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

Chr.17:81671809 on build GRCh38
Cytoband
17q25.3
Assay ID Hs03982060_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 Exon 6 - Intron 6
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
CCDC137 NM_199287.2 NP_954981.1
XM_011524738.2 XP_011523040.1
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 CEP131 LOC100129503 MIR1250 MIR6786 LOC400627 AATK LOC107985022 MRPL12 LOC101928855 HGS CHMP6 TSPAN10 MIR3065 MIR657 MIR338 PDE6G SLC25A10 AATK-AS1 LOC107985021 SLC38A10 LOC105371921 OXLD1 BAIAP2-AS1 TEPSIN BAHCC1 NPLOC4 TMEM105 LOC105371925 ARL16 FSCN2 LOC100130370 MIR3186 LINC00482 BAIAP2 C17orf89 CCDC137 RPTOR MIR4740 FAAP100
nsv428351 Chr.17:81152631 - 83064073 on Build GRCh38 Gain ACTG1 P4HB MIR6786 LRRC45 MRPL12 CCDC57 DUS1L FN3KRP SIRT7 FASN LOC105376791 PDE6G SLC25A10 OGFOD3 MYADML2 AATK-AS1 LOC101929511 SLC38A10 B3GNTL1 MAFG PYCR1 MCRIP1 FOXK2 OXLD1 TEPSIN SNORD134 NPLOC4 TMEM105 GCGR ARL16 FSCN2 MIR3186 SECTM1 ZNF750 SLC16A3 MIR4740 RAB40B FAAP100 CEP131 NOTUM LOC101929552 AATK C17orf62 LOC105376790 RFNG HEXDC NPB TEX19 HGS TSPAN10 WDR45B ASPSCR1 LOC105371944 CSNK1D STRA13 GPS1 ALYREF MIR6787 FN3K CD7 TBCD PCYT2 UTS2R BAHCC1 MIR4525 PPP1R27 RAC3 LOC105371925 ARHGDIA LOC100130370 DCXR MAFG-AS1 NARF LINC00482 C17orf89 CCDC137 ANAPC11
nsv470620 Chr.17:81516973 - 82064485 on Build GRCh38 Loss P4HB NOTUM MIR6786 LRRC45 MRPL12 RFNG DUS1L NPB HGS SIRT7 TSPAN10 PDE6G ASPSCR1 SLC25A10 MYADML2 STRA13 MAFG PYCR1 MCRIP1 OXLD1 GPS1 ALYREF PCYT2 NPLOC4 GCGR PPP1R27 RAC3 ARHGDIA ARL16 FSCN2 DCXR MAFG-AS1 CCDC137 ANAPC11 FAAP100
nsv952390 Chr.17:81637175 - 81860124 on Build GRCh38 Deletion P4HB MIR6786 MCRIP1 OXLD1 MRPL12 HGS TSPAN10 GCGR PPP1R27 ARL16 PDE6G SLC25A10 CCDC137

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More Information


Set Membership:

 Intragenic Non-exonic DGV Variation

Gene Ontology Categories:

Process(es)


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