Assay Details
Target Gene Details
Entrez Gene ID: | 285195 |
Gene Name: | solute carrier family 9 member A9 |
Gene Aliases: |
AUTS16, NHE9 |
Location: |
Chr.3:143265222-143848531 on Build GRCh38 |
Assay Gene Location: | Within Intron 18 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
SLC9A9 | NM_173653.3 | NP_775924.1 | ||
XM_011512703.2 | XP_011511005.1 | |||
XM_017006203.1 | XP_016861692.1 | |||
AB075486.1 | BAE45746.1 | |||
AB089794.1 | BAD69592.1 | |||
AK092932.1 | BAC04005.1 | |||
AK301816.1 | ||||
AK315107.1 | ||||
AL832304.1 | CAI46158.1 | |||
AY254100.1 | AAP80573.1 | |||
BC035779.1 | AAH35779.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
esv2759184 | Chr.3:143273855 - 143567137 on Build GRCh38 | Loss | SLC9A9 SLC9A9-AS1 |
More Information
Additional Information:
For this assay, SNP(s) [rs78178523] 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 Intronic Non-exonic DGV Variation |