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See other CCDC137 CNV Assays ›
Gene Symbol
CCDC137
Assay Reference Genome
Location

Chr.17:81667177 on build GRCh38
Cytoband
17q25.3
Assay ID Hs03954751_cn
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Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 339230

Gene Name:

 coiled-coil domain containing 137

Gene Aliases:

 RaRF

Location:

 Chr.17:81666697-81673907 on Build GRCh38

Assay Gene Location:

 Within Intron 2
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
CCDC137 NM_199287.2 NP_954981.1
XM_011524738.2 XP_011523040.1
XM_017024573.1 XP_016880062.1
BC009369.2 AAH09369.1
BM548065.1
FJ649645.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv828128 Chr.17:80659041 - 81736487 on Build GRCh38 Loss ACTG1 LOC400627 MIR657 SLC38A10 MIR1250 LOC101928855 LINC00482 AATK-AS1 MRPL12 MIR3065 PDE6G NPLOC4 CCDC137 LOC100130370 LOC105371925 TEPSIN BAIAP2-AS1 OXLD1 LOC107985021 AATK MIR6786 SLC25A10 BAIAP2 HGS LOC107985022 LOC100129503 MIR4740 LOC105371921 RPTOR ARL16 BAHCC1 FAAP100 TMEM105 TSPAN10 MIR338 CHMP6 MIR3186 CEP131 FSCN2 C17orf89
nsv428351 Chr.17:81152631 - 83064073 on Build GRCh38 Gain ARHGDIA DUS1L SECTM1 ASPSCR1 MYADML2 OGFOD3 RAB40B MIR6787 AATK-AS1 MRPL12 CSNK1D FASN GCGR LRRC45 LOC105371925 TEPSIN NPB STRA13 PYCR1 PCYT2 ZNF750 MAFG SLC16A3 CCDC57 RFNG RAC3 LOC101929552 FN3K SLC25A10 FOXK2 TBCD MAFG-AS1 TEX19 LOC101929511 LOC105371944 NARF BAHCC1 P4HB UTS2R C17orf62 PPP1R27 CD7 TSPAN10 MIR3186 NOTUM ALYREF ANAPC11 ACTG1 GPS1 SLC38A10 LOC105376791 SNORD134 LINC00482 MIR4525 B3GNTL1 HEXDC PDE6G NPLOC4 CCDC137 LOC100130370 DCXR FN3KRP WDR45B LOC105376790 SIRT7 OXLD1 AATK MIR6786 MCRIP1 HGS MIR4740 ARL16 FAAP100 TMEM105 CEP131 FSCN2 C17orf89
nsv470620 Chr.17:81516973 - 82064485 on Build GRCh38 Loss ARHGDIA ALYREF ANAPC11 DUS1L ASPSCR1 GPS1 MYADML2 MRPL12 PDE6G NPLOC4 GCGR CCDC137 LRRC45 DCXR NPB STRA13 PYCR1 PCYT2 SIRT7 MAFG OXLD1 MIR6786 RFNG RAC3 SLC25A10 MCRIP1 HGS MAFG-AS1 ARL16 FAAP100 P4HB PPP1R27 TSPAN10 NOTUM FSCN2
nsv952390 Chr.17:81637175 - 81860124 on Build GRCh38 Deletion OXLD1 MIR6786 SLC25A10 MCRIP1 HGS MRPL12 PDE6G ARL16 P4HB PPP1R27 GCGR TSPAN10 CCDC137

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More Information


Set Membership:

 Intragenic Intronic Non-exonic DGV Variation

Gene Ontology Categories:

Process(es)


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