Assay Details
Target Gene Details
Entrez Gene ID: | 25874 |
Gene Name: | mitochondrial pyruvate carrier 2 |
Gene Aliases: |
BRP44 |
Location: |
Chr.1:167916675-167937069 on Build GRCh38 |
Assay Gene Location: | Within Intron 3 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
MPC2 | NM_001143674.3 | NP_001137146.1 | ||
NM_015415.3 | NP_056230.1 | |||
NR_026550.2 | ||||
XM_006711266.3 | XP_006711329.1 | |||
AK290126.1 | ||||
AK307189.1 | ||||
AK311913.1 | ||||
AL035304.1 | CAA22909.1 | |||
AL110297.1 | CAB53738.1 | |||
AL554033.3 | ||||
BC104157.1 | AAI04158.1 | |||
BC104158.1 | AAI04159.1 | |||
CR407632.1 | CAG28560.1 | |||
CR533473.1 | CAG38504.1 | |||
DC374001.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
esv32660 | Chr.1:167825845 - 168220986 on Build GRCh38 | Loss | MIR1255B2 TIPRL ADCY10 MPC2 GPR161 DCAF6 |
More Information
Additional Information:
For this assay, SNP(s) [rs114445667] 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 |