Hs00934740_cn

• Gene Symbol: CLN6
• Assay Reference Genome Location: Chr.15:68207082 on build GRCh38
• Cytoband: 15q23

Target Gene Details

• Entrez Gene ID: 54982
• Gene Name: ceroid-lipofuscinosis, neuronal 6, late infantile, variant
• Gene Aliases: CLN4A, HsT18960, nclf
• Location: Chr.15:68206992-68229742 on Build GRCh38
• Assay Gene Location: Within Exon 7

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
CLN6	NM_017882.2	7	2152	NP_060352.1
	AK000568.1	7	2097	BAA91260.1
	AK027604.1	7	2120	BAB55226.1
	AK074753.1	4	1646	BAC11181.1
	BC010849.1	7	2066	AAH10849.1
	BC013130.1	7	2003	AAH13130.1
	CA446197.1	1	107

More Information

Additional Information:

For this assay, SNP(s) [rs141489068] 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, non-DGV Variation

Gene Ontology Categories:

Process(es)

ganglioside metabolic process
lysosomal lumen acidification
visual perception
cholesterol metabolic process
protein catabolic process
glycosaminoglycan metabolic process
locomotion involved in locomotory behavior
cellular macromolecule catabolic process
positive regulation of proteolysis

Function(s)

protein binding
protein homodimerization activity