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Gene Symbol
BBOF1
Assay Reference Genome
Location

Chr.14:74020993 on build GRCh38
Cytoband
14q24.3
Assay ID Hs07102220_cn
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Availability Made To Order
Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 80127

Gene Name:

 basal body orientation factor 1

Gene Aliases:

 C14orf45, CCDC176

Location:

 Chr.14:74019350-74078351 on Build GRCh38

Assay Gene Location:

 Within Intron 2
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
BBOF1 NM_025057.2 NP_079333.2
XM_005268092.3 XP_005268149.1
XM_005268097.3 XP_005268154.1
XM_005268098.4 XP_005268155.1
XM_011537170.2 XP_011535472.1
XM_011537171.2 XP_011535473.1
XM_011537172.1 XP_011535474.1
XM_011537174.2 XP_011535476.1
XM_011537175.2 XP_011535477.1
XM_011537176.2 XP_011535478.1
XM_011537177.2 XP_011535479.1
XM_011537179.2 XP_011535481.1
XM_017021659.1 XP_016877148.1
XM_017021660.1 XP_016877149.1
XM_017021661.1 XP_016877150.1
XM_017021662.1 XP_016877151.1
XM_017021663.1 XP_016877152.1
DB484577.1
DB493409.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv1053281 Chr.14:73518500 - 74050155 on Build GRCh38 Gain HEATR4 BBOF1 ZNF410 MIR4505 DNAL1 ACOT2 ACOT1 ENTPD5 LOC100506498 COQ6 FAM161B PTGR2 PNMA1 ELMSAN1 ACOT4 LOC100506476 ACOT6
dgv1937n100 Chr.14:73950133 - 74115803 on Build GRCh38 Gain COQ6 FAM161B BBOF1 ALDH6A1 ENTPD5 LIN52
dgv1938n100 Chr.14:73984364 - 74075786 on Build GRCh38 Gain BBOF1 ALDH6A1 ENTPD5
nsv524396 Chr.14:73958235 - 74023032 on Build GRCh38 Gain COQ6 BBOF1 ENTPD5
nsv1046028 Chr.14:73957079 - 74032042 on Build GRCh38 Loss COQ6 BBOF1 ENTPD5

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More Information


Additional Information:

For this assay, SNP(s) [rs80177305] 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

Gene Ontology Categories:

Function(s)


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