Hs03367722_cn

• Gene Symbol: FAM213B
• Assay Reference Genome Location: Chr.1:2586537 on build GRCh38
• Cytoband: 1p36.32

Target Gene Details

• Entrez Gene ID: 127281
• Gene Name: family with sequence similarity 213 member B
• Gene Aliases: C1orf93
• Location: Chr.1:2586460-2591469 on Build GRCh38
• Assay Gene Location: Overlaps Exon 1 - Intron 1

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
FAM213B	NR_036637.1
	NR_036638.1
	BI908668.1
	DA292832.1
	DA495138.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv829648	Chr.1:2567689 - 2640901 on Build GRCh38	Loss	LOC100996583 FAM213B MMEL1 TTC34
esv3582248	Chr.1:2569899 - 2636548 on Build GRCh38	Gain	LOC100996583 FAM213B MMEL1
nsv545077	Chr.1:2428542 - 2622185 on Build GRCh38	Gain	LOC100996583 FAM213B MMEL1 PANK4 LOC115110 HES5 TNFRSF14 PLCH2
nsv545082	Chr.1:2536231 - 2597243 on Build GRCh38	Loss	LOC100996583 FAM213B MMEL1 LOC115110 TNFRSF14
nsv470684	Chr.1:2394570 - 2930923 on Build GRCh38	Loss	LOC100996583 FAM213B MMEL1 RER1 PANK4 PEX10 LOC115110 HES5 TNFRSF14 PLCH2 TTC34
nsv545083	Chr.1:2575976 - 2653099 on Build GRCh38	Gain	LOC100996583 FAM213B MMEL1 TTC34
nsv951592	Chr.1:2564862 - 2613961 on Build GRCh38	Deletion	LOC100996583 FAM213B MMEL1 TNFRSF14

More Information

Additional Information:

For this assay, SNP(s) [rs111285510] 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, Non-exonic, DGV Variation

Gene Ontology Categories:

Process(es)

prostaglandin biosynthetic process
oxidation-reduction process

Function(s)

oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
prostaglandin-F synthase activity