Hs02936748_cn

• Gene Symbol: HCCS
• Assay Reference Genome Location: Chr.X:11122917 on build GRCh38
• Cytoband: Xp22.2

Target Gene Details

• Entrez Gene ID: 3052
• Gene Name: holocytochrome c synthase
• Gene Aliases: CCHL, LSDMCA1, MCOPS7, MLS
• Location: Chr.X:11111286-11123086 on Build GRCh38
• Assay Gene Location: Within Exon 7

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
HCCS	NM_001122608.2	7	2131	NP_001116080.1
	NM_001171991.2	7	2094	NP_001165462.1
	NM_005333.4	7	2189	NP_005324.3
	AI027533.1	1	177
	AK097815.1	7	2116
	BC095455.1	7	2132	AAH95455.1
	CR749578.1	7	2146	CAH18370.1

More Information

Additional Information:

For this assay, SNP(s) [rs764569516] 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

Panther Classification:

Molecular Function -

lyase, metabolite interconversion enzyme

Gene Ontology Categories:

Process(es)

organ morphogenesis
oxidation-reduction process

Function(s)

holocytochrome-c synthase activity
metal ion binding