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See other NDUFS7 CNV Assays ›
Gene Symbol
NDUFS7
Assay Reference Genome
Location

Chr.19:1394182 on build GRCh38
Cytoband
19p13.3
Assay ID Hs04032838_cn
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Availability Made To Order
Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 374291

Gene Name:

 NADH:ubiquinone oxidoreductase core subunit S7

Gene Aliases:

 CI-20, CI-20KD, MY017, PSST

Location:

 Chr.19:1383571-1395589 on Build GRCh38

Assay Gene Location:

 Within Intron 7
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
NDUFS7 NM_024407.4 NP_077718.3
XM_005259556.4 XP_005259613.2
AF060512.1 AAG43130.1
AF115969.1 AAP97240.1
AK056061.1 1 784
AK091024.1 6 1648
AK091046.1 1 2341
AK091623.1 7 1419
AK092169.1 6 1687 BAC03820.1
AK127759.1 BAC87117.1
AK128713.1 5 1954 BAC87587.1
AK222738.1 BAD96458.1
AK293917.1
BC001715.3 AAH01715.2
BC005954.1 AAH05954.1
BC111517.1 AAI11518.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
esv32942 Chr.19:1320268 - 1999205 on Build GRCh38 Gain+Loss SCAMP4 PCSK4 MUM1 REXO1 MIR1909 ABHD17A LOC100288123 RPS15 C19orf25 PLK5 KLF16 DAZAP1 ONECUT3 UQCR11 REEP6 CSNK1G2 ADAMTSL5 GAMT ATP8B3 TCF3 MEX3D APC2 BTBD2 MBD3 CSNK1G2-AS1 ADAT3 NDUFS7
nsv833705 Chr.19:1380125 - 1544934 on Build GRCh38 Loss PLK5 APC2 PCSK4 ADAMTSL5 DAZAP1 RPS15 C19orf25 NDUFS7 GAMT REEP6
nsv482207 Chr.19:1383884 - 1395589 on Build GRCh38 Gain NDUFS7
esv3643389 Chr.19:1264454 - 1397379 on Build GRCh38 Gain C19orf24 MUM1 EFNA2 CIRBP CIRBP-AS1 NDUFS7 GAMT
esv2758743 Chr.19:951641 - 1544934 on Build GRCh38 Gain+Loss C19orf24 PCSK4 MUM1 TMEM259 GPX4 LOC102725180 STK11 RPS15 C19orf25 ATP5D PLK5 POLR2E DAZAP1 SBNO2 GRIN3B REEP6 LOC105372235 WDR18 EFNA2 ARID3A CNN2 ADAMTSL5 CBARP MIDN GAMT APC2 ABCA7 CIRBP CIRBP-AS1 RNU6-2 NDUFS7 ARHGAP45
nsv953942 Chr.19:1371602 - 2057401 on Build GRCh38 Deletion SCAMP4 PCSK4 MUM1 REXO1 MIR1909 ABHD17A LOC100288123 RPS15 C19orf25 PLK5 KLF16 DAZAP1 ONECUT3 UQCR11 REEP6 CSNK1G2 ADAMTSL5 GAMT ATP8B3 TCF3 MEX3D APC2 BTBD2 MBD3 MKNK2 CSNK1G2-AS1 ADAT3 NDUFS7
esv3643396 Chr.19:1356856 - 1396468 on Build GRCh38 Gain MUM1 NDUFS7
nsv578278 Chr.19:1371355 - 1448181 on Build GRCh38 Loss APC2 MUM1 DAZAP1 RPS15 NDUFS7 GAMT

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More Information


Additional Information:

For this assay, SNP(s) [rs376591934] 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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