CLEC4E C-type lectin domain family 4 member E
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Uncertain significance | 0 | 26 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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28 |
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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
[No Data.]
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 |
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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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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 | CLECSF9 |
SYNONYM | MINCLE |
MIM | 609962 OMIM |
HGNC | HGNC:14555 HGNC |
Ensembl | ENSG00000166523 Ensembl |
AllianceGenome | HGNC:14555 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000299663.8 | hg38 | chr12 | 8,533,305 | 8,540,905 | 7,601 |
ENST00000446457.6 | hg38 | chr12 | 8,534,484 | 8,540,877 | 6,394 |
ENST00000545274.5 | hg38 | chr12 | 8,534,509 | 8,540,873 | 6,365 |
ENST00000299663.8 | hg19 | chr12 | 8,685,901 | 8,693,501 | 7,601 |
ENST00000446457.6 | hg19 | chr12 | 8,687,080 | 8,693,473 | 6,394 |
ENST00000545274.5 | hg19 | chr12 | 8,687,105 | 8,693,469 | 6,365 |
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