Hs05485429_cn

• Gene Symbol: CNTD1
• Assay Reference Genome Location: Chr.17:42805013 on build GRCh38
• Cytoband: 17q21.31

Target Gene Details

• Entrez Gene ID: 124817
• Gene Name: cyclin N-terminal domain containing 1
• Gene Aliases: CNTD
• Location: Chr.17:42798667-42811587 on Build GRCh38
• Assay Gene Location: Within Intron 4

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
CNTD1	NM_173478.2			NP_775749.2
	XM_005257043.4			XP_005257100.1
	XM_005257044.4			XP_005257101.1
	XM_005257045.4			XP_005257102.1
	XM_006721690.2			XP_006721753.1
	XM_011524310.2			XP_011522612.1
	XM_011524311.2			XP_011522613.1
	XM_017024171.1			XP_016879660.1
	AK097456.1			BAC05060.1
	AK302094.1
	BC026187.2			AAH26187.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv833450	Chr.17:42660985 - 42825144 on Build GRCh38	Loss	TUBG2 EZH1 VPS25 COA3 WNK4 CNTNAP1 CCR10 RAMP2 PLEKHH3 RAMP2-AS1 CNTD1 BECN1 MIR6781 MIR6780A

More Information

Additional Information:

For this assay, SNP(s) [rs575351771] 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)

reciprocal meiotic recombination
spermatogenesis