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See other PHF21A CNV Assays ›
Gene Symbol
PHF21A
Assay Reference Genome
Location

Chr.11:45939727 on build GRCh38
Cytoband
11p11.2
Assay ID Hs05237236_cn
Size
Availability Made To Order
Catalog # 4400291
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Assay Details

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 Intron 22
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
PHF21A NM_001101802.1 NP_001095272.1
NM_016621.3 NP_057705.3
XM_005252965.4 XP_005253022.1
XM_011520157.2 XP_011518459.1
XM_011520158.2 XP_011518460.1
XM_011520160.2 XP_011518462.1
XM_011520161.2 XP_011518463.1
XM_011520162.2 XP_011518464.1
XM_011520164.2 XP_011518466.1
XM_011520165.2 XP_011518467.1
XM_011520166.2 XP_011518468.1
XM_011520167.2 XP_011518469.1
XM_011520168.2 XP_011518470.1
XM_011520169.2 XP_011518471.1
XM_011520173.2 XP_011518475.1
XM_011520174.2 XP_011518476.1
XM_011520175.2 XP_011518477.1
XM_011520179.2 XP_011518481.1
XM_017017885.1 XP_016873374.1
XM_017017886.1 XP_016873375.1
XM_017017887.1 XP_016873376.1
XM_017017888.1 XP_016873377.1
XM_017017889.1 XP_016873378.1
XM_017017890.1 XP_016873379.1
XM_017017891.1 XP_016873380.1
XM_017017892.1 XP_016873381.1
XM_017017893.1 XP_016873382.1
XM_017017894.1 XP_016873383.1
XM_017017895.1 XP_016873384.1
XM_017017896.1 XP_016873385.1
XM_017017897.1 XP_016873386.1
XM_017017898.1 XP_016873387.1
XM_017017899.1 XP_016873388.1
XM_017017900.1 XP_016873389.1
XM_017017901.1 XP_016873390.1
XM_017017902.1 XP_016873391.1
XM_017017903.1 XP_016873392.1
XM_017017904.1 XP_016873393.1
XM_017017905.1 XP_016873394.1
XM_017017906.1 XP_016873395.1
XM_017017907.1 XP_016873396.1
XM_017017908.1 XP_016873397.1
AB051483.1
AF208848.1 AAF64262.1
AK023258.1 BAB14492.1
AY090777.1 AAM09095.1
BC015714.2 AAH15714.1
BX648236.1 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 C11orf94 MAPK8IP1 LARGE2 CRY2 PHF21A

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More Information


Additional Information:

For this assay, SNP(s) [rs79981700] 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

Gene Ontology Categories:

Function(s) Process(es)


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