Genomic Map
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Target Gene Details
Entrez Gene ID: | 5650 |
Gene Name: | kallikrein related peptidase 7 |
Gene Aliases: |
PRSS6, SCCE, hK7 |
Location: |
Chr.19:50976479-50984064 on Build GRCh38 |
Assay Gene Location: | Within Intron 6 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| KLK7 | NM_001207053.1 | NP_001193982.1 | ||
| NM_001243126.1 | NP_001230055.1 | |||
| NM_005046.3 | NP_005037.1 | |||
| NM_139277.2 | NP_644806.1 | |||
| AF411214.1 | AAN03662.1 | |||
| AF411215.1 | AAN03663.1 | |||
| AK289660.1 | ||||
| AK295313.1 | ||||
| AY601109.1 | ||||
| AY646152.1 | AAT66047.1 | |||
| BC032005.1 | AAH32005.1 | |||
| DQ018784.1 | ||||
| KF963189.1 | ||||
| KF963190.1 | ||||
| KF963191.1 | ||||
| KF963192.1 | ||||
| KF963193.1 | ||||
| L33404.1 | AAC37551.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv1064207 | Chr.19:50971269 - 50994022 on Build GRCh38 | Loss |
 KLK7
|
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Additional Information:
For this assay, SNP(s) [rs77995531] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.
Set Membership: |
Intragenic
Intronic
Non-exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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