This product has been added to your favorites list. Go to My Favorites

Please enter the information below and press OK to send your cart to Core Services for purchase.

    

System Message

OKCancel
LOADING ...
  • Home
  • › Search Tool
  • › Search Results
  • › Hs00359903_cn
See other RENBP CNV Assays ›
Gene Symbol
RENBP
Assay Reference Genome
Location

Chr.X:153941624 on build GRCh38
Cytoband
Xq28
Assay ID Hs00359903_cn
Size
Availability Made To Order
Catalog # 4400291
Price 4,505.00
Your Price
Online offer:
4505.0
Check your price ›
  • Genomic Map
  • Assay Details
  • More Information

Genomic Map

LOADING...
×
Back To Top

Assay Details

Target Gene Details

Entrez Gene ID:

5973

Gene Name:

renin binding protein

Gene Aliases:

RBP, RNBP

Location:

Chr.X:153935263-153944780 on Build GRCh38

Assay Gene Location:

Overlaps Intron 7 - Exon 8
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
RENBP NM_002910.5 NP_002901.2
XM_017029698.1 XP_016885187.1
AK298125.1
BC015558.2 AAH15558.1
D10232.1 BAA01082.1

Target Copy Number Variation Details

DGV Version:

Release date: 2016-05-15, GRCh GRCh38
Target
Variation
Location CNV
Subtype
Genes
esv33199 Chr.X:153065734 - 154591978 on Build GRCh38 Gain+Loss TKTL1 HAUS7 BGN OPN1MW LAGE3 PNCK CTAG1A MAGEA1 SRPK3 TEX28 SLC10A3 ZFP92 SLC6A8 G6PD LOC105373386 HCFC1-AS1 PLXNB3 BCAP31 CH17-340M24.3 MIR6858 ZNF275 DNASE1L1 ARHGAP4 LOC105373381 OPN1MW3 LCA10 LOC105373377 FAM50A OPN1LW FAM223A LOC107983954 EMD TAZ FLNA ABCD1 L1CAM IDH3G OPN1MW2 GDI1 SNORA70 NAA10 DUSP9 ATP2B3 FAM58A TREX2 IKBKG PLXNA3 SSR4 LOC107987332 MIR3202-1 MECP2 AVPR2 RPL10 PDZD4 MIR718 HCFC1 ATP6AP1 IRAK1 FAM3A MIR3202-2 LOC105373383 UBL4A TMEM187 RENBP LOC105373378 PNMA6A
nsv469867 Chr.X:153813281 - 154018926 on Build GRCh38 Loss ARHGAP4 LCA10 PDZD4 HCFC1 IRAK1 MIR3202-2 L1CAM MIR3202-1 TMEM187 HCFC1-AS1 NAA10 RENBP AVPR2

Back To Top

More Information


Additional Information:

For this assay, SNP(s) [rs78377269] 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

Panther Classification:

Molecular Function -

epimerase/racemase isomerase metabolite interconversion enzyme

Gene Ontology Categories:

Function(s) Process(es)

N-acetylglucosamine metabolic process
UDP-N-acetylglucosamine biosynthetic process
N-acetylmannosamine metabolic process
regulation of blood pressure
negative regulation of endopeptidase activity
N-acetylneuraminate catabolic process
endopeptidase inhibitor activity
ATP binding
protein homodimerization activity
N-acylglucosamine 2-epimerase activity

Back To Top

Related Products

  • TaqMan® Genotyping Master Mix
  • TaqPath®ProAmp® Master Mix
  • TaqMan® Universal Master Mix II, no UNG
  • TaqMan® Gene Expression Master Mix
  • TaqMan® Universal PCR Master Mix
  • TaqMan® Universal PCR Master Mix, No AmpErase UNG

Your items have has been added!


Host server : magellan-search-green-659f68c6f4-l4hk6:80/100.66.76.55:80.
git-commit: 208ebf2ce40f07c29af7b8d1bec64c518c8c0cf8
git-url: https://github.com/thermofisher/magellan-search
git-branch: release/2.43.0-2026.01.05-1.0