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See other DNAAF1 CNV Assays ›
Gene Symbol
DNAAF1
Assay Reference Genome
Location

Chr.16:84159709 on build GRCh38
Cytoband
16q24.1
Assay ID Hs03077423_cn
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Availability Made To Order
Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 123872

Gene Name:

 dynein axonemal assembly factor 1

Gene Aliases:

 CILD13, LRRC50, ODA7

Location:

 Chr.16:84145260-84178761 on Build GRCh38

Assay Gene Location:

 Overlaps Intron 6 - Exon 7
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
DNAAF1 NM_001318756.1 NP_001305685.1
NM_178452.5 NP_848547.4
XM_006721129.2 XP_006721192.1
XM_011522853.2 XP_011521155.1
XM_011522854.2 XP_011521156.1
XM_011522855.2 XP_011521157.1
XM_011522857.2 XP_011521159.1
XM_011522858.2 XP_011521160.1
XM_017022918.1 XP_016878407.1
XM_017022919.1 XP_016878408.1
XM_017022920.1 XP_016878409.1
XM_017022921.1 XP_016878410.1
XM_017022922.1 XP_016878411.1
AK057238.1 BAB71392.1
AK058059.1 BAB71645.1
AK295990.1
AK310961.1
AL833327.1
AL833328.1 CAH10390.1
AL833336.1 CAH10394.1
BC024009.2 AAH24009.3
BX648657.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv833309 Chr.16:84076867 - 84248591 on Build GRCh38 Loss KCNG4 TAF1C HSDL1 LOC729887 MBTPS1 DNAAF1 ADAD2
nsv1065790 Chr.16:83830329 - 84243597 on Build GRCh38 Loss KCNG4 TAF1C MLYCD OSGIN1 HSDL1 LOC729887 MBTPS1 SLC38A8 DNAAF1 ADAD2 LOC105371371 NECAB2
esv2761930 Chr.16:84007420 - 84312461 on Build GRCh38 Gain KCNG4 TAF1C HSDL1 LOC729887 MBTPS1 SLC38A8 DNAAF1 ADAD2 LOC105376777 WFDC1
nsv1059227 Chr.16:84029323 - 84233403 on Build GRCh38 Loss KCNG4 TAF1C HSDL1 LOC729887 MBTPS1 SLC38A8 DNAAF1 ADAD2

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More Information


Additional Information:

For this assay, SNP(s) [rs112051327] 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 Non-exonic DGV Variation

Panther Classification:

Gene Ontology Categories:

Function(s) Process(es)


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