SELL selectin L

Information
Symbol
SELL
Type
protein-coding
Description
selectin L
Entrez Gene ID
6402
Genome
hg19
Position
chr1:169,659,808-169,680,761
Genome
hg38
Position
chr1:169,690,667-169,711,620
MIM
153240 OMIM
HGNC
HGNC:10720 HGNC
Ensembl
ENSG00000188404 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 8
Likely benign 0 2
Uncertain significance 0 26
Ranking
ClinVar
0
0
0
36
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 :
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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 CD62L
SYNONYM LAM1
SYNONYM LECAM1
SYNONYM LEU8
SYNONYM LNHR
SYNONYM LSEL
SYNONYM LYAM1
SYNONYM PLNHR
SYNONYM TQ1
MIM 153240 OMIM
HGNC HGNC:10720 HGNC
Ensembl ENSG00000188404 Ensembl
AllianceGenome HGNC:10720
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000650983.1 hg38 chr1 169,690,665 169,711,702 21,038
ENST00000236147.6 hg38 chr1 169,690,667 169,711,620 20,954
ENST00000650983.1 hg19 chr1 169,659,806 169,680,843 21,038
ENST00000236147.6 hg19 chr1 169,659,808 169,680,761 20,954
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