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See other SLC25A18 CNV Assays ›
Gene Symbol
SLC25A18
Assay Reference Genome
Location

Chr.22:17571315 on build GRCh38
Cytoband
22q11.21
Assay ID Hs05564496_cn
Size
Availability Made To Order
Catalog # 4400291
Price
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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 Intron 3
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 XP_011544451.1
XM_011546150.2 XP_011544452.1
XM_011546151.2 XP_011544453.1
XM_011546152.1 XP_011544454.1
XM_011546153.2 XP_011544455.1
XM_011546154.2 XP_011544456.1
XM_017028968.1 XP_016884457.1
XM_017028969.1 XP_016884458.1
XM_017028970.1 XP_016884459.1
XM_017028971.1 XP_016884460.1
XM_017028972.1 XP_016884461.1
XM_017028973.1 XP_016884462.1
XM_017028974.1 XP_016884463.1
XM_017028975.1 XP_016884464.1
AJ428203.1 CAD21008.1
AK095706.1
AK308974.1
AK309110.1
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
esv3568230 Chr.22:17570832 - 17577690 on Build GRCh38 Loss SLC25A18
nsv9871 Chr.22:17545048 - 17683541 on Build GRCh38 Loss CECR2 SLC25A18 BCL2L13 LOC101929372 ATP6V1E1
nsv526826 Chr.22:17411511 - 17836413 on Build GRCh38 Gain CECR2 SLC25A18 BCL2L13 LOC101929372 BID LINC00528 MICAL3 MIR3198-1 ATP6V1E1
nsv1065055 Chr.22:17559085 - 17632626 on Build GRCh38 Gain SLC25A18 BCL2L13 LOC101929372 ATP6V1E1
dgv4464n100 Chr.22:17570790 - 17611340 on Build GRCh38 Gain SLC25A18 LOC101929372 ATP6V1E1
nsv428385 Chr.22:17491941 - 18886703 on Build GRCh38 Gain+Loss USP18 LOC100996415 LOC102725072 LOC100996432 LINC00528 MIR3198-1 ATP6V1E1 GGT3P RIMBP3 LOC729461 LOC100996401 MIR648 PEX26 FLJ41941 CECR2 PI4KAP1 TMEM191B SLC25A18 BCL2L13 LOC101929372 LOC642643 FAM230A BID TUBA8 MICAL3
nsv510802 Chr.22:17550100 - 17604891 on Build GRCh38 Deletion CECR2 SLC25A18 LOC101929372 ATP6V1E1
nsv3553 Chr.22:17553601 - 17608096 on Build GRCh38 Deletion CECR2 SLC25A18 LOC101929372 ATP6V1E1

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More Information


Set Membership:

 Intragenic Intronic Non-exonic DGV Variation

Panther Classification:

Gene Ontology Categories:

Function(s) Process(es)


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