CLEC2D C-type lectin domain family 2 member D
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
not provided | 10 | 0 |
Uncertain significance | 0 | 4 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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4 |
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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
Locus Zoom
Variants
Search Word
Target data | : |
MGeND data only
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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
Target data | : |
MGeND data only
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Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
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Category | : |
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Search word | : | |
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Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | CLAX |
SYNONYM | LLT1 |
SYNONYM | OCIL |
MIM | 605659 OMIM |
HGNC | HGNC:14351 HGNC |
Ensembl | ENSG00000069493 Ensembl |
AllianceGenome | HGNC:14351 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000261340.11 | hg38 | chr12 | 9,669,713 | 9,695,129 | 25,417 |
ENST00000545918.5 | hg38 | chr12 | 9,669,735 | 9,694,801 | 25,067 |
ENST00000261339.10 | hg38 | chr12 | 9,669,735 | 9,694,874 | 25,140 |
ENST00000290855.11 | hg38 | chr12 | 9,669,713 | 9,699,553 | 29,841 |
ENST00000543300.5 | hg38 | chr12 | 9,669,735 | 9,694,801 | 25,067 |
ENST00000261340.11 | hg19 | chr12 | 9,822,309 | 9,847,725 | 25,417 |
ENST00000290855.11 | hg19 | chr12 | 9,822,309 | 9,852,149 | 29,841 |
ENST00000543300.5 | hg19 | chr12 | 9,822,331 | 9,847,397 | 25,067 |
ENST00000545918.5 | hg19 | chr12 | 9,822,331 | 9,847,397 | 25,067 |
ENST00000261339.10 | hg19 | chr12 | 9,822,331 | 9,847,470 | 25,140 |
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