Assay Details
Target Gene Details
Entrez Gene ID: | 57060 |
Gene Name: | poly(rC) binding protein 4 |
Gene Aliases: |
CBP, LIP4, MCG10 |
Location: |
Chr.3:51957454-51967466 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
PCBP4 | NM_001174100.1 | NP_001167571.1 | ||
NM_020418.3 | NP_065151.2 | |||
NM_033008.2 | NP_127501.1 | |||
XM_005265331.2 | XP_005265388.1 | |||
XM_006713269.1 | XP_006713332.1 | |||
XM_006713270.1 | XP_006713333.1 | |||
XM_017006916.1 | XP_016862405.1 | |||
XM_017006919.1 | XP_016862408.1 | |||
XM_017006920.1 | XP_016862409.1 | |||
AK001244.1 | ||||
AK023993.1 | BAB14761.1 | |||
AK225815.1 | ||||
BC003008.1 | AAH03008.1 | |||
BC004153.2 | AAH04153.1 | |||
BC017098.1 | AAH17098.1 | |||
DA074216.1 | ||||
DA701799.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv1003453 | Chr.3:51928065 - 52065425 on Build GRCh38 | Gain |
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nsv508922 | Chr.3:51940932 - 52009520 on Build GRCh38 | Insertion |
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nsv954857 | Chr.3:51932485 - 52056584 on Build GRCh38 | Deletion |
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nsv520211 | Chr.3:51738331 - 52132131 on Build GRCh38 | Gain |
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![](/order/genome-database/details/genotyping/assets/img/arrow_icon_up_black.png)
More Information
Additional Information:
For this assay, SNP(s) [rs80093522] 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: |
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Panther Classification:
Gene Ontology Categories:
![](/order/genome-database/details/genotyping/assets/img/arrow_icon_up_black.png)