Assay Details
Target Gene Details
Entrez Gene ID: | 6575 |
Gene Name: | solute carrier family 20 member 2 |
Gene Aliases: |
GLVR-2, GLVR2, IBGC1, IBGC3, MLVAR, PIT-2, PIT2, RAM1, Ram-1 |
Location: |
Chr.8:42416462-42542213 on Build GRCh38 |
Assay Gene Location: | Within Intron 15 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
SLC20A2 | NM_001257180.1 | NP_001244109.1 | ||
NM_001257181.1 | NP_001244110.1 | |||
NM_006749.4 | NP_006740.1 | |||
XM_005273613.3 | XP_005273670.1 | |||
XM_005273615.3 | XP_005273672.1 | |||
XM_006716390.3 | XP_006716453.1 | |||
XM_006716391.3 | XP_006716454.1 | |||
XM_017013748.1 | XP_016869237.1 | |||
XM_017013749.1 | XP_016869238.1 | |||
XM_017013750.1 | XP_016869239.1 | |||
XM_017013751.1 | XP_016869240.1 | |||
XM_017013752.1 | XP_016869241.1 | |||
AK291202.1 | ||||
AK295952.1 | ||||
AK314774.1 | ||||
BC028600.2 | AAH28600.1 | |||
L20852.1 | AAA18018.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
esv3617010 | Chr.8:42419628 - 42426318 on Build GRCh38 | Loss |
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nsv831301 | Chr.8:42244080 - 42473666 on Build GRCh38 | Loss |
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More Information
Additional Information:
For this assay, SNP(s) [rs78582093] 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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