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Gene Symbol
PCM1
Assay Reference Genome
Location

Chr.8:17944744 on build GRCh38
Cytoband
8p22
Assay ID Hs06169002_cn
Size
Availability Made To Order
Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 5108

Gene Name:

 pericentriolar material 1

Gene Aliases:

 PTC4, RET/PCM-1

Location:

 Chr.8:17922763-18029948 on Build GRCh38

Assay Gene Location:

 Within Intron 10
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
PCM1 NM_001315507.1 NP_001302436.1
NM_001315508.1 NP_001302437.1
NM_006197.3 NP_006188.3
XM_006716336.3 XP_006716399.1
XM_006716340.3 XP_006716403.1
XM_006716349.3 XP_006716412.1
XM_011544528.2 XP_011542830.1
XM_011544529.2 XP_011542831.1
XM_011544530.2 XP_011542832.1
XM_011544532.2 XP_011542834.1
XM_011544533.2 XP_011542835.1
XM_011544534.2 XP_011542836.1
XM_011544535.2 XP_011542837.1
XM_011544540.2 XP_011542842.1
XM_017013472.1 XP_016868961.1
XM_017013473.1 XP_016868962.1
XM_017013474.1 XP_016868963.1
XM_017013475.1 XP_016868964.1
XM_017013476.1 XP_016868965.1
XM_017013477.1 XP_016868966.1
XM_017013478.1 XP_016868967.1
XM_017013479.1 XP_016868968.1
XM_017013480.1 XP_016868969.1
XM_017013481.1 XP_016868970.1
XM_017013482.1 XP_016868971.1
XM_017013483.1 XP_016868972.1
XM_017013484.1 XP_016868973.1
XM_017013485.1 XP_016868974.1
XM_017013486.1 XP_016868975.1
XM_017013487.1 XP_016868976.1
XM_017013488.1 XP_016868977.1
XM_017013489.1 XP_016868978.1
XM_017013490.1 XP_016868979.1
XM_017013491.1 XP_016868980.1
XM_017013492.1 XP_016868981.1
XM_017013493.1 XP_016868982.1
XM_017013494.1 XP_016868983.1
XM_017013495.1 XP_016868984.1
XM_017013496.1 XP_016868985.1
XM_017013497.1 XP_016868986.1
XM_017013498.1 XP_016868987.1
XM_017013499.1 XP_016868988.1
XM_017013500.1 XP_016868989.1
XM_017013501.1 XP_016868990.1
XM_017013502.1 XP_016868991.1
XM_017013503.1 XP_016868992.1
XM_017013504.1 XP_016868993.1
XM_017013505.1 XP_016868994.1
XM_017013506.1 XP_016868995.1
XM_017013507.1 XP_016868996.1
XM_017013508.1 XP_016868997.1
AK307583.1
AX785390.1 CAE11958.1
BC000453.2 AAH00453.1
BC027477.1 AAH27477.1
BC065022.1 AAH65022.1
BC133052.1
BC140946.1
L27841.1 AAA60120.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
dgv7121n100 Chr.8:17766079 - 17957752 on Build GRCh38 Gain FGL1 MTUS1 PCM1
nsv610701 Chr.8:17787519 - 17956578 on Build GRCh38 Gain FGL1 MTUS1 PCM1
esv3616500 Chr.8:17771011 - 17959017 on Build GRCh38 Gain FGL1 MTUS1 PCM1
esv2762735 Chr.8:17723646 - 17957764 on Build GRCh38 Gain FGL1 MTUS1 PCM1

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More Information


Additional Information:

For this assay, SNP(s) [rs114117677,rs116956692] 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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