Hs02268786_cn

• Gene Symbol: P4HA2
• Assay Reference Genome Location: Chr.5:132192956 on build GRCh38
• Cytoband: 5q31.1

Target Gene Details

• Entrez Gene ID: 8974
• Gene Name: prolyl 4-hydroxylase subunit alpha 2
• Gene Aliases: -
• Location: Chr.5:132190147-132227863 on Build GRCh38
• Assay Gene Location: Within Exon 18

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
P4HA2	NM_001017973.1	15	2220	NP_001017973.1
	NM_001017974.1	15	1748	NP_001017974.1
	NM_001142598.1	16	1884	NP_001136070.1
	NM_001142599.1	16	1890	NP_001136071.1
	NM_004199.2	15	2226	NP_004190.1
	XM_005272116.4	15	1754	XP_005272173.1
	XM_005272117.4	16	1912	XP_005272174.1
	XM_005272118.4	16	2041	XP_005272175.1
	XM_005272119.4	16	2231	XP_005272176.1
	XM_005272120.4	16	2011	XP_005272177.1
	XM_006714728.3	16	2288	XP_006714791.1
	XM_006714729.3	16	1906	XP_006714792.1
	XM_006714730.3	16	2282	XP_006714793.1
	XM_011543705.2	13	1503	XP_011542007.1
	XM_017010011.1	16	2005	XP_016865500.1
	XM_017010012.1	14	1571	XP_016865501.1
	AY358970.1	15	1822	AAQ89329.1
	BC017062.1	15	1849
	BC035813.1	15	1717	AAH35813.1
	BX647924.1	15	1740	CAI46066.1
	U90441.1	15	1849	AAB71339.1

More Information

Additional Information:

For this assay, SNP(s) [rs71810391] 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 -

protein modifying enzyme

Gene Ontology Categories:

Process(es)

peptidyl-proline hydroxylation
oxidation-reduction process

Function(s)

procollagen-proline 4-dioxygenase activity
iron ion binding
electron carrier activity
oxidoreductase activity, acting on single donors with incorporation of molecular oxygen, incorporation of two atoms of oxygen
L-ascorbic acid binding