Hs01925840_cn

• Gene Symbol: FAM129B
• Assay Reference Genome Location: Chr.9:127506486 on build GRCh38
• Cytoband: 9q34.11

Target Gene Details

• Entrez Gene ID: 64855
• Gene Name: family with sequence similarity 129 member B
• Gene Aliases: C9orf88, MEG-3, MINERVA, OC58, bA356B19.6
• Location: Chr.9:127505338-127579007 on Build GRCh38
• Assay Gene Location: Within Exon 17

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
FAM129B	NM_001035534.2	14	2631	NP_001030611.1
	NM_022833.3	14	2843	NP_073744.2
	XM_005252135.2	15	2690	XP_005252192.2
	XM_011518925.1	15	2862	XP_011517227.1
	AB210016.1	14	2581	BAE06098.1
	AF151783.1	14	2613	AAK57556.1
	AF192911.1	14	2834	AAQ13825.1
	AK023580.1	6	1642	BAB14615.1
	AK025804.1	2	999	BAB15240.1
	AK025951.1	1	435
	AL137555.1	13	2451	CAB70809.1
	BC001979.1	7	1730	AAH01979.2
	BC110345.1	5	1343	AAI10346.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv466569	Chr.9:127470144 - 127512011 on Build GRCh38	Loss	LRSAM1 FAM129B
nsv615368	Chr.9:127504287 - 127547894 on Build GRCh38	Loss	FAM129B

More Information

Additional Information:

For this assay, SNP(s) [rs199894907] 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)

negative regulation of apoptotic process
cell-cell adhesion

Function(s)

cadherin binding involved in cell-cell adhesion