Assay Details
Target Gene Details
Entrez Gene ID: | 22980 |
Gene Name: | transcription factor 25 |
Gene Aliases: |
FKSG26, Hulp1, NULP1, PRO2620, hKIAA1049 |
Location: |
Chr.16:89873583-89911384 on Build GRCh38 |
Assay Gene Location: | Within Intron 7 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv573744 | Chr.16:89738447 - 89915950 on Build GRCh38 | Loss | TCF25 SPIRE2 FANCA LOC105371419 ZNF276 LOC107984817 |
esv2758671 | Chr.16:89804324 - 89901541 on Build GRCh38 | Loss | TCF25 SPIRE2 FANCA LOC105371419 LOC107984817 |
esv2762221 | Chr.16:89610380 - 90039318 on Build GRCh38 | Gain+Loss | VPS9D1-AS1 DEF8 GAS8-AS1 SPIRE2 FANCA AFG3L1P SPATA33 DBNDD1 CDK10 ZNF276 TUBB3 VPS9D1 GAS8 TCF25 DPEP1 CHMP1A LOC105371419 SPATA2L MC1R LOC107984817 CENPBD1 |
nsv573810 | Chr.16:89857498 - 90037251 on Build GRCh38 | Loss | DEF8 TCF25 GAS8-AS1 SPIRE2 AFG3L1P DBNDD1 TUBB3 MC1R CENPBD1 GAS8 |
nsv428331 | Chr.16:89216635 - 90185980 on Build GRCh38 | Gain+Loss | FAM157C VPS9D1-AS1 FANCA LOC105371414 SPATA33 CPNE7 DBNDD1 ZNF276 VPS9D1 PRDM7 TCF25 CHMP1A SPATA2L SPG7 CENPBD1 URAHP DEF8 RPL13 SNORD68 ZNF778 GAS8-AS1 SPIRE2 AFG3L1P LOC100287036 CDK10 TUBB8P7 TUBB3 GAS8 LOC101927817 DPEP1 ANKRD11 LOC105371419 MC1R LOC107984817 |
nsv573799 | Chr.16:89852186 - 90022379 on Build GRCh38 | Gain | DEF8 TCF25 SPIRE2 AFG3L1P DBNDD1 LOC105371419 TUBB3 MC1R CENPBD1 GAS8 |
nsv482951 | Chr.16:88633593 - 90228345 on Build GRCh38 | Loss | CBFA2T3 FANCA LOC105371414 CPNE7 DBNDD1 ZNF276 VPS9D1 PRDM7 TCF25 CHMP1A LINC00304 SPG7 CENPBD1 LOC400558 RNF166 DEF8 RPL13 SNORD68 GAS8-AS1 AFG3L1P TUBB3 GAS8 ACSF3 SNAI3 DPEP1 ANKRD11 LOC100129697 MVD MC1R FAM157C MIR4722 VPS9D1-AS1 SPATA33 CYBA LOC339059 LOC105371409 LOC107987238 SLC22A31 PIEZO1 LOC100289580 SPATA2L GALNS APRT URAHP CDH15 IL17C CDT1 ZNF778 LOC101927793 SPIRE2 LOC100287036 CDK10 TUBB8P7 TRAPPC2L LOC101927817 PABPN1L SNAI3-AS1 CTU2 LOC105371419 LOC107984817 |
More Information
Set Membership: |
Intragenic Intronic Non-exonic DGV Variation |