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See other RNH1 CNV Assays ›
Gene Symbol
RNH1
Assay Reference Genome
Location

Chr.11:504968 on build GRCh38
Cytoband
11p15.5
Assay ID Hs01846004_cn
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Availability Made To Order
Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 6050

Gene Name:

 ribonuclease/angiogenin inhibitor 1

Gene Aliases:

 RAI, RNH

Location:

 Chr.11:494512-507283 on Build GRCh38

Assay Gene Location:

 Overlaps Intron 3 - Exon 4
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
RNH1 NM_002939.3 NP_002930.2
NM_203383.1 NP_976317.1
NM_203384.1 NP_976318.1
NM_203385.1 NP_976319.1
NM_203386.2 NP_976320.1
NM_203387.2 NP_976321.1
NM_203388.2 NP_976322.1
NM_203389.2 NP_976323.1
XM_011520255.1 XP_011518557.1
XM_011520257.2 XP_011518559.1
XM_011520258.2 XP_011518560.1
XM_011520260.2 XP_011518562.1
XM_011520261.2 XP_011518563.1
XM_011520262.2 XP_011518564.1
XM_017018106.1 XP_016873595.1
AB209196.1 1 914 BAD92433.1
AK308340.1
AK310173.1
AK311379.1
AL534410.3
AL539148.3
BC000677.2 AAH00677.1
BC003506.1 AAH03506.1
BC011500.1 AAH11500.1
BC014629.2 AAH14629.1
BC024037.1 AAH24037.1
BC047730.1 AAH47730.1
BG716555.1
BG720935.1
BG752774.1
BM019570.1
BM465975.1
BM562998.1
BQ927358.1
BQ954409.1
DC296330.1
M22414.1 AAA59130.1
M36717.1 AAA60249.1
X13973.1 CAA32151.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv527327 Chr.11:295343 - 620599 on Build GRCh38 Loss LOC101059906 CDHR5 IFITM3 LOC143666 B4GALNT4 LMNTD2 IFITM1 IRF7 ANO9 SIGIRR MIR210HG PTDSS2 MIR210 PHRF1 HRAS LRRC56 RNH1 IFITM5 PKP3 PGGHG IFITM2 RASSF7
nsv469923 Chr.11:378188 - 1302334 on Build GRCh38 Loss PNPLA2 TALDO1 CDHR5 LOC101927503 CHID1 DEAF1 PDDC1 ANO9 CD151 TMEM80 MIR210HG PTDSS2 MUC6 MIR210 PHRF1 HRAS LRRC56 CRACR2B SCT EPS8L2 MUC5AC LOC171391 PIDD1 LOC101059906 MUC5B TOLLIP LOC143666 B4GALNT4 LMNTD2 IRF7 MIR6744 DRD4 AP2A2 SIGIRR RPLP2 SLC25A22 MUC2 POLR2L TSPAN4 PANO1 SNORA52 CEND1 RNH1 PKP3 RASSF7
esv2759794 Chr.11:409846 - 1336162 on Build GRCh38 Loss TOLLIP-AS1 PNPLA2 TALDO1 CDHR5 LOC101927503 CHID1 DEAF1 PDDC1 ANO9 CD151 TMEM80 MIR210HG PTDSS2 MUC6 MIR210 PHRF1 HRAS LRRC56 CRACR2B SCT EPS8L2 MUC5AC LOC171391 PIDD1 LOC101059906 MUC5B TOLLIP LOC143666 LMNTD2 IRF7 MIR6744 DRD4 AP2A2 SIGIRR RPLP2 SLC25A22 MUC2 POLR2L TSPAN4 PANO1 SNORA52 CEND1 RNH1 RASSF7
nsv1053964 Chr.11:491334 - 692433 on Build GRCh38 Gain LOC101059906 CDHR5 LOC143666 LMNTD2 IRF7 DRD4 DEAF1 MIR210HG PTDSS2 MIR210 PHRF1 HRAS LRRC56 SCT RNH1 RASSF7
dgv182e199 Chr.11:349830 - 943372 on Build GRCh38 Deletion PNPLA2 TALDO1 CDHR5 CHID1 DEAF1 PDDC1 ANO9 CD151 TMEM80 MIR210HG PTDSS2 MIR210 PHRF1 HRAS LRRC56 CRACR2B SCT EPS8L2 LOC171391 PIDD1 LOC101059906 LOC143666 B4GALNT4 LMNTD2 IRF7 DRD4 AP2A2 SIGIRR RPLP2 SLC25A22 POLR2L TSPAN4 PANO1 SNORA52 CEND1 RNH1 PKP3 RASSF7
nsv1159791 Chr.11:461793 - 909492 on Build GRCh38 Deletion PNPLA2 TALDO1 CDHR5 CHID1 DEAF1 PDDC1 CD151 TMEM80 MIR210HG PTDSS2 MIR210 PHRF1 HRAS LRRC56 CRACR2B SCT EPS8L2 LOC171391 PIDD1 LOC101059906 LOC143666 LMNTD2 IRF7 DRD4 RPLP2 SLC25A22 POLR2L TSPAN4 PANO1 SNORA52 CEND1 RNH1 RASSF7

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More Information


Additional Information:

For this assay, SNP(s) [rs72851192] 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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