ITGA4 integrin subunit alpha 4

Information
Symbol
ITGA4
Type
protein-coding
Description
integrin subunit alpha 4
Entrez Gene ID
3676
Genome
hg19
Position
chr2:182,322,113-182,403,667
Genome
hg38
Position
chr2:181,457,386-181,538,940
MIM
192975 OMIM
HGNC
HGNC:6140 HGNC
Ensembl
ENSG00000115232 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely pathogenic 0 6
Benign 0 34
Likely benign 0 90
Conflicting classifications of pathogenicity 0 14
Uncertain significance 0 180
Ranking
ClinVar
0
0
20
288
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 :
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
SYNONYM CD49D
SYNONYM IA4
MIM 192975 OMIM
HGNC HGNC:6140 HGNC
Ensembl ENSG00000115232 Ensembl
AllianceGenome HGNC:6140
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000339307.8 hg38 chr2 181,457,207 181,476,218 19,012
ENST00000397033.7 hg38 chr2 181,457,386 181,538,940 81,555
ENST00000339307.8 hg19 chr2 182,321,934 182,340,945 19,012
ENST00000397033.7 hg19 chr2 182,322,113 182,403,667 81,555
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