Hs01694987_cn

• Gene Symbol: PNISR
• Assay Reference Genome Location: Chr.6:99401063 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: Within Exon 12

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
PNISR	NM_001322405.1	12	2133	NP_001309334.1
	NM_001322406.1	13	2249	NP_001309335.1
	NM_001322408.1	11	2053	NP_001309337.1
	NM_001322410.1	12	2137	NP_001309339.1
	NM_001322412.1	12	2133	NP_001309341.1
	NM_001322413.1	11	2057	NP_001309342.1
	NM_001322414.1	11	2083	NP_001309343.1
	NM_001322415.1	10	2003	NP_001309344.1
	NM_001322416.1			NP_001309345.1
	NM_015491.2	11	2057	NP_056306.1
	NM_032870.3	12	2137	NP_116259.2
	NR_136326.1	10	2777
	XM_005266912.3	11	2016	XP_005266969.2
	XM_017010710.1	11	2080	XP_016866199.1
	XM_017010711.1	10	1966	XP_016866200.1
	XM_017010712.1	12	3488	XP_016866201.1
	XM_017010713.1	12	3484	XP_016866202.1
	AA626029.1
	AF314184.1	10	1927	AAL76163.1
	AF314185.1	1	329	AAL76164.1
	AJ420559.1	1	1376
	AL080186.1	1	378	CAB45767.1

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	COQ3 PNISR
nsv527517	Chr.6:99394180 - 99416102 on Build GRCh38	Loss	COQ3 PNISR
nsv1029536	Chr.6:98422726 - 99818247 on Build GRCh38	Loss	USP45 CCNC POU3F2 LOC101927365 MIR548AI FAXC FBXL4 COQ3 PNISR TSTD3 PRDM13

More Information

• Set Membership: Intragenic, Exonic, DGV Variation

Gene Ontology Categories:

Function(s)

poly(A) RNA binding