Hs06538355_cn

• Gene Symbol: HNRNPR
• Assay Reference Genome Location: Chr.1:23331015 on build GRCh38
• Cytoband: 1p36.12

Target Gene Details

• Entrez Gene ID: 10236
• Gene Name: heterogeneous nuclear ribonucleoprotein R
• Gene Aliases: HNRPR, hnRNP-R
• Location: Chr.1:23304688-23344650 on Build GRCh38
• Assay Gene Location: Within Intron 5

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
HNRNPR	NM_001102397.2			NP_001095867.1
	NM_001102398.2			NP_001095868.1
	NM_001102399.2			NP_001095869.1
	NM_001297620.1			NP_001284549.1
	NM_001297621.1			NP_001284550.1
	NM_001297622.1			NP_001284551.1
	NM_005826.4			NP_005817.1
	XM_005245711.4			XP_005245768.1
	XM_011540471.2			XP_011538773.1
	XM_011540472.2			XP_011538774.1
	XM_011540474.2			XP_011538776.1
	XM_011540475.2			XP_011538777.1
	XM_011540476.2			XP_011538778.1
	XM_011540477.2			XP_011538779.1
	XM_017000008.1			XP_016855497.1
	XM_017000009.1			XP_016855498.1
	XM_017000010.1			XP_016855499.1
	AF000364.1			AAC39540.1
	AK297382.1
	AK297405.1
	AK300029.1
	AK311519.1
	AK313142.1
	AU126696.1
	BC001449.2			AAH01449.1
	BC110389.1
	BX640912.1			CAE45953.1
	BX647784.1
	DA496215.1
	DA773186.1
	DQ351905.1			ABC73063.1

More Information

Additional Information:

For this assay, SNP(s) [rs148332065] 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, non-DGV Variation

Panther Classification:

Molecular Function -

RNA metabolism protein

Gene Ontology Categories:

Process(es)

mRNA splicing, via spliceosome
mRNA processing
circadian rhythm
gene expression
negative regulation of catalytic activity
positive regulation of mRNA catabolic process
mRNA destabilization

Function(s)

nucleotide binding
RNA binding
mRNA 3'-UTR binding
protein binding
poly(A) RNA binding