PRCP prolylcarboxypeptidase
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 4 |
not provided | 0 | 2 |
Uncertain significance | 0 | 48 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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52 |
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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
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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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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 | HUMPCP |
SYNONYM | PCP |
MIM | 176785 OMIM |
HGNC | HGNC:9344 HGNC |
Ensembl | ENSG00000137509 Ensembl |
AllianceGenome | HGNC:9344 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000393399.6 | hg38 | chr11 | 82,824,368 | 82,900,430 | 76,063 |
ENST00000679387.1 | hg38 | chr11 | 82,823,044 | 82,901,630 | 78,587 |
ENST00000680524.1 | hg38 | chr11 | 82,824,367 | 82,901,673 | 77,307 |
ENST00000681592.1 | hg38 | chr11 | 82,823,044 | 82,846,179 | 23,136 |
ENST00000313010.8 | hg38 | chr11 | 82,822,936 | 82,900,430 | 77,495 |
ENST00000679623.1 | hg38 | chr11 | 82,823,044 | 82,901,601 | 78,558 |
ENST00000681637.1 | hg38 | chr11 | 82,823,044 | 82,901,623 | 78,580 |
ENST00000680437.1 | hg38 | chr11 | 82,823,044 | 82,900,431 | 77,388 |
ENST00000680186.1 | hg38 | chr11 | 82,823,044 | 82,846,139 | 23,096 |
ENST00000531801.6 | hg38 | chr11 | 82,823,044 | 82,901,658 | 78,615 |
ENST00000680040.1 | hg38 | chr11 | 82,823,044 | 82,845,822 | 22,779 |
ENST00000680566.1 | hg38 | chr11 | 82,823,044 | 82,901,740 | 78,697 |
ENST00000681883.1 | hg38 | chr11 | 82,823,044 | 82,845,734 | 22,691 |
ENST00000681432.1 | hg38 | chr11 | 82,823,044 | 82,845,856 | 22,813 |
ENST00000534264.2 | hg38 | chr11 | 82,823,044 | 82,858,771 | 35,728 |
ENST00000679809.1 | hg38 | chr11 | 82,823,044 | 82,846,134 | 23,091 |
ENST00000532809.2 | hg38 | chr11 | 82,823,044 | 82,900,832 | 77,789 |
ENST00000313010.8 | hg19 | chr11 | 82,533,978 | 82,611,472 | 77,495 |
ENST00000393399.6 | hg19 | chr11 | 82,535,410 | 82,611,472 | 76,063 |
ENST00000531801.6 | hg19 | chr11 | 82,534,086 | 82,612,700 | 78,615 |
ENST00000532809.2 | hg19 | chr11 | 82,534,086 | 82,611,874 | 77,789 |
ENST00000679387.1 | hg19 | chr11 | 82,534,086 | 82,612,672 | 78,587 |
ENST00000679623.1 | hg19 | chr11 | 82,534,086 | 82,612,643 | 78,558 |
ENST00000680524.1 | hg19 | chr11 | 82,535,409 | 82,612,715 | 77,307 |
ENST00000680566.1 | hg19 | chr11 | 82,534,086 | 82,612,782 | 78,697 |
ENST00000680437.1 | hg19 | chr11 | 82,534,086 | 82,611,473 | 77,388 |
ENST00000534264.2 | hg19 | chr11 | 82,534,086 | 82,569,813 | 35,728 |
ENST00000679809.1 | hg19 | chr11 | 82,534,086 | 82,557,176 | 23,091 |
ENST00000680186.1 | hg19 | chr11 | 82,534,086 | 82,557,181 | 23,096 |
ENST00000680040.1 | hg19 | chr11 | 82,534,086 | 82,556,864 | 22,779 |
ENST00000681432.1 | hg19 | chr11 | 82,534,086 | 82,556,898 | 22,813 |
ENST00000681592.1 | hg19 | chr11 | 82,534,086 | 82,557,221 | 23,136 |
ENST00000681637.1 | hg19 | chr11 | 82,534,086 | 82,612,665 | 78,580 |
ENST00000681883.1 | hg19 | chr11 | 82,534,086 | 82,556,776 | 22,691 |
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