ITGA2B integrin subunit alpha 2b

Information
Symbol
ITGA2B
Type
protein-coding
Description
integrin subunit alpha 2b
Entrez Gene ID
3674
Genome
hg19
Position
chr17:42,449,549-42,467,017
Genome
hg38
Position
chr17:44,372,181-44,389,649
MIM
607759 OMIM
HGNC
HGNC:6138 HGNC
Ensembl
ENSG00000005961 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 266
Likely pathogenic 0 190
Benign 0 72
Likely benign 0 272
Conflicting classifications of pathogenicity 0 26
Uncertain significance 0 552
Ranking
ClinVar
0
606
90
622
22
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 BDPLT16
SYNONYM BDPLT2
SYNONYM CD41
SYNONYM CD41B
SYNONYM GP2B
SYNONYM GPIIb
SYNONYM GT
SYNONYM GT1
SYNONYM GTA
SYNONYM HPA3
SYNONYM PPP1R93
MIM 607759 OMIM
HGNC HGNC:6138 HGNC
Ensembl ENSG00000005961 Ensembl
AllianceGenome HGNC:6138
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000262407.6 hg38 chr17 44,372,181 44,389,649 17,469
ENST00000262407.6 hg19 chr17 42,449,549 42,467,017 17,469
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