Assay Details
Target Gene Details
Entrez Gene ID: | 22838 |
Gene Name: | ring finger protein 44 |
Gene Aliases: |
- |
Location: |
Chr.5:176526699-176543456 on Build GRCh38 |
Assay Gene Location: | Overlaps - Exon 14 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
RNF44 | NM_014901.4 | NP_055716.1 | ||
XM_005265840.2 | XP_005265897.1 | |||
XM_005265841.4 | XP_005265898.1 | |||
XM_005265842.4 | XP_005265899.1 | |||
XM_005265843.2 | XP_005265900.1 | |||
XM_005265844.3 | XP_005265901.1 | |||
XM_005265845.4 | XP_005265902.1 | |||
XM_006714831.2 | XP_006714894.1 | |||
XM_006714832.2 | XP_006714895.1 | |||
XM_011534466.2 | XP_011532768.1 | |||
XM_011534467.2 | XP_011532769.1 | |||
AB029023.1 | ||||
AK127673.1 | BAC87078.1 | |||
BC039833.1 | AAH39833.1 | |||
BC063297.1 | AAH63297.1 | |||
BM672494.1 | ||||
Z39041.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv471056 | Chr.5:176520050 - 176597879 on Build GRCh38 | Loss |
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nsv950722 | Chr.5:176517300 - 176533099 on Build GRCh38 | Deletion |
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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) [rs78282406] 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:
![](/order/genome-database/details/genotyping/assets/img/arrow_icon_up_black.png)