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

Chr.17:81686321 on build GRCh38
Cytoband
17q25.3
Assay ID Hs02141752_cn
Size
Availability Made To Order
Catalog # 4400291
Price 457.00
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Assay Details

Target Gene Details

Entrez Gene ID:

 9146

Gene Name:

 hepatocyte growth factor-regulated tyrosine kinase substrate

Gene Aliases:

 HRS

Location:

 Chr.17:81683932-81702121 on Build GRCh38

Assay Gene Location:

 Overlaps Intron 3 - Exon 4
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
HGS NM_004712.4 NP_004703.1
XM_011525463.2 XP_011523765.1
XM_017025297.1 XP_016880786.1
XM_017025298.1 XP_016880787.1
AF260566.1 AAF82361.1
AK294190.1
AK303800.1
BC003565.1 AAH03565.1
BT009754.1 AAP88756.1
D84064.1 BAA23366.1
DR001213.1
KU178466.1
KU178467.1
U43895.1 AAC51929.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
esv26223 Chr.17:80659041 - 81736487 on Build GRCh38 Gain+Loss TEPSIN BAIAP2 LOC100129503 MIR4740 BAIAP2-AS1 PDE6G NPLOC4 LOC101928855 MIR6786 RPTOR C17orf89 LOC400627 MRPL12 LOC107985022 MIR657 MIR338 LOC105371925 AATK-AS1 MIR3186 BAHCC1 CHMP6 FAAP100 LINC00482 TSPAN10 FSCN2 CCDC137 ARL16 AATK SLC25A10 ACTG1 MIR1250 LOC105371921 MIR3065 LOC100130370 CEP131 SLC38A10 OXLD1 HGS LOC107985021 TMEM105
nsv428351 Chr.17:81152631 - 83064073 on Build GRCh38 Gain SLC16A3 SNORD134 LOC105376790 CD7 LOC105371944 C17orf89 LOC101929552 ASPSCR1 FASN MIR6787 LOC101929511 ANAPC11 MIR4525 B3GNTL1 LRRC45 FAAP100 UTS2R LINC00482 TSPAN10 GPS1 ARL16 NOTUM DCXR RFNG PPP1R27 FN3K MAFG-AS1 HGS GCGR CCDC57 NARF TEPSIN C17orf62 CSNK1D MCRIP1 MIR4740 MYADML2 ALYREF PDE6G NPLOC4 MIR6786 ZNF750 HEXDC ARHGDIA MRPL12 MAFG WDR45B SECTM1 RAB40B LOC105371925 LOC105376791 STRA13 AATK-AS1 MIR3186 BAHCC1 FN3KRP PCYT2 FSCN2 CCDC137 AATK RAC3 SLC25A10 FOXK2 ACTG1 TEX19 PYCR1 OGFOD3 TBCD LOC100130370 SIRT7 CEP131 SLC38A10 OXLD1 P4HB DUS1L NPB TMEM105
nsv470620 Chr.17:81516973 - 82064485 on Build GRCh38 Loss MCRIP1 MYADML2 ALYREF PDE6G NPLOC4 MIR6786 ARHGDIA MRPL12 MAFG ASPSCR1 STRA13 ANAPC11 LRRC45 PCYT2 FAAP100 TSPAN10 FSCN2 CCDC137 GPS1 ARL16 RAC3 SLC25A10 PYCR1 NOTUM DCXR RFNG PPP1R27 SIRT7 OXLD1 MAFG-AS1 HGS P4HB GCGR DUS1L NPB
nsv952390 Chr.17:81637175 - 81860124 on Build GRCh38 Deletion TSPAN10 MCRIP1 CCDC137 ARL16 PDE6G SLC25A10 MIR6786 PPP1R27 MRPL12 OXLD1 HGS P4HB GCGR

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More Information


Additional Information:

For this assay, SNP(s) [rs72858892,rs72858893] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Set Membership:

 Intragenic Non-exonic DGV Variation

Gene Ontology Categories:

Function(s) Process(es)


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