Assay Details
Target Gene Details
Entrez Gene ID: | 83394 |
Gene Name: | PITPNM family member 3 |
Gene Aliases: |
ACKR6, CORD5, NIR1, RDGBA3 |
Location: |
Chr.17:6451263-6556557 on Build GRCh38 |
Assay Gene Location: | Within Intron 21 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
PITPNM3 | NM_001165966.1 | NP_001159438.1 | ||
NM_031220.3 | NP_112497.2 | |||
AB209130.1 | BAD92367.1 | |||
AF334586.1 | AAK01446.1 | |||
AL389994.1 | CAB97544.1 | |||
BC128583.1 | ||||
BC128584.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv574278 | Chr.17:5546345 - 6722066 on Build GRCh38 | Gain |
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nsv952115 | Chr.17:6454781 - 6512380 on Build GRCh38 | Deletion |
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More Information
Additional Information:
For this assay, SNP(s) [rs73346333,rs75515296] 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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