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See other SLC25A10 CNV Assays ›
Gene Symbol
SLC25A10
Assay Reference Genome
Location

Chr.17:81713744 on build GRCh38
Cytoband
17q25.3
Assay ID Hs03965344_cn
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Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 1468

Gene Name:

 solute carrier family 25 member 10

Gene Aliases:

 DIC

Location:

 Chr.17:81712236-81721016 on Build GRCh38

Assay Gene Location:

 Within Intron 2
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
SLC25A10 NM_001270888.1 NP_001257817.1
NM_001270953.1 NP_001257882.1
NM_012140.4 NP_036272.2
XM_017024220.1 XP_016879709.1
AI081980.1
AJ131613.1 CAB59892.1
AK075249.1 BAC11497.1
AK303808.1
BC007355.2 AAH07355.1
BC015797.1 AAH15797.1
BM561945.1
KU177998.1
KU177999.1
KU178000.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
esv26223 Chr.17:80659041 - 81736487 on Build GRCh38 Gain+Loss MIR4740 OXLD1 SLC38A10 MIR3186 FAAP100 C17orf89 MIR3065 CCDC137 LOC105371925 LOC101928855 MIR657 MIR338 CEP131 SLC25A10 ARL16 MIR1250 CHMP6 LOC107985021 MRPL12 LOC100129503 AATK-AS1 TMEM105 LOC400627 BAIAP2-AS1 LOC105371921 LOC107985022 TEPSIN ACTG1 TSPAN10 LINC00482 BAIAP2 NPLOC4 AATK HGS BAHCC1 MIR6786 PDE6G LOC100130370 FSCN2 RPTOR
nsv428351 Chr.17:81152631 - 83064073 on Build GRCh38 Gain MIR4740 LRRC45 OXLD1 SLC38A10 MIR3186 FAAP100 C17orf89 ALYREF NOTUM LOC105376791 CD7 MCRIP1 CCDC137 LOC101929511 PYCR1 GCGR CEP131 ARL16 MRPL12 SLC16A3 TMEM105 MIR4525 UTS2R P4HB B3GNTL1 OGFOD3 NPB TEPSIN ACTG1 SIRT7 CSNK1D C17orf62 STRA13 ZNF750 RAC3 MYADML2 AATK DUS1L HGS GPS1 ARHGDIA MAFG-AS1 BAHCC1 MIR6786 LOC100130370 FSCN2 RAB40B SECTM1 MAFG PCYT2 WDR45B MIR6787 LOC105371925 ASPSCR1 LOC105376790 SNORD134 PPP1R27 SLC25A10 CCDC57 RFNG AATK-AS1 TBCD FOXK2 LOC101929552 FN3KRP DCXR TSPAN10 LINC00482 ANAPC11 FASN HEXDC TEX19 NPLOC4 LOC105371944 FN3K NARF PDE6G
nsv470620 Chr.17:81516973 - 82064485 on Build GRCh38 Loss LRRC45 OXLD1 FAAP100 ALYREF NOTUM MAFG MCRIP1 PCYT2 CCDC137 ASPSCR1 PYCR1 GCGR PPP1R27 SLC25A10 ARL16 RFNG MRPL12 P4HB NPB DCXR SIRT7 TSPAN10 ANAPC11 STRA13 RAC3 MYADML2 NPLOC4 DUS1L HGS GPS1 ARHGDIA MAFG-AS1 MIR6786 PDE6G FSCN2
nsv952390 Chr.17:81637175 - 81860124 on Build GRCh38 Deletion OXLD1 MCRIP1 TSPAN10 CCDC137 GCGR PPP1R27 SLC25A10 HGS ARL16 MIR6786 MRPL12 PDE6G P4HB

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More Information


Additional Information:

For this assay, SNP(s) [rs73354156] 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:

 Intragenic Intronic Non-exonic DGV Variation

Panther Classification:

Gene Ontology Categories:

Function(s) Process(es)


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