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System Message

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Gene Symbol: PRMT7
Assay Reference Genome Location: Chr.16:68316060 on build GRCh38
Cytoband: 16q22.1

Assay ID

Hs02334972_cn

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Availability	Made To Order
Catalog #	4400291
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Genomic Map
Assay Details
More Information

Assay Details

Target Gene Details

Entrez Gene ID:	54496
Gene Name:	protein arginine methyltransferase 7
Gene Aliases:	-
Location:	Chr.16:68310974-68358832 on Build GRCh38
Assay Gene Location:	Overlaps Exon 4 - Intron 4

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
PRMT7	NM_001184824.1			NP_001171753.1
	NM_001290018.1			NP_001276947.1
	NM_019023.2			NP_061896.1
	XM_011523112.2			XP_011521414.1
	XM_011523113.2			XP_011521415.1
	XM_011523115.2			XP_011521417.1
	XM_011523116.2			XP_011521418.1
	XM_011523121.2			XP_011521423.1
	XM_011523124.2			XP_011521426.1
	XM_011523125.2			XP_011521427.1
	XM_011523126.2			XP_011521428.1
	XM_011523128.2			XP_011521430.1
	XM_011523131.2			XP_011521433.1
	XM_017023290.1			XP_016878779.1
	XM_017023291.1			XP_016878780.1
	XM_017023292.1			XP_016878781.1
	XM_017023293.1			XP_016878782.1
	XM_017023294.1			XP_016878783.1
	XM_017023295.1			XP_016878784.1
	XM_017023296.1			XP_016878785.1
	XM_017023297.1			XP_016878786.1
	XM_017023298.1			XP_016878787.1
	XM_017023299.1			XP_016878788.1
	XM_017023300.1			XP_016878789.1
	XM_017023301.1			XP_016878790.1
	XM_017023302.1			XP_016878791.1
	XM_017023303.1			XP_016878792.1
	XM_017023304.1			XP_016878793.1
	XM_017023305.1			XP_016878794.1
	XM_017023306.1			XP_016878795.1
	XM_017023307.1			XP_016878796.1
	XM_017023308.1			XP_016878797.1
	XM_017023309.1			XP_016878798.1
	XM_017023310.1			XP_016878799.1
	XM_017023311.1			XP_016878800.1
	XM_017023312.1			XP_016878801.1
	XM_017023313.1			XP_016878802.1
	XM_017023314.1			XP_016878803.1
	XM_017023315.1			XP_016878804.1
	XM_017023316.1			XP_016878805.1
	AK001502.1			BAA91726.1
	AK056647.1
	AK097175.1
	AK304605.1
	BC000146.1			AAH00146.1
	DA287041.1
	DA648148.1

Target Copy Number Variation Details

DGV Version:

Release date: 2016-05-15, GRCh GRCh38

Target Variation	Location	CNV Subtype	Genes
nsv510691	Chr.16:68266527 - 68325431 on Build GRCh38	Deletion	SLC7A6 SLC7A6OS PRMT7

More Information

Set Membership:

Intragenic

Non-exonic

DGV Variation

Panther Classification:

Molecular Function -

protein modifying enzyme

Gene Ontology Categories:

Function(s) Process(es)

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