Assay Details
Target Gene Details
Entrez Gene ID: | 101928212 |
Gene Name: | uncharacterized LOC101928212 |
Gene Aliases: |
- |
Location: |
Chr.21:42569024-42573810 on Build GRCh38 |
Assay Gene Location: | Within Exon 2 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
LOC101928212 | XM_017028524.1 | 2 | 3299 | XP_016884013.1 |
XM_017028525.1 | 1 | 1960 | XP_016884014.1 |
Target Gene Details
Entrez Gene ID: | 54020 |
Gene Name: | solute carrier family 37 member 1 |
Gene Aliases: |
G3PP |
Location: |
Chr.21:42499632-42581440 on Build GRCh38 |
Assay Gene Location: | Within Intron 21 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
SLC37A1 | NM_001320537.1 | NP_001307466.1 | ||
NM_018964.3 | NP_061837.3 | |||
XM_011529614.2 | XP_011527916.1 | |||
XM_011529615.1 | XP_011527917.1 | |||
XM_017028376.1 | XP_016883865.1 | |||
XM_017028377.1 | XP_016883866.1 | |||
XM_017028378.1 | XP_016883867.1 | |||
XM_017028379.1 | XP_016883868.1 | |||
XM_017028380.1 | XP_016883869.1 | |||
XM_017028381.1 | XP_016883870.1 | |||
XM_017028382.1 | XP_016883871.1 | |||
AF311320.1 | AAG29853.1 | |||
AJ269529.2 | CAB87248.1 | |||
AK025993.1 | ||||
BM550728.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv522001 | Chr.21:42421796 - 42827928 on Build GRCh38 | Gain | PDE9A LOC101928255 RSPH1 LOC101928311 LOC101928233 LOC101928212 UBASH3A LOC101930094 LOC101928284 SLC37A1 |
nsv3533 | Chr.21:42563085 - 42603046 on Build GRCh38 | Deletion | LOC101928233 LOC101928212 SLC37A1 |
esv4794 | Chr.21:42569933 - 42570436 on Build GRCh38 | Loss | LOC101928212 SLC37A1 |
esv2723556 | Chr.21:42569770 - 42570443 on Build GRCh38 | Deletion | LOC101928212 SLC37A1 |
nsv834103 | Chr.21:42456611 - 42612638 on Build GRCh38 | Gain | RSPH1 LOC101928233 LOC101928212 LOC101930094 SLC37A1 |
nsv587633 | Chr.21:42485217 - 42631745 on Build GRCh38 | Gain | RSPH1 LOC101928233 LOC101928212 LOC101930094 SLC37A1 |
More Information
Additional Information:
For this assay, SNP(s) [rs73375843] 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 Intronic Non-exonic DGV Variation |