Hs06951995_cn

• Gene Symbol: TMEM132C
• Assay Reference Genome Location: Chr.12:128293201 on build GRCh38
• Cytoband: 12q24.32

Target Gene Details

• Entrez Gene ID: 92293
• Gene Name: transmembrane protein 132C
• Gene Aliases: PPP1R152
• Location: Chr.12:128267170-128707915 on Build GRCh38
• Assay Gene Location: Within Intron 2

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
TMEM132C	NM_001136103.2			NP_001129575.2
	XM_011538998.2			XP_011537300.1

Target Copy Number Variation Details

• DGV Version: Release date: 2016-05-15, GRCh GRCh38

Target Variation	Location	CNV Subtype	Genes
dgv1573n100	Chr.12:126502891 - 128427644 on Build GRCh38	Gain	LINC00943 LOC101927592 LINC00944 LOC101927694 LOC107984465 LINC00508 MIR3612 LOC101927616 LOC107984449 FLJ37505 LOC101927637 LINC00507 LOC105370068 LOC100996671 CRAT8 TMEM132C MIR4419B LOC100996679 LOC440117
nsv1160070	Chr.12:128223477 - 128299998 on Build GRCh38	Duplication	MIR3612 TMEM132C MIR4419B

More Information

Additional Information:

For this assay, SNP(s) [rs114289274] 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

Gene Ontology Categories:

Process(es)

biological_process

Function(s)

molecular_function