Hs04721423_cn

• Gene Symbol: GOLGA4
• Assay Reference Genome Location: Chr.3:37264101 on build GRCh38
• Cytoband: 3p22.2

Target Gene Details

• Entrez Gene ID: 2803
• Gene Name: golgin A4
• Gene Aliases: CRPF46, GCP2, GOLG, MU-RMS-40.18, p230
• Location: Chr.3:37243191-37366879 on Build GRCh38
• Assay Gene Location: Within Intron 4

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
GOLGA4	NM_001172713.1			NP_001166184.1
	NM_002078.4			NP_002069.2
	XM_005265069.3			XP_005265126.1
	XM_005265070.3			XP_005265127.1
	XM_005265071.3			XP_005265128.1
	XM_005265072.3			XP_005265129.1
	XM_005265073.1			XP_005265130.1
	XM_005265074.1			XP_005265131.1
	XM_005265075.1			XP_005265132.1
	XM_006713110.2			XP_006713173.1
	XM_017006184.1			XP_016861673.1
	XM_017006185.1			XP_016861674.1
	XM_017006186.1			XP_016861675.1
	XM_017006187.1			XP_016861676.1
	XM_017006188.1			XP_016861677.1
	AB209693.1			BAD92930.1
	AK290550.1
	AK300192.1
	AK307429.1
	BC045543.1			AAH45543.1
	BC050444.1			AAH50444.1
	U41740.1			AAC50434.1
	X82834.1			CAA58041.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv834665	Chr.3:37180973 - 37368088 on Build GRCh38	Loss	GOLGA4 LOC152048

More Information

Additional Information:

For this assay, SNP(s) [rs79735684] 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

Panther Classification:

Molecular Function -

membrane traffic protein, membrane trafficking regulatory protein

Gene Ontology Categories:

Process(es)

protein targeting to Golgi
vesicle-mediated transport
Golgi to plasma membrane protein transport
positive regulation of axon extension

Function(s)

protein binding
GTPase binding