COX7A2L cytochrome c oxidase subunit 7A2 like

Information
Symbol
COX7A2L
Type
protein-coding
Description
cytochrome c oxidase subunit 7A2 like
Entrez Gene ID
9167
Genome
hg19
Position
chr2:42,576,478-42,596,150
Genome
hg38
Position
chr2:42,349,338-42,369,010
MIM
605771 OMIM
HGNC
HGNC:2289 HGNC
Ensembl
ENSG00000115944 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 8
Ranking
ClinVar
0
0
0
8
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
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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 COX7AR
SYNONYM COX7RP
SYNONYM EB1
SYNONYM SCAF1
SYNONYM SCAFI
SYNONYM SIG81
MIM 605771 OMIM
HGNC HGNC:2289 HGNC
Ensembl ENSG00000115944 Ensembl
AllianceGenome HGNC:2289
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000378669.5 hg38 chr2 42,349,338 42,369,010 19,673
ENST00000234301.3 hg38 chr2 42,349,338 42,361,217 11,880
ENST00000463055.1 hg38 chr2 42,352,887 42,361,172 8,286
ENST00000234301.3 hg19 chr2 42,576,478 42,588,357 11,880
ENST00000378669.5 hg19 chr2 42,576,478 42,596,150 19,673
ENST00000463055.1 hg19 chr2 42,580,027 42,588,312 8,286
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