Assay Details
Target Gene Details
Entrez Gene ID: | 83733 |
Gene Name: | solute carrier family 25 member 18 |
Gene Aliases: |
GC2 |
Location: |
Chr.22:17562470-17590890 on Build GRCh38 |
Assay Gene Location: | Within Exon 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
SLC25A18 | NM_001303484.1 | NP_001290413.1 | ||
NM_031481.2 | NP_113669.1 | |||
XM_011546149.2 | 1 | 1003 | XP_011544451.1 | |
XM_011546150.2 | 1 | 1005 | XP_011544452.1 | |
XM_011546153.2 | 1 | 1005 | XP_011544455.1 | |
XM_017028969.1 | 1 | 999 | XP_016884458.1 | |
XM_017028970.1 | 1 | 999 | XP_016884459.1 | |
XM_017028971.1 | 1 | 999 | XP_016884460.1 | |
XM_017028972.1 | 1 | 999 | XP_016884461.1 | |
XM_017028973.1 | 1 | 999 | XP_016884462.1 | |
XM_017028974.1 | 1 | 999 | XP_016884463.1 | |
XM_017028975.1 | 1 | 999 | XP_016884464.1 | |
AJ428203.1 | CAD21008.1 | |||
AK308974.1 | ||||
AY008285.1 | AAG22855.1 | |||
BC031644.1 | AAH31644.1 | |||
DA354203.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv9871 | Chr.22:17545048 - 17683541 on Build GRCh38 | Loss | BCL2L13 ATP6V1E1 LOC101929372 SLC25A18 CECR2 |
nsv1065055 | Chr.22:17559085 - 17632626 on Build GRCh38 | Gain | BCL2L13 ATP6V1E1 LOC101929372 SLC25A18 |
nsv526826 | Chr.22:17411511 - 17836413 on Build GRCh38 | Gain | LINC00528 MIR3198-1 BCL2L13 BID ATP6V1E1 LOC101929372 SLC25A18 MICAL3 CECR2 |
nsv3553 | Chr.22:17553601 - 17608096 on Build GRCh38 | Deletion | ATP6V1E1 LOC101929372 SLC25A18 CECR2 |
nsv510802 | Chr.22:17550100 - 17604891 on Build GRCh38 | Deletion | ATP6V1E1 LOC101929372 SLC25A18 CECR2 |
nsv428385 | Chr.22:17491941 - 18886703 on Build GRCh38 | Gain+Loss | LINC00528 LOC100996432 LOC101929372 LOC100996401 LOC642643 FLJ41941 BCL2L13 BID MIR648 RIMBP3 TMEM191B LOC102725072 GGT3P MIR3198-1 SLC25A18 LOC100996415 PEX26 ATP6V1E1 TUBA8 FAM230A LOC729461 MICAL3 USP18 PI4KAP1 CECR2 |
More Information
Set Membership: |
Intragenic Exonic DGV Variation |