ITGAX integrin subunit alpha X

Information
Symbol
ITGAX
Type
protein-coding
Description
integrin subunit alpha X
Entrez Gene ID
3687
Genome
hg19
Position
chr16:31,366,543-31,394,264
Genome
hg38
Position
chr16:31,355,222-31,382,943
MIM
151510 OMIM
HGNC
HGNC:6152 HGNC
Ensembl
ENSG00000140678 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 8
Likely benign 0 26
Uncertain significance 0 134
Ranking
ClinVar
0
0
2
164
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 CD11C
SYNONYM SLEB6
MIM 151510 OMIM
HGNC HGNC:6152 HGNC
Ensembl ENSG00000140678 Ensembl
AllianceGenome HGNC:6152
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000562918.5 hg38 chr16 31,355,174 31,358,455 3,282
ENST00000562522.2 hg38 chr16 31,355,222 31,382,943 27,722
ENST00000268296.9 hg38 chr16 31,355,176 31,382,999 27,824
ENST00000562918.5 hg19 chr16 31,366,495 31,369,776 3,282
ENST00000268296.9 hg19 chr16 31,366,497 31,394,320 27,824
ENST00000562522.2 hg19 chr16 31,366,543 31,394,264 27,722
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