CD209 CD209 molecule

Information
Symbol
CD209
Type
protein-coding
Description
CD209 molecule
Entrez Gene ID
30835
Genome
hg19
Position
chr19:7,804,879-7,812,420
Genome
hg38
Position
chr19:7,739,993-7,747,534
MIM
604672 OMIM
HGNC
HGNC:1641 HGNC
Ensembl
ENSG00000090659 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 10
Likely benign 0 16
Conflicting classifications of pathogenicity 0 2
Uncertain significance 0 28
Ranking
ClinVar
0
0
2
52
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 :
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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 CDSIGN
SYNONYM CLEC4L
SYNONYM DC-SIGN
SYNONYM DC-SIGN1
SYNONYM hDC-SIGN
MIM 604672 OMIM
HGNC HGNC:1641 HGNC
Ensembl ENSG00000090659 Ensembl
AllianceGenome HGNC:1641
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000315599.12 hg38 chr19 7,739,993 7,747,534 7,542
ENST00000204801.12 hg38 chr19 7,743,039 7,747,511 4,473
ENST00000394173.8 hg38 chr19 7,742,511 7,747,564 5,054
ENST00000354397.10 hg38 chr19 7,743,039 7,747,511 4,473
ENST00000315591.12 hg38 chr19 7,743,039 7,747,511 4,473
ENST00000593660.5 hg38 chr19 7,742,647 7,747,511 4,865
ENST00000394161.9 hg38 chr19 7,743,039 7,747,511 4,473
ENST00000601951.5 hg38 chr19 7,742,850 7,747,518 4,669
ENST00000593821.5 hg38 chr19 7,743,039 7,747,511 4,473
ENST00000601256.1 hg38 chr19 7,743,175 7,747,511 4,337
ENST00000602261.5 hg38 chr19 7,743,039 7,747,511 4,473
ENST00000315599.12 hg19 chr19 7,804,879 7,812,420 7,542
ENST00000394173.8 hg19 chr19 7,807,397 7,812,450 5,054
ENST00000593660.5 hg19 chr19 7,807,533 7,812,397 4,865
ENST00000601951.5 hg19 chr19 7,807,736 7,812,404 4,669
ENST00000204801.12 hg19 chr19 7,807,925 7,812,397 4,473
ENST00000315591.12 hg19 chr19 7,807,925 7,812,397 4,473
ENST00000354397.10 hg19 chr19 7,807,925 7,812,397 4,473
ENST00000394161.9 hg19 chr19 7,807,925 7,812,397 4,473
ENST00000593821.5 hg19 chr19 7,807,925 7,812,397 4,473
ENST00000602261.5 hg19 chr19 7,807,925 7,812,397 4,473
ENST00000601256.1 hg19 chr19 7,808,061 7,812,397 4,337
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