Assay Details
Target Gene Details
Entrez Gene ID: | 11102 |
Gene Name: | ribonuclease P/MRP subunit p14 |
Gene Aliases: |
HsHTD2, P14 |
Location: |
Chr.3:58306245-58322642 on Build GRCh38 |
Assay Gene Location: | Within Exon 7 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
RPP14 | NM_001098783.2 | 6 | 2543 | NP_001092253.1 |
NM_007042.4 | 6 | 2309 | NP_008973.1 | |
NR_049755.1 | 5 | 2445 | ||
NR_049756.1 | 6 | 2309 | ||
NR_049757.1 | 5 | 2211 | ||
NR_049758.1 | 4 | 2126 | ||
XM_011533313.2 | 6 | 2343 | XP_011531615.1 | |
XM_017005641.1 | 6 | 2306 | XP_016861130.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv528147 | Chr.3:57929747 - 58384450 on Build GRCh38 | Gain |
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nsv590369 | Chr.3:58283985 - 58331965 on Build GRCh38 | Loss |
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dgv4748n100 | Chr.3:58316064 - 58399467 on Build GRCh38 | Gain |
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nsv1001814 | Chr.3:58158881 - 58354197 on Build GRCh38 | Gain |
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More Information
Additional Information:
For this assay, SNP(s) [rs114100127] 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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Gene Ontology Categories:
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