CD22 CD22 molecule

Information
Symbol
CD22
Type
protein-coding
Description
CD22 molecule
Entrez Gene ID
933
Genome
hg19
Position
chr19:35,820,090-35,838,264
Genome
hg38
Position
chr19:35,329,187-35,347,361
MIM
107266 OMIM
HGNC
HGNC:1643 HGNC
Ensembl
ENSG00000012124 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 8
Likely benign 0 18
Uncertain significance 0 92
Ranking
ClinVar
0
0
0
118
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 SIGLEC-2
SYNONYM SIGLEC2
MIM 107266 OMIM
HGNC HGNC:1643 HGNC
Ensembl ENSG00000012124 Ensembl
AllianceGenome HGNC:1643
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000594250.5 hg38 chr19 35,332,016 35,346,766 14,751
ENST00000341773.10 hg38 chr19 35,329,169 35,347,355 18,187
ENST00000544992.6 hg38 chr19 35,329,212 35,346,929 17,718
ENST00000536635.6 hg38 chr19 35,329,187 35,347,355 18,169
ENST00000419549.6 hg38 chr19 35,329,212 35,346,929 17,718
ENST00000085219.10 hg38 chr19 35,329,187 35,347,361 18,175
ENST00000085219.10 hg19 chr19 35,820,090 35,838,264 18,175
ENST00000341773.10 hg19 chr19 35,820,072 35,838,258 18,187
ENST00000544992.6 hg19 chr19 35,820,115 35,837,832 17,718
ENST00000419549.6 hg19 chr19 35,820,115 35,837,832 17,718
ENST00000594250.5 hg19 chr19 35,822,919 35,837,669 14,751
ENST00000536635.6 hg19 chr19 35,820,090 35,838,258 18,169
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