LRP4 LDL receptor related protein 4
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 30 |
Likely pathogenic | 0 | 28 |
Benign | 0 | 200 |
Likely benign | 0 | 894 |
Conflicting classifications of pathogenicity | 0 | 94 |
Uncertain significance | 0 | 1,064 |
Ranking
ClinVar | |
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0 |
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0 |
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498 |
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1,640 |
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24 |
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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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 |
---|---|
SYNONYM | CLSS |
SYNONYM | CMS17 |
SYNONYM | LRP-4 |
SYNONYM | LRP10 |
SYNONYM | MEGF7 |
SYNONYM | SOST2 |
MIM | 604270 OMIM |
HGNC | HGNC:6696 HGNC |
Ensembl | ENSG00000134569 Ensembl |
AllianceGenome | HGNC:6696 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000378623.6 | hg38 | chr11 | 46,856,717 | 46,918,550 | 61,834 |
ENST00000378623.6 | hg19 | chr11 | 46,878,268 | 46,940,101 | 61,834 |
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