Hs05575892_cn

• Gene Symbol: PISD
• Assay Reference Genome Location: Chr.22:31629880 on build GRCh38
• Cytoband: 22q12.2

Target Gene Details

• Entrez Gene ID: 23761
• Gene Name: phosphatidylserine decarboxylase
• Gene Aliases: DJ858B16, PSD, PSDC, PSSC, dJ858B16.2
• Location: Chr.22:31618491-31630824 on Build GRCh38
• Assay Gene Location: Within Intron 6

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
PISD	NM_001326411.1			NP_001313340.1
	NM_001326412.1			NP_001313341.1
	NM_001326413.1			NP_001313342.1
	NM_001326414.1			NP_001313343.1
	NM_001326415.1			NP_001313344.1
	NM_001326416.1			NP_001313345.1
	NM_001326417.1			NP_001313346.1
	NM_001326418.1			NP_001313347.1
	NM_001326419.1			NP_001313348.1
	NM_001326420.1			NP_001313349.1
	NM_001326421.1			NP_001313350.1
	NM_014338.3			NP_055153.1
	NM_178022.1			NP_821141.1
	AK298474.1
	AL050371.1			CAB43678.2
	BC001482.2			AAH01482.1
	CR456540.1			CAG30426.1
	DQ655940.2
	DQ656048.2

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv829176	Chr.22:31602237 - 31633570 on Build GRCh38	Loss	SFI1 PISD MIR7109
nsv953070	Chr.22:31609915 - 31630414 on Build GRCh38	Deletion	SFI1 PISD MIR7109

More Information

Additional Information:

For this assay, SNP(s) [rs73881398] 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 -

decarboxylase

Gene Ontology Categories:

Process(es)

phosphatidylethanolamine biosynthetic process
protein autoprocessing

Function(s)

phosphatidylserine decarboxylase activity