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 11 |
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_045815.1 | ||||
NR_045816.1 | ||||
XM_006720953.3 | XP_006721016.1 | |||
XM_011522666.2 | XP_011520968.1 | |||
XM_017023705.1 | XP_016879194.1 | |||
XM_017023706.1 | XP_016879195.1 | |||
XM_017023707.1 | XP_016879196.1 | |||
XM_017023708.1 | XP_016879197.1 | |||
XM_017023709.1 | XP_016879198.1 | |||
XM_017023710.1 | XP_016879199.1 | |||
XM_017023711.1 | XP_016879200.1 | |||
AK022730.1 | BAB14209.1 | |||
AK093414.1 | BAC04157.1 | |||
AK223492.1 | BAD97212.1 | |||
AK296565.1 | ||||
AK299040.1 | ||||
AL832987.1 | CAH56323.1 | |||
AY560615.1 | AAT66299.1 | |||
BC033891.1 | AAH33891.1 | |||
BC069695.1 | AAH69695.1 | |||
BC069713.1 | AAH69713.1 | |||
BC069730.1 | AAH69730.1 | |||
BC137079.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv571451 | Chr.16:10435543 - 10495488 on Build GRCh38 | Loss | ATF7IP2 |
nsv1051406 | Chr.16:10365859 - 10570475 on Build GRCh38 | Loss | ATF7IP2 EMP2 |
nsv519263 | Chr.16:10386989 - 10466528 on Build GRCh38 | Gain+Loss | ATF7IP2 |
dgv4907n54 | Chr.16:10388455 - 10504610 on Build GRCh38 | Loss | ATF7IP2 |
esv3637901 | Chr.16:10454025 - 10471134 on Build GRCh38 | Loss | ATF7IP2 |
nsv1036128 | Chr.16:10404948 - 10470444 on Build GRCh38 | Loss | ATF7IP2 |
nsv1040428 | Chr.16:10145408 - 11362136 on Build GRCh38 | Gain | DEXI ATF7IP2 EMP2 CIITA TVP23A PRM1 LOC107984859 RMI2 CLEC16A SOCS1 TEKT5 PRM3 LOC105371083 NUBP1 GRIN2A MIR548H2 PRM2 TNP2 |
nsv833139 | Chr.16:10442373 - 10477353 on Build GRCh38 | Loss | ATF7IP2 |
More Information
Set Membership: |
Intragenic Intronic Non-exonic DGV Variation |