Assay Details
Target Gene Details
Entrez Gene ID: | 80063 |
Gene Name: | activating transcription factor 7 interacting protein 2 |
Gene Aliases: |
MCAF2 |
Location: |
Chr.16:10386055-10483640 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
ATF7IP2 | NM_001256160.1 | NP_001243089.1 | ||
NM_024997.3 | NP_079273.2 | |||
NR_045816.1 | ||||
AK093414.1 | BAC04157.1 | |||
AK296565.1 | ||||
AK299040.1 | ||||
BC033891.1 | AAH33891.1 | |||
BI459223.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv1051406 | Chr.16:10365859 - 10570475 on Build GRCh38 | Loss |
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nsv519263 | Chr.16:10386989 - 10466528 on Build GRCh38 | Gain+Loss |
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dgv4907n54 | Chr.16:10388455 - 10504610 on Build GRCh38 | Loss |
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nsv1040428 | Chr.16:10145408 - 11362136 on Build GRCh38 | Gain |
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dgv2727n100 | Chr.16:9914166 - 10436036 on Build GRCh38 | Gain |
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More Information
Additional Information:
For this assay, SNP(s) [rs76640481] 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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