SELPLG selectin P ligand

Information
Symbol
SELPLG
Type
protein-coding
Description
selectin P ligand
Entrez Gene ID
6404
Genome
hg19
Position
chr12:109,016,605-109,025,854
Genome
hg38
Position
chr12:108,622,829-108,632,078
MIM
600738 OMIM
HGNC
HGNC:10722 HGNC
Ensembl
ENSG00000110876 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 8
Likely benign 0 18
Uncertain significance 0 44
Ranking
ClinVar
0
0
2
68
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 CD162
SYNONYM CLA
SYNONYM PSGL-1
SYNONYM PSGL1
MIM 600738 OMIM
HGNC HGNC:10722 HGNC
Ensembl ENSG00000110876 Ensembl
AllianceGenome HGNC:10722
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000228463.6 hg38 chr12 108,622,829 108,632,078 9,250
ENST00000388962.4 hg38 chr12 108,622,688 108,624,330 1,643
ENST00000550948.2 hg38 chr12 108,621,895 108,633,894 12,000
ENST00000550948.2 hg19 chr12 109,015,671 109,027,670 12,000
ENST00000388962.4 hg19 chr12 109,016,464 109,018,106 1,643
ENST00000228463.6 hg19 chr12 109,016,605 109,025,854 9,250
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