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

Chr.11:497018 on build GRCh38
Cytoband
11p15.5
Assay ID Hs03792056_cn
Size
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:

 Within Intron 12
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_011520259.2 XP_011518561.1
XM_011520260.2 XP_011518562.1
XM_011520261.2 XP_011518563.1
XM_011520262.2 XP_011518564.1
XM_011520263.1 XP_011518565.1
XM_017018106.1 XP_016873595.1
AB209196.1 BAD92433.1
AK027172.1 BAB15684.1
AK311379.1
AL161967.1 CAB82310.1
BC000677.2 AAH00677.1
BC003506.1 AAH03506.1
BC011186.1 AAH11186.1
BC011500.1 AAH11500.1
BC014629.2 AAH14629.1
BC024037.1 AAH24037.1
BC047730.1 AAH47730.1
BQ650217.1
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 IFITM2 ANO9 RNH1 LOC143666 PGGHG PTDSS2 IFITM5 SIGIRR LRRC56 IFITM1 PKP3 IFITM3 IRF7 MIR210HG MIR210 B4GALNT4 HRAS LMNTD2 CDHR5 LOC101059906 PHRF1 RASSF7
nsv469923 Chr.11:378188 - 1302334 on Build GRCh38 Loss PIDD1 TSPAN4 AP2A2 MIR6744 MUC5AC PTDSS2 PNPLA2 POLR2L LOC101927503 SIGIRR LRRC56 SCT TALDO1 TMEM80 CEND1 PKP3 MUC2 SLC25A22 MIR210HG B4GALNT4 CRACR2B HRAS PDDC1 DEAF1 RASSF7 CHID1 MUC6 LOC171391 MUC5B ANO9 RNH1 LOC143666 DRD4 EPS8L2 TOLLIP CD151 SNORA52 IRF7 RPLP2 MIR210 PANO1 LMNTD2 CDHR5 LOC101059906 PHRF1
esv2759794 Chr.11:409846 - 1336162 on Build GRCh38 Loss PIDD1 TSPAN4 AP2A2 MIR6744 MUC5AC PTDSS2 PNPLA2 POLR2L LOC101927503 SIGIRR LRRC56 SCT TALDO1 TMEM80 CEND1 MUC2 SLC25A22 MIR210HG CRACR2B HRAS PDDC1 DEAF1 RASSF7 CHID1 MUC6 LOC171391 MUC5B ANO9 RNH1 LOC143666 DRD4 EPS8L2 TOLLIP CD151 SNORA52 IRF7 TOLLIP-AS1 RPLP2 MIR210 PANO1 LMNTD2 CDHR5 LOC101059906 PHRF1
nsv951268 Chr.11:368601 - 503700 on Build GRCh38 Deletion PKP3 ANO9 RNH1 B4GALNT4 PTDSS2 SIGIRR
nsv1053964 Chr.11:491334 - 692433 on Build GRCh38 Gain RNH1 LOC143666 DRD4 PTDSS2 LRRC56 SCT IRF7 MIR210HG MIR210 HRAS LMNTD2 CDHR5 DEAF1 LOC101059906 PHRF1 RASSF7
dgv182e199 Chr.11:349830 - 943372 on Build GRCh38 Deletion PIDD1 TSPAN4 AP2A2 PTDSS2 PNPLA2 POLR2L SIGIRR LRRC56 SCT TALDO1 TMEM80 CEND1 PKP3 SLC25A22 MIR210HG B4GALNT4 CRACR2B HRAS PDDC1 DEAF1 RASSF7 CHID1 LOC171391 ANO9 RNH1 LOC143666 DRD4 EPS8L2 CD151 SNORA52 IRF7 RPLP2 MIR210 PANO1 LMNTD2 CDHR5 LOC101059906 PHRF1
nsv1159791 Chr.11:461793 - 909492 on Build GRCh38 Deletion PIDD1 TSPAN4 PTDSS2 PNPLA2 POLR2L LRRC56 SCT TALDO1 TMEM80 CEND1 SLC25A22 MIR210HG CRACR2B HRAS PDDC1 DEAF1 RASSF7 CHID1 LOC171391 RNH1 LOC143666 DRD4 EPS8L2 CD151 SNORA52 IRF7 RPLP2 MIR210 PANO1 LMNTD2 CDHR5 LOC101059906 PHRF1

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More Information


Additional Information:

For this assay, SNP(s) [rs72851130] 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 Intronic Non-exonic DGV Variation

Gene Ontology Categories:

Function(s) Process(es)


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