CLEC4M C-type lectin domain family 4 member M

Information
Symbol
CLEC4M
Type
protein-coding
Description
C-type lectin domain family 4 member M
Entrez Gene ID
10332
Genome
hg19
Position
chr19:7,828,129-7,834,491
Genome
hg38
Position
chr19:7,763,243-7,769,605
MIM
605872 OMIM
HGNC
HGNC:13523 HGNC
Ensembl
ENSG00000104938 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 10
Uncertain significance 0 28
Ranking
ClinVar
0
0
0
38
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 CD209L
SYNONYM CD299
SYNONYM DC-SIGN2
SYNONYM DC-SIGNR
SYNONYM DCSIGNR
SYNONYM HP10347
SYNONYM L-SIGN
SYNONYM LSIGN
MIM 605872 OMIM
HGNC HGNC:13523 HGNC
Ensembl ENSG00000104938 Ensembl
AllianceGenome HGNC:13523
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000596363.5 hg38 chr19 7,763,217 7,769,604 6,388
ENST00000394122.7 hg38 chr19 7,763,241 7,769,604 6,364
ENST00000327325.10 hg38 chr19 7,763,243 7,769,605 6,363
ENST00000596363.5 hg19 chr19 7,828,103 7,834,490 6,388
ENST00000394122.7 hg19 chr19 7,828,127 7,834,490 6,364
ENST00000327325.10 hg19 chr19 7,828,129 7,834,491 6,363
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