Assay Details
Target Gene Details
Entrez Gene ID: | 57626 |
Gene Name: | kelch like family member 1 |
Gene Aliases: |
MRP2 |
Location: |
Chr.13:69700593-70108493 on Build GRCh38 |
Assay Gene Location: | Within Exon 13 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
KLHL1 | NM_001286725.1 | 10 | 3029 | NP_001273654.1 |
NM_020866.2 | 11 | 3212 | NP_065917.1 | |
XM_017020678.1 | 11 | 2132 | XP_016876167.1 | |
XM_017020679.1 | 11 | 2719 | XP_016876168.1 | |
AB040923.1 | 11 | 3178 | ||
AF252283.1 | 11 | 3046 | AAF81719.1 | |
AK291435.1 | 11 | 3212 | ||
BC022460.1 | 11 | 2456 | AAH22460.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv1045844 | Chr.13:69463964 - 69831303 on Build GRCh38 | Gain | KLHL1 |
nsv1049684 | Chr.13:69552739 - 69759313 on Build GRCh38 | Gain | KLHL1 |
nsv562207 | Chr.13:69623503 - 69714126 on Build GRCh38 | Loss | KLHL1 |
More Information
Additional Information:
For this assay, SNP(s) [rs74092454] 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 Exonic DGV Variation |