Hs02982057_cn

• Gene Symbol: PHF21A
• Assay Reference Genome Location: Chr.11:45932809 on build GRCh38
• Cytoband: 11p11.2

Target Gene Details

• Entrez Gene ID: 51317
• Gene Name: PHD finger protein 21A
• Gene Aliases: BHC80, BM-006
• Location: Chr.11:45929319-46121434 on Build GRCh38
• Assay Gene Location: Within Exon 27

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
PHF21A	NM_001101802.1	18	3826	NP_001095272.1
	NM_016621.3	18	3688	NP_057705.3
	XM_005252965.4	19	3518	XP_005253022.1
	XM_011520157.2	18	3379	XP_011518459.1
	XM_011520158.2	19	3731	XP_011518460.1
	XM_011520160.2	21	3892	XP_011518462.1
	XM_011520161.2	21	3983	XP_011518463.1
	XM_011520162.2	21	3861	XP_011518464.1
	XM_011520164.2	20	3790	XP_011518466.1
	XM_011520165.2	20	3745	XP_011518467.1
	XM_011520166.2	20	3668	XP_011518468.1
	XM_011520167.2	20	3871	XP_011518469.1
	XM_011520168.2	20	3723	XP_011518470.1
	XM_011520169.2	19	3682	XP_011518471.1
	XM_011520173.2	19	3638	XP_011518475.1
	XM_011520174.2	20	3612	XP_011518476.1
	XM_011520175.2	20	3609	XP_011518477.1
	XM_011520179.2	19	3491	XP_011518481.1
	XM_017017885.1	21	3811	XP_016873374.1
	XM_017017886.1	20	3776	XP_016873375.1
	XM_017017887.1	19	3556	XP_016873376.1
	XM_017017888.1	19	3728	XP_016873377.1
	XM_017017889.1	19	3728	XP_016873378.1
	XM_017017890.1	19	3725	XP_016873379.1
	XM_017017891.1	19	3635	XP_016873380.1
	XM_017017892.1	19	3635	XP_016873381.1
	XM_017017893.1	20	3768	XP_016873382.1
	XM_017017894.1	19	3590	XP_016873383.1
	XM_017017895.1	19	3587	XP_016873384.1
	XM_017017896.1	19	3587	XP_016873385.1
	XM_017017897.1	20	3808	XP_016873386.1
	XM_017017898.1	20	3666	XP_016873387.1
	XM_017017899.1	21	3800	XP_016873388.1
	XM_017017900.1	20	3755	XP_016873389.1
	XM_017017901.1	18	3575	XP_016873390.1
	XM_017017902.1	19	3494	XP_016873391.1
	XM_017017903.1	16	3144	XP_016873392.1
	XM_017017905.1	18	3479	XP_016873394.1
	XM_017017907.1	18	3386	XP_016873396.1
	XM_017017908.1	21	3899	XP_016873397.1
	AB051483.1	18	3432
	AF208848.1	10	2219	AAF64262.1
	AK023258.1	20	3449	BAB14492.1
	AL359593.1	1	853
	BX648236.1	10	5470	CAH10542.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv516442	Chr.11:45878411 - 45961834 on Build GRCh38	Loss	PEX16 MAPK8IP1 PHF21A C11orf94 CRY2 LARGE2

More Information

• Set Membership: Intragenic, Exonic, DGV Variation

Gene Ontology Categories:

Process(es)

transcription, DNA-templated
regulation of transcription, DNA-templated
blood coagulation
histone deacetylation

Function(s)

RNA polymerase II regulatory region sequence-specific DNA binding
chromatin binding
transcription cofactor activity
histone deacetylase activity
protein binding
zinc ion binding
histone binding