Genomic Map
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Target Gene Details
Entrez Gene ID: | 9368 |
Gene Name: | SLC9A3 regulator 1 |
Gene Aliases: |
EBP50, NHERF, NHERF-1, NHERF1, NPHLOP2 |
Location: |
Chr.17:74748612-74769360 on Build GRCh38 |
Assay Gene Location: | Within Intron 2 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| SLC9A3R1 | NM_004252.4 | NP_004243.1 | ||
| AF015926.1 | AAC52084.1 | |||
| AF036241.1 | AAC04572.1 | |||
| AK026581.1 | ||||
| AK094467.1 | ||||
| AK128474.1 | ||||
| AK312498.1 | ||||
| BC001443.2 | AAH01443.1 | |||
| BC003361.1 | AAH03361.1 | |||
| BC011777.1 | AAH11777.1 | |||
| BC049220.1 | AAH49220.1 | |||
| BC053350.1 | AAH53350.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv952367 | Chr.17:74751962 - 74961105 on Build GRCh38 | Deletion |
 SLC9A3R1
HID1
TMEM104
NAT9
OTOP2
FDXR
FADS6
USH1G
GRIN2C
OTOP3
|
| nsv523611 | Chr.17:74755524 - 74767659 on Build GRCh38 | Loss |
SLC9A3R1
|
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Additional Information:
For this assay, SNP(s) [rs73995843] 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
|
Gene Ontology Categories:
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