Assay Details
Target Gene Details
Entrez Gene ID: | 55536 |
Gene Name: | cell division cycle associated 7 like |
Gene Aliases: |
JPO2, R1, RAM2 |
Location: |
Chr.7:21900899-21945924 on Build GRCh38 |
Assay Gene Location: | Within Exon 11 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
CDCA7L | NM_001127370.2 | 11 | 2498 | NP_001120842.1 |
NM_001127371.2 | 9 | 2306 | NP_001120843.1 | |
NM_018719.4 | 10 | 2444 | NP_061189.2 | |
AK022955.1 | 11 | 1988 | BAB14330.1 | |
AK095965.1 | 11 | 2452 | ||
AL359619.1 | 5 | 1570 | CAB94887.1 | |
BC009352.2 | 10 | 2336 | AAH09352.2 | |
BC014630.2 | 9 | 2288 | AAH14630.2 | |
BC025242.1 | 10 | 2398 | AAH25242.1 | |
BC032576.1 | 10 | 2409 | AAH32576.1 | |
BC039823.1 | 10 | 2408 | AAH39823.1 | |
BU753973.1 |
Target Gene Details
Entrez Gene ID: | 8701 |
Gene Name: | dynein axonemal heavy chain 11 |
Gene Aliases: |
CILD7, DNAHBL, DNAHC11, DNHBL, DPL11 |
Location: |
Chr.7:21543215-21901568 on Build GRCh38 |
Assay Gene Location: | Within Exon 82 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
DNAH11 | NM_001277115.1 | 82 | 13691 | NP_001264044.1 |
AI743846.1 | 1 | 487 | ||
AJ320497.1 | CAC60121.1 | |||
AK054657.1 | 12 | 2134 | BAB70785.1 | |
AL529367.3 | 1 | 447 | ||
CA424782.1 | 1 | 493 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv830922 | Chr.7:21753768 - 21925057 on Build GRCh38 | Loss | CDCA7L DNAH11 |
nsv1027453 | Chr.7:21878856 - 21942830 on Build GRCh38 | Gain | CDCA7L DNAH11 |
More Information
Additional Information:
For this assay, SNP(s) [rs79947346] 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 |