Hs03565306_cn

• Gene Symbol: C5orf45
• Assay Reference Genome Location: Chr.5:179858147 on build GRCh38
• Cytoband: 5q35.3

Target Gene Details

• Entrez Gene ID: 51149
• Gene Name: chromosome 5 open reading frame 45
• Gene Aliases: -
• Location: Chr.5:179837266-179858840 on Build GRCh38
• Assay Gene Location: Within Intron 1

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
C5orf45	NM_001017987.2			NP_001017987.1
	NM_016175.3			NP_057259.2
	AK293901.1
	AK295104.1
	AK298954.1
	BC069051.1			AAH69051.1
	BF965313.1
	BQ642639.1
	BX537968.1			CAD97932.1
	BX647375.1
	CN363239.1
	CR936785.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv469579	Chr.5:179757830 - 179933191 on Build GRCh38	Loss	RNF130 TBC1D9B C5orf45 MAML1 LOC100996419 LTC4S SQSTM1 MGAT4B MIR1229
esv3607755	Chr.5:179853436 - 179869950 on Build GRCh38	Loss	TBC1D9B C5orf45 LOC100996419

More Information

Additional Information:

For this assay, SNP(s) [rs74588210] 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)

biological_process

Function(s)

molecular_function