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NPR2

In today's article, we will explore the topic of NPR2 in depth, analyzing its importance in different contexts and its relevance in today's society. From its origins to its evolution over time, NPR2 has been the subject of study and debate, influencing thought and popular culture. Through an exhaustive analysis, we will address the different aspects that make up NPR2, examining its impact on various areas of daily life. With data, studies and relevant information, we aim to offer a comprehensive view on NPR2, providing our readers with an enriching and novel perspective on this topic.

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NPR2
Identifiers
AliasesNPR2, AMDM, ANPRB, ANPb, ECDM, GUC2B, GUCY2B, NPRB, NPRBi, SNSK, natriuretic peptide receptor 2, GCB, AMD1, GC-B
External IDsOMIM: 108961; MGI: 97372; HomoloGene: 2970; GeneCards: NPR2; OMA:NPR2 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_000907
NM_003995
NM_001378923

NM_173788
NM_001355466

RefSeq (protein)

NP_003986
NP_001365852

NP_776149
NP_001342395

Location (UCSC)Chr 9: 35.79 – 35.81 MbChr 4: 43.63 – 43.65 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Natriuretic peptide receptor B (NPR2), also known as atrionatriuretic peptide receptor B and formerly as guanylate cyclase B, is an atrial natriuretic peptide receptor which in humans is encoded by the NPR2 gene.[5]

A mutation in the NPR2 gene can result in achondroplasia and disproportionate dwarfism with short limbs.[6]

See also

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000159899Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000028469Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ "Entrez Gene: NPR2 natriuretic peptide receptor B/guanylate cyclase B (atrionatriuretic peptide receptor B)".
  6. ^ Tsuji T, Kunieda T (April 2005). "A loss-of-function mutation in natriuretic peptide receptor 2 (Npr2) gene is responsible for disproportionate dwarfism in cn/cn mouse". The Journal of Biological Chemistry. 280 (14): 14288–92. doi:10.1074/jbc.C500024200. PMID 15722353.

Further reading

This article incorporates text from the United States National Library of Medicine, which is in the public domain.