KLK11 kallikrein related peptidase 11
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 4 |
Likely benign | 0 | 6 |
Uncertain significance | 0 | 30 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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36 |
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4 |
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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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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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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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 | IEKD |
SYNONYM | PRSS20 |
SYNONYM | TLSP |
MIM | 604434 OMIM |
HGNC | HGNC:6359 HGNC |
Ensembl | ENSG00000167757 Ensembl |
AllianceGenome | HGNC:6359 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000600362.5 | hg38 | chr19 | 51,022,216 | 51,026,602 | 4,387 |
ENST00000319720.11 | hg38 | chr19 | 51,022,231 | 51,028,039 | 5,809 |
ENST00000391804.7 | hg38 | chr19 | 51,022,489 | 51,027,954 | 5,466 |
ENST00000453757.8 | hg38 | chr19 | 51,022,236 | 51,026,616 | 4,381 |
ENST00000594768.5 | hg38 | chr19 | 51,022,233 | 51,027,703 | 5,471 |
ENST00000600362.5 | hg19 | chr19 | 51,525,472 | 51,529,858 | 4,387 |
ENST00000319720.11 | hg19 | chr19 | 51,525,487 | 51,531,295 | 5,809 |
ENST00000594768.5 | hg19 | chr19 | 51,525,489 | 51,530,959 | 5,471 |
ENST00000453757.8 | hg19 | chr19 | 51,525,492 | 51,529,872 | 4,381 |
ENST00000391804.7 | hg19 | chr19 | 51,525,745 | 51,531,210 | 5,466 |
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