Atrial natriuretic peptide receptor 2

Summary
UniProt ID
P20594
Gene Symbol
NPR2 ANPRB
Gene ID
4882
Organism
Homo sapiens (human)
PubChem
P20594
The Human Metabolome Database
HMDBP01063
Re-Glyco
P20594
Annotation
Keyword
Alternative splicing Cell membrane Disease variant Disulfide bond Dwarfism GTP-binding Glycoprotein Lyase Osteogenesis Phosphoprotein Proteomics identification Receptor Reference proteome Signal Transmembrane helix cGMP biosynthesis
Gene Ontology (GO)
GO Hierarchy
GO Hierarchy
Sequence
MALPSLLLLVAALAGGVRPPGARNLTLAVVLPEHNLSYAWAWPRVGPAVALAVEALGRALPVDLRFVSSELEGACSEYLAPLSAVDLKLYHDPDLLLGPGCVYPAASVARFASHWRLPLLTAGAVASGFSAKNDHYRTLVRTGPSAPKLGEFVVTLHGHFNWTARAALLYLDARTDDRPHYFTIEGVFEALQGSNLSVQHQVYAREPGGPEQATHFIRANGRIVYICGPLEMLHEILLQAQRENLTNGDYVFFYLDVFGESLRAGPTRATGRPWQDNRTREQAQALREAFQTVLVITYREPPNPEYQEFQNRLLIRAREDFGVELGPSLMNLIAGCFYDGILLYAEVLNETIQEGGTREDGLRIVEKMQGRRYHGVTGLVVMDKNNDRETDFVLWAMGDLDSGDFQPAAHYSGAEKQIWWTGRPIPWVKGAPPSDNPPCAFDLDDPSCDKTPLSTLAIVALGTGITFIMFGVSSFLIFRKLMLEKELASMLWRIRWEELQFGNSERYHKGAGSRLTLSLRGSSYGSLMTAHGKYQIFANTGHFKGNVVAIKHVNKKRIELTRQVLFELKHMRDVQFNHLTRFIGACIDPPNICIVTEYCPRGSLQDILENDSINLDWMFRYSLINDLVKGMAFLHNSIISSHGSLKSSNCVVDSRFVLKITDYGLASFRSTAEPDDSHALYAKKLWTAPELLSGNPLPTTGMQKADVYSFGIILQEIALRSGPFYLEGLDLSPKEIVQKVRNGQRPYFRPSIDRTQLNEELVLLMERCWAQDPAERPDFGQIKGFIRRFNKEGGTSILDNLLLRMEQYANNLEKLVEERTQAYLEEKRKAEALLYQILPHSVAEQLKRGETVQAEAFDSVTIYFSDIVGFTALSAESTPMQVVTLLNDLYTCFDAIIDNFDVYKVETIGDAYMVVSGLPGRNGQRHAPEIARMALALLDAVSSFRIRHRPHDQLRLRIGVHTGPVCAGVVGLKMPRYCLFGDTVNTASRMESNGQALKIHVSSTTKDALDELGCFQLELRGDVEMKGKGKMRTYWLLGERKGPPGLL
Glycosylation Sites
Displaying all 7 entries
Position Description PubMed ID GlyTouCan ID Source
24
  • N-linked (GlcNAc...) asparagine
35
  • N-linked (GlcNAc...) asparagine
161
  • N-linked (GlcNAc...) asparagine
195
  • N-linked (GlcNAc...) asparagine
244
  • N-linked (GlcNAc...) asparagine
277
  • N-linked (GlcNAc...) asparagine
349
  • N-linked (GlcNAc...) asparagine
Feature
  • ProtVista GlyGen : Glycosylation Site from GlyGen
  • ProtVista UniProt : Glycosylation Site from UniProt
Pathway
Displaying 1 entry
Pathway Name Organism
Physiological factors Homo sapiens
Disease
Displaying all 3 entries
DO ID Disease Name Source
DOID:0080050 acromesomelic dysplasia, Maroteaux type
DOID:10825 essential hypertension
DOID:0070316 Miura type epiphyseal chondrodysplasia

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International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: April 6, 2026