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See other C17ORF62 CNV Assays ›
Gene Symbol
C17orf62
Assay Reference Genome
Location

Chr.17:82446965 on build GRCh38
Cytoband
17q25.3
Assay ID Hs03965336_cn
Size
Availability Made To Order
Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 79415

Gene Name:

 chromosome 17 open reading frame 62

Gene Aliases:

 -

Location:

 Chr.17:82442586-82450831 on Build GRCh38

Assay Gene Location:

 Within Intron 3
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
C17orf62 NM_001033046.3 NP_001028218.1
NM_001100407.2 NP_001093877.1
NM_001100408.2 NP_001093878.1
NM_001193653.1 NP_001180582.1
NM_001193654.1 NP_001180583.1
NM_001193655.1 NP_001180584.1
NM_001193657.1 NP_001180586.1
NR_036514.1
NR_036516.1
NR_036517.1
NR_036518.1
XM_006722293.2 XP_006722356.1
XM_011523606.2 XP_011521908.1
XM_017025072.1 XP_016880561.1
XM_017025073.1 XP_016880562.1
XM_017025074.1 XP_016880563.1
XM_017025075.1 XP_016880564.1
XM_017025076.1 XP_016880565.1
XM_017025077.1 XP_016880566.1
XM_017025078.1 XP_016880567.1
AK027743.1 BAB55335.1
AK054876.1 BAB70818.1
AK056342.1 BAB71156.1
AK074950.1
AK090484.1 BAC03465.1
AK092865.1 1 1089
AK225389.1
AK309201.1
AU280357.1
BC003595.1 AAH03595.1
BC004171.2 AAH04171.1
BG338078.1
BG716477.1
BM147030.1
BM801484.1
CN260096.1
DA008508.1
DA342707.1
DA500882.1
DA663677.1
DA716299.1
DA969007.1
DB113745.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv1160502 Chr.17:82411695 - 82526070 on Build GRCh38 Deletion OGFOD3 FOXK2 C17orf62 HEXDC NARF
esv3641424 Chr.17:82434625 - 82462586 on Build GRCh38 Gain C17orf62 HEXDC NARF
nsv1062980 Chr.17:82408938 - 82687942 on Build GRCh38 Gain OGFOD3 FOXK2 C17orf62 HEXDC NARF WDR45B MIR4525 RAB40B
nsv428351 Chr.17:81152631 - 83064073 on Build GRCh38 Gain RAC3 CSNK1D DCXR B3GNTL1 DUS1L PCYT2 PDE6G FOXK2 LOC105371925 GCGR CCDC137 TBCD FSCN2 ASPSCR1 NPB CEP131 PYCR1 CD7 LOC105376790 LRRC45 MIR6787 ACTG1 LOC105376791 LOC101929552 OGFOD3 FN3KRP GPS1 TEPSIN MAFG-AS1 FAAP100 MCRIP1 NARF ARHGDIA WDR45B ANAPC11 LOC105371944 SLC16A3 TEX19 MYADML2 SLC38A10 HEXDC OXLD1 MIR4525 AATK-AS1 ZNF750 AATK STRA13 P4HB CCDC57 TSPAN10 LOC101929511 LINC00482 LOC100130370 PPP1R27 SLC25A10 RAB40B RFNG MIR6786 NOTUM TMEM105 FN3K C17orf89 MRPL12 UTS2R C17orf62 SNORD134 NPLOC4 ALYREF MIR3186 MIR4740 HGS SECTM1 MAFG BAHCC1 FASN ARL16 SIRT7
nsv469561 Chr.17:82251148 - 82472274 on Build GRCh38 Loss CSNK1D OGFOD3 SECTM1 TEX19 UTS2R CD7 C17orf62 LOC105376790 HEXDC NARF LOC101929511
nsv833574 Chr.17:82419054 - 82579254 on Build GRCh38 Gain FOXK2 C17orf62 HEXDC NARF
nsv1067194 Chr.17:82294731 - 82653129 on Build GRCh38 Gain OGFOD3 SECTM1 FOXK2 TEX19 UTS2R CD7 C17orf62 LOC105376790 HEXDC NARF WDR45B
esv2762577 Chr.17:82244836 - 82838431 on Build GRCh38 Gain+Loss LOC105376791 ZNF750 CSNK1D LOC101929552 OGFOD3 FN3KRP FN3K FOXK2 UTS2R C17orf62 NARF TBCD WDR45B LOC101929511 SECTM1 TEX19 CD7 LOC105376790 HEXDC MIR4525 RAB40B
esv21913 Chr.17:81828123 - 83103548 on Build GRCh38 Gain+Loss RAC3 CSNK1D DCXR B3GNTL1 DUS1L PCYT2 FOXK2 TBCD ASPSCR1 NPB PYCR1 CD7 LOC105376790 LRRC45 MIR6787 LOC105376791 LOC101929552 OGFOD3 FN3KRP GPS1 MAFG-AS1 MCRIP1 NARF ARHGDIA WDR45B ANAPC11 LOC105371944 SLC16A3 TEX19 MYADML2 HEXDC MIR4525 ZNF750 STRA13 METRNL P4HB CCDC57 LOC101929511 PPP1R27 RAB40B RFNG NOTUM FN3K UTS2R C17orf62 SNORD134 ALYREF SECTM1 MAFG FASN SIRT7

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More Information


Set Membership:

 Intragenic Intronic Non-exonic DGV Variation

Panther Classification:

Molecular Function -

chaperone

Gene Ontology Categories:

Process(es)


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