CLEC18A C-type lectin domain family 18 member A

Information
Symbol
CLEC18A
Type
protein-coding
Description
C-type lectin domain family 18 member A
Entrez Gene ID
348174
Genome
hg19
Position
chr16:69,984,810-69,997,889
Genome
hg38
Position
chr16:69,950,907-69,963,986
MIM
616571 OMIM
HGNC
HGNC:30388 HGNC
Ensembl
ENSG00000157322 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 8
Uncertain significance 0 54
Ranking
ClinVar
0
0
0
62
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 MRCL
SYNONYM MRCL1
SYNONYM MRLP2
MIM 616571 OMIM
HGNC HGNC:30388 HGNC
Ensembl ENSG00000157322 Ensembl
AllianceGenome HGNC:30388
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000449317.6 hg38 chr16 69,951,233 69,963,984 12,752
ENST00000568461.5 hg38 chr16 69,950,986 69,963,986 13,001
ENST00000393701.6 hg38 chr16 69,950,907 69,963,986 13,080
ENST00000288040.11 hg38 chr16 69,951,334 69,963,986 12,653
ENST00000615430.4 hg38 chr16 69,950,705 69,964,347 13,643
ENST00000615430.4 hg19 chr16 69,984,608 69,998,250 13,643
ENST00000393701.6 hg19 chr16 69,984,810 69,997,889 13,080
ENST00000568461.5 hg19 chr16 69,984,889 69,997,889 13,001
ENST00000449317.6 hg19 chr16 69,985,136 69,997,887 12,752
ENST00000288040.11 hg19 chr16 69,985,237 69,997,889 12,653
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