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Gene Symbol
PHYHIP
Assay Reference Genome
Location

Chr.8:22220367 on build GRCh38
Cytoband
8p21.3
Assay ID Hs01320538_cn
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Availability Made To Order
Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 9796

Gene Name:

 phytanoyl-CoA 2-hydroxylase interacting protein

Gene Aliases:

 DYRK1AP3, PAHX-AP, PAHXAP1

Location:

 Chr.8:22219703-22232338 on Build GRCh38

Assay Gene Location:

 Within Exon 7
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
PHYHIP NM_001099335.1 6 2673 NP_001092805.1
NM_014759.3 5 2551 NP_055574.3
XM_006716416.1 XP_006716479.1
XM_017014102.1 3 2816 XP_016869591.1
AK098743.1
BC034034.1 5 2304 AAH34034.1
BC035940.1 5 2304 AAH35940.1
D87463.1 6 2382

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv470205 Chr.8:22191277 - 22256052 on Build GRCh38 Loss PHYHIP LOC100507071 BMP1 MIR320A POLR3D
dgv12054n54 Chr.8:22045805 - 22251098 on Build GRCh38 Loss NUDT18 FAM160B2 PHYHIP SFTPC HR FGF17 REEP4 BMP1 MIR320A DMTN LGI3 POLR3D
nsv831265 Chr.8:22199688 - 22366918 on Build GRCh38 Loss PHYHIP LOC100507071 BMP1 MIR320A PIWIL2 POLR3D
nsv831264 Chr.8:22093700 - 22328040 on Build GRCh38 Gain+Loss NUDT18 FAM160B2 PHYHIP SFTPC LOC100507071 HR REEP4 BMP1 MIR320A LGI3 PIWIL2 POLR3D
esv2759604 Chr.8:20675533 - 23254096 on Build GRCh38 Loss NUDT18 SFTPC C8orf58 RHOBTB2 HR REEP4 LOC254896 LOC286059 LOC286114 TNFRSF10B LOC100507071 LOC107984124 LOC102467222 NPM2 LOC389641 SLC39A14 BIN3-IT1 PPP3CC TNFRSF10C TNFRSF10D EGR3 BIN3 SORBS3 CHMP7 DMTN LGI3 XPO7 PIWIL2 DOK2 POLR3D FAM160B2 PHYHIP PEBP4 PDLIM2 GFRA2 LOC101929172 FGF17 BMP1 CCAR2 LOC101929237 MIR320A LOC107986876 TNFRSF10A

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More Information


Additional Information:

For this assay, SNP(s) [rs73551785] 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 DGV Variation

Gene Ontology Categories:

Function(s)


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