Hs04075394_cn

• Gene Symbol: FAM207A
• Assay Reference Genome Location: Chr.21:44939855 on build GRCh38
• Cytoband: 21q22.3

Target Gene Details

• Entrez Gene ID: 85395
• Gene Name: family with sequence similarity 207 member A
• Gene Aliases: C21orf70, PRED56
• Location: Chr.21:44939697-44976989 on Build GRCh38
• Assay Gene Location: Overlaps Exon 1 - Intron 1

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
FAM207A	NM_001316988.1			NP_001303917.1
	BG744869.1

Target Gene Details

• Entrez Gene ID: 84536
• Gene Name: long intergenic non-protein coding RNA 1547
• Gene Aliases: C21orf67, C21orf69, PRED54
• Location: Chr.21:44933284-44939913 on Build GRCh38
• Assay Gene Location: Within Exon 1

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
LINC01547	NR_027128.1	1	59
	NR_027129.1	1	59
	AF380178.1			AAL34496.1
	AK127059.1	1	59
	AY040088.1			AAK74136.1
	BI829356.1
	BI907880.1	1	59

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
esv3647138	Chr.21:44916487 - 44942284 on Build GRCh38	Loss	FAM207A ITGB2-AS1 LINC01547 ITGB2
nsv834110	Chr.21:44896268 - 45085236 on Build GRCh38	Loss	LINC00163 FAM207A LOC105372836 ITGB2-AS1 ADARB1 PICSAR LINC01547 ITGB2 SSR4P1

More Information

Additional Information:

For this assay, SNP(s) [rs76091017] 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, Exonic, Non-exonic, DGV Variation

Gene Ontology Categories:

Function(s)

protein binding