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See other CCDC66 CNV Assays ›
Gene Symbol
CCDC66
Assay Reference Genome
Location

Chr.3:56620547 on build GRCh38
Cytoband
3p14.3
Assay ID Hs02793692_cn
Size
Availability Made To Order
Catalog # 4400291
Price 4,505.00
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4505.0
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Assay Details

Target Gene Details

Entrez Gene ID:

 285331

Gene Name:

 coiled-coil domain containing 66

Gene Aliases:

 -

Location:

 Chr.3:56557125-56621837 on Build GRCh38

Assay Gene Location:

 Within Intron 21
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
CCDC66 NM_001012506.4 NP_001012524.4
NM_001141947.1 NP_001135419.1
NR_024460.1
XM_005265081.3 XP_005265138.1
XM_005265082.3 XP_005265139.1
XM_005265083.3 XP_005265140.1
XM_005265084.3 XP_005265141.1
XM_011533614.2 XP_011531916.1
XM_011533615.2 XP_011531917.1
XM_011533616.2 XP_011531918.1
XM_011533617.2 XP_011531919.1
XM_011533619.2 XP_011531921.1
XM_017006229.1 XP_016861718.1
XM_017006230.1 XP_016861719.1
XM_017006231.1 XP_016861720.1
XM_017006232.1 XP_016861721.1
XM_017006233.1 XP_016861722.1
XM_017006234.1 XP_016861723.1
XM_017006235.1 XP_016861724.1
XM_017006236.1 XP_016861725.1
XM_017006237.1 XP_016861726.1
XM_017006238.1 XP_016861727.1
XM_017006239.1 XP_016861728.1
XM_017006240.1 XP_016861729.1
XM_017006241.1 XP_016861730.1
XM_017006242.1 XP_016861731.1
XM_017006243.1 XP_016861732.1
XM_017006244.1 XP_016861733.1
XM_017006245.1 XP_016861734.1
AA887479.1
AK096754.1
AL832556.1
AL832692.1
AL833326.1
BC047509.1 AAH47509.1
BC132827.1
BU674751.1

Target Gene Details

Entrez Gene ID:

 23272

Gene Name:

 family with sequence similarity 208 member A

Gene Aliases:

 C3orf63, RAP140, se89-1

Location:

 Chr.3:56620132-56683242 on Build GRCh38

Assay Gene Location:

 Within Exon 24
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
FAM208A NM_001112736.1 24 7881 NP_001106207.1
NM_015224.3 17 6832 NP_056039.2
XM_005264999.1 24 7739 XP_005265056.1
AB029028.1 7 4685 BAA83057.1
AF180425.2 AAD55098.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv460557 Chr.3:56560707 - 56627292 on Build GRCh38 Loss FAM208A CCDC66

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More Information


Additional Information:

For this assay, SNP(s) [rs534538641] 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 Exonic Intronic Non-exonic DGV Variation

Gene Ontology Categories:

Function(s) Process(es)


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