Assay Details
Target Gene Details
Entrez Gene ID: | 92211 |
Gene Name: | cadherin related family member 1 |
Gene Aliases: |
CORD15, PCDH21, PRCAD, RP65 |
Location: |
Chr.10:84194635-84219621 on Build GRCh38 |
Assay Gene Location: | Within Intron 9 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
CDHR1 | NM_001171971.2 | NP_001165442.1 | ||
NM_033100.3 | NP_149091.1 | |||
XM_011540337.1 | XP_011538639.1 | |||
XM_011540338.1 | XP_011538640.1 | |||
XM_011540339.1 | XP_011538641.1 | |||
XM_011540340.2 | XP_011538642.1 | |||
AB053448.1 | BAB61905.1 | |||
AB593154.1 | ||||
AB593155.1 | ||||
AK124752.1 | ||||
BC038799.1 | AAH38799.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv1046749 | Chr.10:83270389 - 84629720 on Build GRCh38 | Gain |
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nsv551753 | Chr.10:84187538 - 84215514 on Build GRCh38 | Loss |
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nsv551745 | Chr.10:83260366 - 84632635 on Build GRCh38 | Gain |
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More Information
Additional Information:
For this assay, SNP(s) [rs117206971] 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: |
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Panther Classification:
Gene Ontology Categories:
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