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

Chr.17:81670216 on build GRCh38
Cytoband
17q25.3
Assay ID Hs03980073_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:

 Overlaps Intron 3 - Exon 4
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 CHMP6 CCDC137 LOC107985022 BAIAP2-AS1 C17orf89 PDE6G FSCN2 SLC38A10 OXLD1 TSPAN10 LOC100130370 ACTG1 HGS MIR4740 SLC25A10 TMEM105 TEPSIN LOC400627 BAHCC1 LOC105371921 LOC101928855 BAIAP2 AATK MIR1250 MRPL12 FAAP100 AATK-AS1 MIR3065 LOC107985021 MIR6786 LOC105371925 NPLOC4 LOC100129503 LINC00482 MIR3186 CEP131 RPTOR MIR338 MIR657 ARL16
nsv428351 Chr.17:81152631 - 83064073 on Build GRCh38 Gain LRRC45 C17orf89 PDE6G SLC38A10 PCYT2 LOC100130370 HGS MIR4740 SLC25A10 MYADML2 TMEM105 TEPSIN WDR45B OGFOD3 STRA13 GPS1 SLC16A3 NARF AATK FAAP100 RAB40B NPB FASN SIRT7 LOC105371925 GCGR FN3KRP LINC00482 MIR3186 B3GNTL1 LOC101929552 SECTM1 PYCR1 ARL16 CCDC137 CSNK1D ZNF750 TEX19 HEXDC SNORD134 FSCN2 CD7 OXLD1 TSPAN10 ACTG1 P4HB RAC3 NOTUM LOC105376790 BAHCC1 MIR4525 DCXR DUS1L LOC105371944 ALYREF C17orf62 MAFG-AS1 TBCD MRPL12 AATK-AS1 FOXK2 LOC101929511 ANAPC11 ASPSCR1 MIR6786 MIR6787 UTS2R NPLOC4 MAFG LOC105376791 CCDC57 CEP131 ARHGDIA FN3K PPP1R27 RFNG MCRIP1
nsv470620 Chr.17:81516973 - 82064485 on Build GRCh38 Loss CCDC137 LRRC45 PDE6G FSCN2 PCYT2 OXLD1 TSPAN10 HGS P4HB RAC3 SLC25A10 MYADML2 NOTUM DCXR STRA13 GPS1 DUS1L ALYREF MAFG-AS1 MRPL12 FAAP100 ANAPC11 NPB ASPSCR1 MIR6786 SIRT7 GCGR NPLOC4 MAFG ARHGDIA PYCR1 PPP1R27 RFNG MCRIP1 ARL16
nsv952390 Chr.17:81637175 - 81860124 on Build GRCh38 Deletion CCDC137 MRPL12 PDE6G MIR6786 GCGR OXLD1 TSPAN10 HGS P4HB SLC25A10 PPP1R27 MCRIP1 ARL16

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More Information


Set Membership:

 Intragenic Non-exonic DGV Variation

Gene Ontology Categories:

Process(es)


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