Hs03464476_cn

• Gene Symbol: C3orf33
• Assay Reference Genome Location: Chr.3:155773439 on build GRCh38
• Cytoband: 3q25.31

Target Gene Details

• Entrez Gene ID: 285315
• Gene Name: chromosome 3 open reading frame 33
• Gene Aliases: AC3-33
• Location: Chr.3:155762612-155806287 on Build GRCh38
• Assay Gene Location: Within Intron 6

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
C3orf33	NM_001308229.1			NP_001295158.1
	NM_173657.2			NP_775928.1
	XM_005247379.4			XP_005247436.1
	XM_011512710.2			XP_011511012.1
	XM_011512711.2			XP_011511013.1
	AF115515.1			AAO06952.1
	AK055701.1			BAB70989.1
	AK289890.1
	AL832165.1
	BC042198.1			AAH42198.1
	BC064898.1			AAH64898.1
	DA275323.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv592081	Chr.3:155763308 - 155776126 on Build GRCh38	Gain	C3orf33
esv25006	Chr.3:155761458 - 155794985 on Build GRCh38	Gain	C3orf33
dgv1421e212	Chr.3:155766119 - 155774530 on Build GRCh38	Gain	C3orf33
nsv441844	Chr.3:155763307 - 155774388 on Build GRCh38	Gain	C3orf33
nsv592079	Chr.3:155757090 - 155776126 on Build GRCh38	Gain	C3orf33
esv3575619	Chr.3:155751288 - 155774530 on Build GRCh38	Gain	C3orf33
dgv4927n100	Chr.3:155758758 - 155774388 on Build GRCh38	Gain	C3orf33
esv3598284	Chr.3:155760377 - 155780857 on Build GRCh38	Loss	C3orf33
nsv1009618	Chr.3:155652245 - 155774388 on Build GRCh38	Gain	PLCH1 C3orf33
esv3598283	Chr.3:155759067 - 155869415 on Build GRCh38	Loss	SLC33A1 C3orf33
esv3893791	Chr.3:155763820 - 155776126 on Build GRCh38	Loss	C3orf33
nsv514997	Chr.3:155763277 - 155773949 on Build GRCh38	Loss	C3orf33
esv3575620	Chr.3:155757648 - 155796064 on Build GRCh38	Gain	C3orf33
esv33346	Chr.3:155763431 - 155780652 on Build GRCh38	Gain	C3orf33
nsv592080	Chr.3:155761433 - 155794055 on Build GRCh38	Gain	C3orf33
dgv4926n100	Chr.3:155757649 - 155797695 on Build GRCh38	Gain	C3orf33

More Information

Additional Information:

For this assay, SNP(s) [rs113198926] 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:

Process(es)

regulation of sequence-specific DNA binding transcription factor activity
negative regulation of ERK1 and ERK2 cascade