Hs00674304_cn

• Gene Symbol: FAM131B
• Assay Reference Genome Location: Chr.7:143355863 on build GRCh38
• Cytoband: 7q34

Target Gene Details

• Entrez Gene ID: 9715
• Gene Name: family with sequence similarity 131 member B
• Gene Aliases: -
• Location: Chr.7:143353400-143382304 on Build GRCh38
• Assay Gene Location: Within Exon 9

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
FAM131B	NM_001031690.2	7	1914	NP_001026860.2
	NM_001278297.1	6	1820	NP_001265226.1
	NM_014690.4	7	1807	NP_055505.3
	XM_005250073.3	7	2128	XP_005250130.1
	XM_006716186.2	7	1906	XP_006716249.1
	AB018316.1	6	1702
	AK124557.1	7	1862
	AL832579.2	6	3395	CAD89938.1
	BC045611.1	7	1919	AAH45611.2
	BC050543.1	7	1782

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv949966	Chr.7:143351408 - 143357207 on Build GRCh38	Deletion	CLCN1 FAM131B
nsv517520	Chr.7:143352880 - 143400007 on Build GRCh38	Loss	MIR6892 ZYX LOC100507507 FAM131B EPHA1

More Information

Additional Information:

For this assay, SNP(s) [rs111842640] 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, DGV Variation

Gene Ontology Categories:

Process(es)

positive regulation of defense response to virus by host
mitophagy in response to mitochondrial depolarization
xenophagy

Function(s)

protein binding