accessibility menu, dialog, popup

UserName
Viewing profile as user:

Please enter the information below and press OK to send your cart to Core Services for purchase.

    

System Message

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

Chr.17:82252066 on build GRCh38
Cytoband
17q25.3
Assay ID Hs03963476_cn
Size
Availability Made To Order
Catalog # 4400291
Price
Your Price
Online offer:
Check your price ›

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 6
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
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 SLC38A10 MCRIP1 DUS1L ASPSCR1 TEPSIN LOC101929511 FAAP100 MIR6787 UTS2R MRPL12 CEP131 ZNF750 OXLD1 LRRC45 CSNK1D MAFG STRA13 LOC105376791 CCDC137 MIR4525 DCXR ALYREF LINC00482 LOC101929552 CCDC57 PYCR1 NOTUM MYADML2 LOC105371944 FASN HGS NARF TMEM105 MAFG-AS1 LOC105371925 OGFOD3 MIR3186 RAB40B FOXK2 RAC3 TSPAN10 SECTM1 ARHGDIA TBCD FSCN2 MIR4740 FN3K GCGR B3GNTL1 SIRT7 LOC105376790 BAHCC1 AATK-AS1 ARL16 GPS1 RFNG C17orf89 C17orf62 SLC25A10 PPP1R27 ACTG1 NPB PCYT2 ANAPC11 TEX19 HEXDC FN3KRP SNORD134 LOC100130370 NPLOC4 WDR45B P4HB PDE6G MIR6786 SLC16A3 AATK CD7
nsv828139 Chr.17:82251362 - 82267313 on Build GRCh38 Loss CSNK1D
nsv469561 Chr.17:82251148 - 82472274 on Build GRCh38 Loss NARF CSNK1D LOC101929511 OGFOD3 SECTM1 TEX19 C17orf62 HEXDC UTS2R LOC105376790 CD7
nsv833572 Chr.17:82204977 - 82388835 on Build GRCh38 Loss CCDC57 CSNK1D LOC101929511 SECTM1 TEX19 MIR6787 UTS2R SLC16A3 LOC105376790 CD7
esv2762577 Chr.17:82244836 - 82838431 on Build GRCh38 Gain+Loss LOC101929511 SECTM1 TEX19 TBCD FN3K HEXDC UTS2R FN3KRP LOC105376790 ZNF750 NARF WDR45B CSNK1D OGFOD3 LOC105376791 C17orf62 MIR4525 RAB40B FOXK2 CD7 LOC101929552
esv21913 Chr.17:81828123 - 83103548 on Build GRCh38 Gain+Loss MCRIP1 DUS1L ASPSCR1 LOC101929511 MIR6787 UTS2R ZNF750 LRRC45 CSNK1D MAFG STRA13 LOC105376791 MIR4525 DCXR ALYREF LOC101929552 CCDC57 PYCR1 NOTUM MYADML2 LOC105371944 FASN NARF MAFG-AS1 OGFOD3 RAB40B FOXK2 RAC3 SECTM1 ARHGDIA TBCD FN3K METRNL B3GNTL1 SIRT7 LOC105376790 GPS1 RFNG C17orf62 PPP1R27 NPB PCYT2 ANAPC11 TEX19 HEXDC FN3KRP SNORD134 WDR45B P4HB SLC16A3 CD7

Back To Top

More Information


Additional Information:

For this assay, SNP(s) [rs117547546] 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)


Back To Top

Related Products