Hs05715775_cn

• Gene Symbol: SAMD13
• Assay Reference Genome Location: Chr.1:84346912 on build GRCh38
• Cytoband: 1p31.1

Target Gene Details

• Entrez Gene ID: 148418
• Gene Name: sterile alpha motif domain containing 13
• Gene Aliases: HSD-41, HSD-42
• Location: Chr.1:84298366-84350798 on Build GRCh38
• Assay Gene Location: Within Intron 6

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
SAMD13	NM_001010971.2			NP_001010971.1
	NM_001134663.1			NP_001128135.1
	NM_001134664.1			NP_001128136.1
	XM_017000377.1			XP_016855866.1
	AK056937.1
	AY604569.1			AAU14233.1
	AY604570.1			AAU14234.1
	DB459148.2

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv830426	Chr.1:84239241 - 84390546 on Build GRCh38	Gain	SAMD13 UOX LOC100128775
nsv830414	Chr.1:84171055 - 84358968 on Build GRCh38	Gain	PRKACB SAMD13 LOC100128775

More Information

Additional Information:

For this assay, SNP(s) [rs146976842] 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

Panther Classification:

Molecular Function -

chromatin/chromatin-binding, or -regulatory protein