Assay Details
Target Gene Details
Entrez Gene ID: | 133308 |
Gene Name: | solute carrier family 9 member B2 |
Gene Aliases: |
NHA2, NHE10, NHEDC2 |
Location: |
Chr.4:103018033-103077371 on Build GRCh38 |
Assay Gene Location: | Within Exon 11 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
SLC9B2 | NM_001300754.1 | 9 | 1296 | NP_001287683.1 |
NM_001300756.1 | 9 | 1662 | NP_001287685.1 | |
NM_178833.5 | 10 | 1833 | NP_849155.2 | |
XM_006714085.2 | 10 | 1832 | XP_006714148.1 | |
XM_006714086.3 | 9 | 1661 | XP_006714149.1 | |
AK172823.1 | 10 | 1833 | BAD18790.1 | |
AK297010.1 | 9 | 1207 | ||
AK299888.1 | 9 | 1221 | ||
BC009732.1 | 7 | 901 | AAH09732.1 | |
BC047447.1 | 10 | 1363 | AAH47447.2 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv4445 | Chr.4:103003411 - 103034963 on Build GRCh38 | Insertion |
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nsv461598 | Chr.4:102886563 - 103032232 on Build GRCh38 | Loss |
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nsv830021 | Chr.4:103013297 - 103179431 on Build GRCh38 | Loss |
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esv2759270 | Chr.4:102859548 - 103136164 on Build GRCh38 | Gain |
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More Information
Additional Information:
For this assay, SNP(s) [rs72943528] 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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Gene Ontology Categories:
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