MT-TK gene homepage

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, 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
Download all this gene's data	Download all data
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 »
UCSC Genome Browser	Show variants in the UCSC Genome Browser (full view, compact view)
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 ) 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

Legend

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ID	Chr	Name	NCBI ID	NCBI Protein ID	Variants
00001335	M	MT-TK-201	MT-TK-201	-	23

Copyright & disclaimer
Mitochondria chromosome located genes from HGNC

Mitochondrial Disease Sequence Data Resource (MSeqDR) Consortium