Hs04631689_cn

• Gene Symbol: GULP1
• Assay Reference Genome Location: Chr.2:188298132 on build GRCh38
• Cytoband: 2q32.1

Target Gene Details

• Entrez Gene ID: 51454
• Gene Name: GULP, engulfment adaptor PTB domain containing 1
• Gene Aliases: CED-6, CED6, GULP
• Location: Chr.2:188291669-188595926 on Build GRCh38
• Assay Gene Location: Within Intron 3

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
GULP1	NM_001252668.1			NP_001239597.1
	NM_001252669.1			NP_001239598.1
	NM_016315.3			NP_057399.1
	NR_045562.1
	NR_045563.1
	XM_006712580.3			XP_006712643.1
	XM_006712581.1			XP_006712644.1
	XM_006712582.1			XP_006712645.1
	XM_006712583.3			XP_006712646.1
	XM_006712584.3			XP_006712647.1
	XM_006712589.3			XP_006712652.1
	XM_011511329.1			XP_011509631.1
	XM_011511332.1			XP_011509634.1
	XM_011511333.1			XP_011509635.1
	XM_011511335.2			XP_011509637.1
	XM_017004303.1			XP_016859792.1
	XM_017004304.1			XP_016859793.1
	XM_017004305.1			XP_016859794.1
	XM_017004306.1			XP_016859795.1
	XM_017004307.1			XP_016859796.1
	XM_017004308.1			XP_016859797.1
	AF075014.1
	AF191771.1			AAF18975.1
	AF200715.1			AAF08006.1
	AK023668.1
	AK055718.1
	AK298626.1
	AK314498.1
	BC001103.2			AAH01103.1
	DA392794.1

More Information

Additional Information:

For this assay, SNP(s) [rs72905578] 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, non-DGV Variation

Panther Classification:

Molecular Function -

scaffold/adaptor protein

Gene Ontology Categories:

Process(es)

lipid transport
phagocytosis, engulfment
apoptotic process
signal transduction

Function(s)

signal transducer activity