CLECL1P C-type lectin like 1, pseudogene
Clinical Significance
MGeND | ClinVar |
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Ranking
ClinVar | |
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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 |
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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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 |
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Target data | : |
MGeND data only
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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 | CLECL1 |
SYNONYM | DCAL-1 |
SYNONYM | DCAL1 |
MIM | 607467 OMIM |
HGNC | HGNC:24462 HGNC |
Ensembl | ENSG00000293488 Ensembl |
AllianceGenome | HGNC:24462 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000540988.1 | hg38 | chr12 | 9,715,860 | 9,722,661 | 6,802 |
ENST00000702603.1 | hg38 | chr12 | 9,702,182 | 9,733,097 | 30,916 |
ENST00000702603.1 | hg19 | chr12 | 9,854,778 | 9,885,693 | 30,916 |
ENST00000540988.1 | hg19 | chr12 | 9,868,456 | 9,875,257 | 6,802 |
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