Hs05718503_cn

• Gene Symbol: RBP7
• Assay Reference Genome Location: Chr.1:9999696 on build GRCh38
• Cytoband: 1p36.22

Target Gene Details

• Entrez Gene ID: 116362
• Gene Name: retinol binding protein 7
• Gene Aliases: CRBP4, CRBPIV
• Location: Chr.1:9997197-10016020 on Build GRCh38
• Assay Gene Location: Within Intron 1

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
RBP7	NM_052960.2			NP_443192.1
	AF399927.1			AAK85409.1
	AK312027.1
	AY145438.1			AAN61071.1
	BC033883.1			AAH33883.1
	BC063013.1			AAH63013.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
esv3585192	Chr.1:9992655 - 10003176 on Build GRCh38	Loss	RBP7 NMNAT1
esv2667343	Chr.1:9992637 - 10003207 on Build GRCh38	Deletion	RBP7 NMNAT1
nsv1001742	Chr.1:9911718 - 10056709 on Build GRCh38	Gain	RBP7 NMNAT1 LZIC UBE4B MIR5697

More Information

Additional Information:

For this assay, SNP(s) [rs113346921] 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:

Process(es)

transport

Function(s)

transporter activity
protein binding
retinal binding
retinol binding