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See other CSNK1D CNV Assays ›
Gene Symbol
CSNK1D
Assay Reference Genome
Location

Chr.17:82250392 on build GRCh38
Cytoband
17q25.3
Assay ID Hs04463593_cn
Size
Availability Made To Order
Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 1453

Gene Name:

 casein kinase 1 delta

Gene Aliases:

 ASPS, CKIdelta, FASPS2, HCKID

Location:

 Chr.17:82239317-82273742 on Build GRCh38

Assay Gene Location:

 Within Intron 7
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
CSNK1D NM_001893.4 NP_001884.2
NM_139062.2 NP_620693.1
NR_110578.1
XM_005256336.3 XP_005256393.1
XM_005256337.4 XP_005256394.1
XM_017024199.1 XP_016879688.1
AB091044.1 BAC10903.1
AB209463.1 BAD92700.1
AK291758.1
AK295638.1
AK296969.1
AK303365.1
AK308852.1
AK311248.1
BC003558.1 AAH03558.1
BC015775.1 AAH15775.1
U29171.1 AAC50807.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv428351 Chr.17:81152631 - 83064073 on Build GRCh38 Gain MIR6786 ANAPC11 SLC25A10 NPLOC4 C17orf62 BAHCC1 TEPSIN OGFOD3 CEP131 FASN SNORD134 FOXK2 SLC16A3 TEX19 ARL16 HEXDC LOC105376791 AATK-AS1 NOTUM LOC100130370 NPB ASPSCR1 CCDC57 MRPL12 LOC105376790 B3GNTL1 NARF PPP1R27 PYCR1 HGS LOC101929511 TBCD GCGR MAFG-AS1 CCDC137 ARHGDIA AATK SLC38A10 ALYREF UTS2R FN3KRP SIRT7 STRA13 FAAP100 LOC105371925 MYADML2 FN3K CSNK1D PCYT2 ZNF750 ACTG1 WDR45B RAB40B CD7 SECTM1 LOC105371944 GPS1 PDE6G MAFG MIR3186 FSCN2 LINC00482 P4HB MCRIP1 DCXR MIR4740 LRRC45 C17orf89 DUS1L OXLD1 MIR4525 RFNG TSPAN10 MIR6787 TMEM105 LOC101929552 RAC3
nsv833572 Chr.17:82204977 - 82388835 on Build GRCh38 Loss CSNK1D LOC101929511 UTS2R CD7 MIR6787 CCDC57 SECTM1 SLC16A3 LOC105376790 TEX19
esv2762577 Chr.17:82244836 - 82838431 on Build GRCh38 Gain+Loss LOC105376791 UTS2R C17orf62 FN3KRP LOC105376790 NARF OGFOD3 FN3K CSNK1D MIR4525 ZNF750 LOC101929511 TBCD WDR45B RAB40B CD7 SECTM1 FOXK2 LOC101929552 TEX19 HEXDC
esv21913 Chr.17:81828123 - 83103548 on Build GRCh38 Gain+Loss ANAPC11 C17orf62 METRNL OGFOD3 FASN SNORD134 FOXK2 SLC16A3 TEX19 HEXDC LOC105376791 NOTUM NPB ASPSCR1 CCDC57 LOC105376790 B3GNTL1 NARF PPP1R27 PYCR1 LOC101929511 TBCD MAFG-AS1 ARHGDIA ALYREF UTS2R FN3KRP SIRT7 STRA13 MYADML2 FN3K CSNK1D PCYT2 ZNF750 WDR45B RAB40B CD7 SECTM1 LOC105371944 GPS1 MAFG P4HB MCRIP1 DCXR LRRC45 DUS1L MIR4525 RFNG MIR6787 LOC101929552 RAC3

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More Information


Additional Information:

For this assay, SNP(s) [rs73366234,rs73366236] 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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