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See other PCCA CNV Assays ›
Gene Symbol
PCCA
Assay Reference Genome
Location

Chr.13:100391623 on build GRCh38
Cytoband
13q32.3
Assay ID Hs06388333_cn
Size
Availability Made To Order
Catalog # 4400291
Price
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Assay Details

Target Gene Details

Entrez Gene ID:

 5095

Gene Name:

 propionyl-CoA carboxylase alpha subunit

Gene Aliases:

 -

Location:

 Chr.13:100089015-100530437 on Build GRCh38

Assay Gene Location:

 Within Intron 25
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
PCCA NM_000282.3 NP_000273.2
NM_001127692.2 NP_001121164.1
NM_001178004.1 NP_001171475.1
XM_005254059.2 XP_005254116.1
XM_011521093.1 XP_011519395.1
XM_017020605.1 XP_016876094.1
XM_017020606.1 XP_016876095.1
XM_017020607.1 XP_016876096.1
XM_017020608.1 XP_016876097.1
XM_017020609.1 XP_016876098.1
XM_017020610.1 XP_016876099.1
XM_017020611.1 XP_016876100.1
XM_017020612.1 XP_016876101.1
XM_017020613.1 XP_016876102.1
XM_017020614.1 XP_016876103.1
XM_017020617.1 XP_016876106.1
XM_017020618.1 XP_016876107.1
AF385926.1 AAL66189.1
AK225288.1
AK225299.1
AK296771.1
AK298318.1
AK315503.1
BC000140.2 AAH00140.1
CB851764.1
S79219.1 AAB35181.1
X14608.1 CAA32763.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv1037571 Chr.13:100255653 - 100408741 on Build GRCh38 Loss PCCA
esv3892435 Chr.13:100324308 - 100420688 on Build GRCh38 Loss PCCA

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More Information


Additional Information:

For this assay, SNP(s) [rs149166067] 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

Panther Classification:

Molecular Function -

ligase

Gene Ontology Categories:

Function(s) Process(es)


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