Hs00908114_cn

• Gene Symbol: RNF219
• Assay Reference Genome Location: Chr.13:78614298 on build GRCh38
• Cytoband: 13q31.1

Target Gene Details

• Entrez Gene ID: 79596
• Gene Name: ring finger protein 219
• Gene Aliases: C13orf7
• Location: Chr.13:78614286-78659179 on Build GRCh38
• Assay Gene Location: Overlaps - Exon 6

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
RNF219	NM_024546.3			NP_078822.3
	XM_011535225.1			XP_011533527.1
	XM_017020743.1			XP_016876232.1
	AK023511.1			BAB14594.1
	AL136651.1			CAB66586.3
	BM674566.1
	CR936752.1
	CR936754.1
	CR936764.1

Target Gene Details

• Entrez Gene ID: 100874222
• Gene Name: RNF219 antisense RNA 1
• Gene Aliases: POU4F1-AS1
• Location: Chr.13:78054855-78617325 on Build GRCh38
• Assay Gene Location: Within Intron 5

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
RNF219-AS1	NR_047001.1
	AK095779.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
dgv339n67	Chr.13:78560929 - 78651758 on Build GRCh38	Gain	RNF219-AS1 RNF219 POU4F1 LOC107987188
dgv234n27	Chr.13:78566708 - 78642283 on Build GRCh38	Loss	RNF219-AS1 RNF219 POU4F1 LOC107987188

More Information

Additional Information:

For this assay, SNP(s) [rs76294763] 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, DGV Variation

Gene Ontology Categories:

Function(s)

protein binding
zinc ion binding