Hs03622819_cn

• Gene Symbol: C7orf49
• Assay Reference Genome Location: Chr.7:135151377 on build GRCh38
• Cytoband: 7q33

Target Gene Details

• Entrez Gene ID: 78996
• Gene Name: chromosome 7 open reading frame 49
• Gene Aliases: MRI
• Location: Chr.7:135092303-135170826 on Build GRCh38
• Assay Gene Location: Within Intron 5

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
C7orf49	NM_001305630.1			NP_001292559.1
	XM_017012595.1			XP_016868084.1

Target Gene Details

• Entrez Gene ID: 55281
• Gene Name: transmembrane protein 140
• Gene Aliases: -
• Location: Chr.7:135148014-135166215 on Build GRCh38
• Assay Gene Location: Within Intron 1

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
TMEM140	NM_018295.4			NP_060765.4
	AK001862.1			BAA91948.1
	AK225055.1
	AK301268.1
	BC020942.1			AAH20942.1
	DB064371.1
	DC323016.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv527174	Chr.7:134952791 - 135157183 on Build GRCh38	Loss	TMEM140 C7orf49 AGBL3 CALD1
nsv527014	Chr.7:135149118 - 135206907 on Build GRCh38	Gain	WDR91 TMEM140 C7orf49
esv3615115	Chr.7:135148990 - 135156413 on Build GRCh38	Loss	TMEM140 C7orf49
esv2665250	Chr.7:135149068 - 135156387 on Build GRCh38	Deletion	TMEM140 C7orf49

More Information

Additional Information:

For this assay, SNP(s) [rs73725242] 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