Diabetes Mellitus Associate 23696415
Mitochondrial Diseases Associate 29052516
Mitochondrial Myopathies Associate 25223649
Multiple Sclerosis Associate 36534684
Muscular Diseases Associate 29052516
Myopathy with Lactic Acidosis Hereditary Associate 29052516
Ophthalmoplegia Associate 29052516
Ophthalmoplegia Chronic Progressive External Associate 32310184