Assay Details
Target Gene Details
Entrez Gene ID: | 7023 |
Gene Name: | transcription factor AP-4 (activating enhancer binding protein 4) |
Gene Aliases: |
AP-4, bHLHc41 |
Location: |
Chr.16:4257186-4273000 on Build GRCh38 |
Assay Gene Location: | Within Intron 3 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
TFAP4 | NM_003223.2 | NP_003214.1 | ||
XM_011522633.2 | XP_011520935.1 | |||
XM_011522635.2 | XP_011520937.1 | |||
AB209146.1 | 1 | 3836 | BAD92383.1 | |
AK309301.1 | ||||
BC010576.1 | AAH10576.1 | |||
BU159415.1 | ||||
CR541726.1 | CAG46527.1 | |||
DA449763.1 | ||||
S73885.1 | AAB32235.1 | |||
X57435.1 | CAA40683.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv1046986 | Chr.16:4049000 - 5555721 on Build GRCh38 | Gain |
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esv21490 | Chr.16:3825338 - 4270692 on Build GRCh38 | Gain+Loss |
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nsv527866 | Chr.16:4206462 - 4412618 on Build GRCh38 | Loss |
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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) [rs73503284] 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:
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