ITGA7 integrin subunit alpha 7

Information
Symbol
ITGA7
Type
protein-coding
Description
integrin subunit alpha 7
Entrez Gene ID
3679
Genome
hg19
Position
chr12:56,078,487-56,101,495
Genome
hg38
Position
chr12:55,684,703-55,707,711
MIM
600536 OMIM
HGNC
HGNC:6143 HGNC
Ensembl
ENSG00000135424 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 68
Likely pathogenic 0 56
Benign 0 170
Likely benign 0 742
Conflicting classifications of pathogenicity 0 46
Uncertain significance 0 880
Ranking
ClinVar
0
0
412
1,436
6
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 :
Filtering :
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
MIM 600536 OMIM
HGNC HGNC:6143 HGNC
Ensembl ENSG00000135424 Ensembl
AllianceGenome HGNC:6143
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000553804.6 hg38 chr12 55,684,568 55,707,904 23,337
ENST00000347027.10 hg38 chr12 55,684,572 55,707,884 23,313
ENST00000557555.3 hg38 chr12 55,684,858 55,707,682 22,825
ENST00000557257.2 hg38 chr12 55,685,058 55,712,118 27,061
ENST00000555728.5 hg38 chr12 55,684,703 55,707,711 23,009
ENST00000452168.6 hg38 chr12 55,684,572 55,712,411 27,840
ENST00000691973.1 hg38 chr12 55,684,601 55,707,682 23,082
ENST00000257879.11 hg38 chr12 55,684,568 55,707,904 23,337
ENST00000553804.6 hg19 chr12 56,078,352 56,101,688 23,337
ENST00000257879.11 hg19 chr12 56,078,352 56,101,688 23,337
ENST00000347027.10 hg19 chr12 56,078,356 56,101,668 23,313
ENST00000452168.6 hg19 chr12 56,078,356 56,106,195 27,840
ENST00000555728.5 hg19 chr12 56,078,487 56,101,495 23,009
ENST00000557257.2 hg19 chr12 56,078,842 56,105,902 27,061
ENST00000557555.3 hg19 chr12 56,078,642 56,101,466 22,825
ENST00000691973.1 hg19 chr12 56,078,385 56,101,466 23,082
Genome browser