Assay Details
Target Gene Details
Entrez Gene ID: | 27013 |
Gene Name: | cyclin Pas1/PHO80 domain containing 1 |
Gene Aliases: |
C2orf24, CGI-57 |
Location: |
Chr.2:219171897-219178174 on Build GRCh38 |
Assay Gene Location: | Within Exon 11 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
CNPPD1 | NM_001321389.1 | 9 | 2187 | NP_001308318.1 |
NM_001321390.1 | 9 | 1832 | NP_001308319.1 | |
NM_001321391.1 | 9 | 1866 | NP_001308320.1 | |
NM_015680.5 | 8 | 1924 | NP_056495.3 | |
NR_135628.1 | 8 | 1804 | ||
NR_135629.1 | 7 | 1862 | ||
AF070638.1 | 2 | 1186 | AAC25393.1 | |
AK075274.1 | 8 | 1880 | ||
AY007160.1 | 8 | 1897 | AAG02008.1 | |
BC001393.2 | 8 | 1847 | AAH01393.1 | |
BC012821.2 | 8 | 1896 | AAH12821.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv508200 | Chr.2:219134744 - 219202175 on Build GRCh38 | Deletion | SLC23A3 FAM134A CNPPD1 NHEJ1 |
More Information
Additional Information:
For this assay, SNP(s) [rs73993507] 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 |