Hs06560667_cn

• Gene Symbol: FAM131C
• Assay Reference Genome Location: Chr.1:16069447 on build GRCh38
• Cytoband: 1p36.13

Target Gene Details

• Entrez Gene ID: 348487
• Gene Name: family with sequence similarity 131 member C
• Gene Aliases: C1orf117
• Location: Chr.1:16057769-16073632 on Build GRCh38
• Assay Gene Location: Within Intron 1

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
FAM131C	NM_182623.2			NP_872429.2
	AK094085.1			BAC04282.1
	AL529663.3
	BC016848.1			AAH16848.1
	BC037394.1			AAH37394.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv520148	Chr.1:16005414 - 16139508 on Build GRCh38	Loss	EPHA2 CLCNKB C1orf64 CLCNKA HSPB7 FAM131C
nsv829570	Chr.1:16032866 - 16077137 on Build GRCh38	Gain	CLCNKB CLCNKA FAM131C
nsv508936	Chr.1:15915852 - 16181025 on Build GRCh38	Insertion	SPEN EPHA2 CLCNKB C1orf64 CLCNKA HSPB7 FAM131C ZBTB17
nsv833758	Chr.1:15969028 - 16140519 on Build GRCh38	Gain+Loss	EPHA2 CLCNKB C1orf64 CLCNKA HSPB7 FAM131C ZBTB17
nsv954844	Chr.1:16013606 - 16077905 on Build GRCh38	Deletion	CLCNKB CLCNKA HSPB7 FAM131C
nsv470698	Chr.1:16013965 - 16070311 on Build GRCh38	Loss	CLCNKB CLCNKA HSPB7 FAM131C
nsv997887	Chr.1:15994515 - 16115208 on Build GRCh38	Gain	CLCNKB C1orf64 CLCNKA HSPB7 FAM131C

More Information

Additional Information:

For this assay, SNP(s) [rs141455783] 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