Hs02111327_cn

• Gene Symbol: PNISR
• Assay Reference Genome Location: Chr.6:99401396 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	1800	NP_001309334.1
	NM_001322406.1	13	1916	NP_001309335.1
	NM_001322408.1	11	1720	NP_001309337.1
	NM_001322410.1	12	1804	NP_001309339.1
	NM_001322412.1	12	1800	NP_001309341.1
	NM_001322413.1	11	1724	NP_001309342.1
	NM_001322414.1	11	1750	NP_001309343.1
	NM_001322415.1	10	1670	NP_001309344.1
	NM_001322416.1			NP_001309345.1
	NM_015491.2	11	1724	NP_056306.1
	NM_032870.3	12	1804	NP_116259.2
	NR_136326.1	10	2444
	XM_005266912.3	11	1683	XP_005266969.2
	XM_017010710.1	11	1747	XP_016866199.1
	XM_017010711.1	10	1633	XP_016866200.1
	XM_017010712.1	12	3155	XP_016866201.1
	XM_017010713.1	12	3151	XP_016866202.1
	AA626029.1
	AF314184.1	10	1594	AAL76163.1
	AF314185.1			AAL76164.1
	AJ420559.1	1	1043
	AK074628.1			BAC11098.1
	AL080186.1	1	45	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	PNISR COQ3
nsv527517	Chr.6:99394180 - 99416102 on Build GRCh38	Loss	PNISR COQ3
nsv1029536	Chr.6:98422726 - 99818247 on Build GRCh38	Loss	PNISR LOC101927365 MIR548AI FAXC FBXL4 CCNC USP45 TSTD3 PRDM13 POU3F2 COQ3

More Information

• Set Membership: Intragenic, Exonic, DGV Variation

Gene Ontology Categories:

Function(s)

poly(A) RNA binding