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MT-TK

Mitochondrially encoded tRNA lysine also known as MT-TK is a transfer RNA which in humans is encoded by the mitochondrial MT-TK gene.

Clinical significance, Function & Structure

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Clinical significance

35 related topics

Function

6 related topics

Structure

4 related topics

Overview

3 related topics

Key facts & relationships

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Alt. symbols
MERRF, MTTK
HGNC
7489
Locus
Chr. MT
NCBI gene
4566
RefSeq
NC_001807
Symbol
MT-TK

Topics to explore

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Overview

Structure

Function

Clinical significance

Advanced semantic analysis

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Map overview Semantic statistics

MT-TK

Nodes53
Edges52
Triples35
Avg. degree1.96
Density0.037736
Components1

How this topic connects Entity context

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MT-TK

Top relations

related to Myoclonic epilepsy with ragged-red fibers (MERRF) · 7
MT-TK → Another, Common, In, MERRF, Mutations, Myoclonic, The
related to Maternally inherited diabetes and deafness (MIDD) · 6
MT-TK → Additional, Diabetes, MIDD, Mutations, Researchers, The
related to Complex IV Deficiency · 4
MT-TK → Common, Cytochrome, IV, Other
related to Leigh syndrome · 4
MT-TK → Additional, Clinical, Leigh, The
related to Structure · 3
MT-TK → DNA, The, The MT-TK
related to Cardiomyopathy · 2
MT-TK → Additional, The
Alt. symbols · 1
MT-TK → MERRF, MTTK
HGNC · 1
MT-TK → 7489
Locus · 1
MT-TK → Chr. MT
NCBI gene · 1
MT-TK → 4566

Important terminology Word statistics

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Important terminology

gene merrf syndrome mutations symptoms mitochondrial include also epilepsy myopathy disorder found ragged-red diabetes cardiomyopathy heart cause mutation may known

Entity relationships Subject–Predicate–Object triples

SubjectPredicateObjectConfidenceSrc
MT-TKAlt. symbolsMERRF, MTTK1.00infobox
MT-TKHGNC74891.00infobox
MT-TKLocusChr. MT1.00infobox
MT-TKNCBI gene45661.00infobox
MT-TKRefSeqNC_0018071.00infobox
MT-TKSymbolMT-TK1.00infobox
MT-TKis atransfer RNA which in humans is encoded by the mitochondrial MT-TK gene0.90text
MT-TKrelated to CardiomyopathyThe0.60section
MT-TKrelated to CardiomyopathyAdditional0.60section
MT-TKrelated to Clinical significanceMutations0.60section
MT-TKrelated to Complex IV DeficiencyIV0.60section
MT-TKrelated to Complex IV DeficiencyCytochrome0.60section

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    Min side: 3
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