Hs00636589_cn

• Gene Symbol: PNISR
• Assay Reference Genome Location: Chr.6:99406071 on build GRCh38
• Cytoband: 6q16.2

Target Gene Details

• Entrez Gene ID: 25957
• Gene Name: PNN interacting serine and arginine rich protein
• Gene Aliases: C6orf111, HSPC306, SFRS18, SRrp130, bA98I9.2
• Location: Chr.6:99398051-99425345 on Build GRCh38
• Assay Gene Location: Overlaps Intron 9 - Exon 9

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
PNISR	NM_001322405.1			NP_001309334.1
	NM_001322406.1			NP_001309335.1
	NM_001322408.1			NP_001309337.1
	NM_001322410.1			NP_001309339.1
	NM_001322412.1			NP_001309341.1
	NM_001322413.1			NP_001309342.1
	NM_001322414.1			NP_001309343.1
	NM_001322415.1			NP_001309344.1
	NM_001322416.1			NP_001309345.1
	NM_015491.2			NP_056306.1
	NM_032870.3			NP_116259.2
	NR_136326.1
	XM_005266912.3			XP_005266969.2
	XM_017010710.1			XP_016866199.1
	XM_017010711.1			XP_016866200.1
	XM_017010712.1			XP_016866201.1
	XM_017010713.1			XP_016866202.1
	AF161424.1			AAF28984.1
	AF314184.1			AAL76163.1
	AF314186.1			AAL76165.1
	AK027658.1			BAB55273.1
	AK027898.1			BAB55440.1
	AK074628.1			BAC11098.1
	AK291155.1
	AW081113.1
	BC012780.2			AAH12780.1
	BC064413.1			AAH64413.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
esv3890914	Chr.6:99393043 - 99409897 on Build GRCh38	Loss	PNISR COQ3
nsv527517	Chr.6:99394180 - 99416102 on Build GRCh38	Loss	PNISR COQ3
nsv1029536	Chr.6:98422726 - 99818247 on Build GRCh38	Loss	POU3F2 LOC101927365 CCNC FAXC FBXL4 PNISR TSTD3 USP45 COQ3 MIR548AI PRDM13

More Information

• Set Membership: Intragenic, Non-exonic, DGV Variation

Gene Ontology Categories:

Function(s)

poly(A) RNA binding