Hs07002617_cn

• Gene Symbol: CLEC1B
• Assay Reference Genome Location: Chr.12:10000278 on build GRCh38
• Cytoband: 12p13.2

Target Gene Details

• Entrez Gene ID: 51266
• Gene Name: C-type lectin domain family 1 member B
• Gene Aliases: 1810061I13Rik, CLEC2, CLEC2B, PRO1384, QDED721
• Location: Chr.12:9986119-10001894 on Build GRCh38
• Assay Gene Location: Within Intron 2

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
CLEC1B	XM_005253382.4			XP_005253439.1
	XM_011520685.2			XP_011518987.1
	XM_017019395.1			XP_016874884.1
	BC029554.1			AAH29554.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
dgv1374n100	Chr.12:9968689 - 10026775 on Build GRCh38	Gain	CLEC12A CLEC1B LOC102724020 CLEC12B
nsv525593	Chr.12:9968748 - 10004047 on Build GRCh38	Loss	CLEC12A CLEC1B
nsv604	Chr.12:9991440 - 10007841 on Build GRCh38	Deletion	CLEC12A CLEC1B CLEC12B

More Information

Additional Information:

For this assay, SNP(s) [rs75265877] 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)

defense response
cell surface receptor signaling pathway
platelet activation
platelet formation

Function(s)

transmembrane signaling receptor activity
protein binding
carbohydrate binding