MTCH2 mitochondrial carrier 2

Information
Symbol
MTCH2
Type
protein-coding
Description
mitochondrial carrier 2
Entrez Gene ID
23788
Genome
hg19
Position
chr11:47,638,869-47,664,111
Genome
hg38
Position
chr11:47,617,317-47,642,559
MIM
613221 OMIM
HGNC
HGNC:17587 HGNC
Ensembl
ENSG00000109919 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 36
Ranking
ClinVar
0
0
0
36
0
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
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Variant name Gene AA change CDS Japanese
frequency		 TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence		 Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
SYNONYM HSPC032
SYNONYM MIMP
SYNONYM SLC25A50
MIM 613221 OMIM
HGNC HGNC:17587 HGNC
Ensembl ENSG00000109919 Ensembl
AllianceGenome HGNC:17587
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000530428.2 hg38 chr11 47,618,720 47,642,607 23,888
ENST00000302503.8 hg38 chr11 47,617,317 47,642,559 25,243
ENST00000302503.8 hg19 chr11 47,638,869 47,664,111 25,243
ENST00000530428.2 hg19 chr11 47,640,272 47,664,159 23,888
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