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See other NDUFV1 CNV Assays ›
Gene Symbol
NDUFV1
Assay Reference Genome
Location

Chr.11:67611648 on build GRCh38
Cytoband
11q13.2
Assay ID Hs03784449_cn
Size
Availability Made To Order
Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 4723

Gene Name:

 NADH:ubiquinone oxidoreductase core subunit V1

Gene Aliases:

 CI-51K, CI51KD, UQOR1

Location:

 Chr.11:67606852-67612541 on Build GRCh38

Assay Gene Location:

 Within Intron 7
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
NDUFV1 NM_001166102.1 NP_001159574.1
NM_007103.3 NP_009034.2
AF053070.1 AAC39722.1
AF092131.1 AAD40373.1
AK055875.1
AK223061.1 BAD96781.1
AK293522.1
AK300726.1
AK316122.1
BC007619.1 AAH07619.1
BC008146.1 AAH08146.1
BC015645.2 AAH15645.1
CR456739.1 CAG33020.1
DB532599.1
S67973.1 AAB29698.2

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
dgv1981n54 Chr.11:67579272 - 68049469 on Build GRCh38 Gain MIR6753 DOC2GP GSTP1 C11orf72 ALDH3B1 ACY3 UNC93B1 NUDT8 NDUFS8 NDUFV1 TCIRG1 MIR4691 ALDH3B2 MIR7113 LOC105369360 FAM86C2P TBX10
esv2422195 Chr.11:67466851 - 67859430 on Build GRCh38 Duplication DOC2GP GSTP1 C11orf72 TMEM134 ACY3 MIR6752 NUDT8 PITPNM1 NDUFV1 CABP2 CDK2AP2 AIP ALDH3B2 FAM86C2P TBX10
dgv1982n54 Chr.11:67605006 - 67666398 on Build GRCh38 Loss DOC2GP NUDT8 NDUFV1 C11orf72 ACY3 ALDH3B2 TBX10
dgv1214n100 Chr.11:67552445 - 67996597 on Build GRCh38 Gain DOC2GP NUDT8 GSTP1 NDUFV1 C11orf72 ACY3 ALDH3B2 LOC105369360 FAM86C2P UNC93B1 TBX10
nsv951023 Chr.11:67608030 - 67649929 on Build GRCh38 Deletion DOC2GP NUDT8 NDUFV1 ACY3 TBX10
nsv468606 Chr.11:67585218 - 68049469 on Build GRCh38 Gain MIR6753 DOC2GP GSTP1 C11orf72 ALDH3B1 ACY3 UNC93B1 NUDT8 NDUFS8 NDUFV1 TCIRG1 MIR4691 ALDH3B2 MIR7113 LOC105369360 FAM86C2P TBX10

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More Information


Additional Information:

For this assay, SNP(s) [rs112015076] 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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