Genomic Map
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Target Gene Details
Entrez Gene ID: | 6528 |
Gene Name: | solute carrier family 5 member 5 |
Gene Aliases: |
NIS, TDH1 |
Location: |
Chr.19:17871394-17895175 on Build GRCh38 |
Assay Gene Location: | Within Exon 2 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| SLC5A5 | NM_000453.2 | NP_000444.1 | ||
| XM_011528192.2 | XP_011526494.1 | |||
| XM_011528193.2 | XP_011526495.1 | |||
| XM_011528194.2 | 1 | 76 | XP_011526496.1 | |
| XM_017027158.1 | XP_016882647.1 | |||
| BC105047.1 | AAI05048.1 | |||
| BC105049.1 | AAI05050.1 | |||
| BX648217.1 | ||||
| D87920.1 | BAA24835.1 | |||
| U66088.1 | AAB17378.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv833772 | Chr.19:17854364 - 18028528 on Build GRCh38 | Gain+Loss |
 SLC5A5
RPL18A
KCNN1
CCDC124
SNORA68
ARRDC2
|
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Additional Information:
For this assay, SNP(s) [rs115249627] 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
Exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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