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See other C17ORF97 CNV Assays ›
Gene Symbol
C17orf97
Assay Reference Genome
Location

Chr.17:414493 on build GRCh38
Cytoband
17p13.3
Assay ID Hs00975453_cn
Size
Availability Made To Order
Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 400566

Gene Name:

 chromosome 17 open reading frame 97

Gene Aliases:

 CK20, LIAT1

Location:

 Chr.17:410327-414666 on Build GRCh38

Assay Gene Location:

 Within Exon 2
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
C17orf97 NM_001013672.4 2 1666 NP_001013694.4
BC057385.1 AAH57385.1
BC141806.1
BG056786.1 1 176
KR780251.1 2 1666

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
dgv5386n54 Chr.17:407766 - 816212 on Build GRCh38 Gain C17orf97 VPS53 DBIL5P NXN MRM3 GEMIN4 LOC105371430 GLOD4 FAM101B FAM57A
esv3639622 Chr.17:364641 - 422978 on Build GRCh38 Gain C17orf97 LOC105371430 RPH3AL
nsv827849 Chr.17:332394 - 445831 on Build GRCh38 Gain C17orf97 LOC105371430 LOC100506388 FAM101B RPH3AL
dgv3071n100 Chr.17:150721 - 853554 on Build GRCh38 Gain C17orf97 NXN DOC2B GEMIN4 GLOD4 FAM57A RPH3AL VPS53 DBIL5P LOC100506371 MRM3 LOC105371430 LOC100506388 FAM101B
esv3639624 Chr.17:370897 - 446617 on Build GRCh38 Gain C17orf97 LOC105371430 FAM101B RPH3AL
dgv3072n100 Chr.17:410957 - 881396 on Build GRCh38 Gain C17orf97 VPS53 DBIL5P NXN MRM3 GEMIN4 LOC105371430 GLOD4 FAM101B FAM57A
esv2761938 Chr.17:309346 - 424754 on Build GRCh38 Gain C17orf97 LOC105371430 LOC100506388 RPH3AL
esv2422420 Chr.17:210752 - 1113141 on Build GRCh38 Duplication MIR3183 LOC100130876 C17orf97 NXN GEMIN4 GLOD4 FAM57A RPH3AL ABR VPS53 DBIL5P LOC101927727 TIMM22 MRM3 LOC105371430 LOC100506388 FAM101B
nsv457627 Chr.17:201297 - 733582 on Build GRCh38 Gain C17orf97 VPS53 LOC105371430 LOC100506388 FAM101B FAM57A RPH3AL
esv3892944 Chr.17:368038 - 947302 on Build GRCh38 Gain LOC100130876 C17orf97 NXN GEMIN4 GLOD4 FAM57A RPH3AL VPS53 DBIL5P LOC101927727 MRM3 LOC105371430 FAM101B

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More Information


Set Membership:

 Intragenic Exonic DGV Variation

Gene Ontology Categories:

Function(s)


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