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MSeqDR-LSDB: Mitochondrial Disease LSDB
General information
Gene symbol MT-TK
Gene name mitochondrially encoded tRNA lysine
Chromosome M
Chromosomal band M
Imprinted
Genomic reference NC_012920.1
Transcript reference MT-TK-201
Associated with diseases 556500, LS, MELAS SYNDROME, MERRF, MIDD, MTDPS1
Citation reference(s) -
Curators (5) Lishuang Shen, Marni J Falk, L Shen, Xiaowu Gai and UMDF15
Total number of public variants reported 23
Unique public DNA variants reported 23
Individuals with public variants 0
Hidden variants 0
Notes MSeqDR-LSDB
Date created November 12, 2013
Date last updated November 30, -0001
Version MT-TK:-11130

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
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Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
HGNC 7489
Entrez Gene 4566
PubMed articles MT-TK
OMIM - Gene 590060
OMIM - Diseases 556500 (PARKINSON DISEASE, MITOCHONDRIAL )
LS (Leigh syndrome due to mitochondrial complex 1 deficiency, 256000 (3))
MELAS SYNDROME (MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC ACIDOSIS, AND STROKE-LIKE EPISODES)
MERRF (MYOCLONIC EPILEPSY ASSOCIATED WITH RAGGED-RED FIBERS)
MIDD (DIABETES AND DEAFNESS, MATERNALLY INHERITED)
MTDPS1 (Mitochondrial DNA depletion syndrome 1 (MNGIE type), 603041 (3))
HGMD MT-TK
GeneCards MT-TK
GeneTests MT-TK


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00001335 M MT-TK-201 MT-TK-201 - 23


Copyright & disclaimer
Mitochondria chromosome located genes from HGNC

Mitochondrial Disease Sequence Data Resource (MSeqDR) Consortium