cpath:CPATH-118361 | rdf:type | http://www.biopax.org/relea... | lld:biogrid |
cpath:CPATH-118361 | http://www.biopax.org/relea... | cpath:CPATH-LOCAL-487716 | lld:biogrid |
cpath:CPATH-118361 | http://www.biopax.org/relea... | cpath:CPATH-LOCAL-487717 | lld:biogrid |
cpath:CPATH-118361 | http://www.biopax.org/relea... | cpath:CPATH-LOCAL-487718 | lld:biogrid |
cpath:CPATH-118361 | http://www.biopax.org/relea... | cpath:CPATH-LOCAL-487719 | lld:biogrid |
cpath:CPATH-118361 | http://www.biopax.org/relea... | cpath:CPATH-LOCAL-487720 | lld:biogrid |
cpath:CPATH-118361 | http://www.biopax.org/relea... | cpath:CPATH-LOCAL-487721 | lld:biogrid |
cpath:CPATH-118361 | http://www.biopax.org/relea... | cpath:CPATH-LOCAL-491650 | lld:biogrid |
cpath:CPATH-118361 | http://www.biopax.org/relea... | Vasopressin-neurophysin 2-copeptin | lld:biogrid |
cpath:CPATH-118361 | http://www.biopax.org/relea... | NEU2_HUMAN | lld:biogrid |
cpath:CPATH-118361 | http://www.biopax.org/relea... | cpath:CPATH-LOCAL-487714 | lld:biogrid |
cpath:CPATH-118361 | http://www.biopax.org/relea... | AVP-NPII | lld:biogrid |
cpath:CPATH-118361 | http://www.biopax.org/relea... | Copeptin | lld:biogrid |
cpath:CPATH-118361 | http://www.biopax.org/relea... | Neurophysin 2 | lld:biogrid |
cpath:CPATH-118361 | http://www.biopax.org/relea... | Arg-vasopressin | lld:biogrid |
cpath:CPATH-118361 | http://www.biopax.org/relea... | Neurophysin-II | lld:biogrid |
cpath:CPATH-118361 | http://www.biopax.org/relea... | FUNCTION: Neurophysin 2 specifically binds vasopressin. FUNCTION: Vasopressin has a direct antidiuretic action on the kidney, it also causes vasoconstriction of the peripheral vessels. SUBCELLULAR LOCATION: Secreted. DISEASE: Defects in AVP are the cause of autosomal dominant neurohypophyseal diabetes insipidus (ADNDI) [MIM:125700]. ADNDI is characterized by persistent thirst, polydipsia and polyuria. The disease is transmitted in an autosomal dominant mode and appears to be largely if not completely penetrant. DISEASE: Defects in AVP are the cause of autosomal recessive neurohypophyseal diabetes insipidus (ARNDI) [MIM:125700]. ARNDI is characterized by persistent thirst, polydipsia and polyuria. Most mutations are hypothesized to trigger neurodegeneration via disruption of preproAVP-NPII processing. SIMILARITY: Belongs to the vasopressin/oxytocin family. WEB RESOURCE: Name=GeneReviews; URL="http://www.ncbi.nlm.nih.gov/sites/GeneTests/lab/gene/AVP"; WEB RESOURCE: Name=Wikipedia; Note=Vasopressin entry; URL="http://en.wikipedia.org/wiki/Vasopressin"; GENE SYNONYMS: ARVP VP. COPYRIGHT: Protein annotation is derived from the UniProt Consortium (http://www.uniprot.org/). Distributed under the Creative Commons Attribution-NoDerivs License. | lld:biogrid |
cpath:CPATH-118361 | skos:exactMatch | uniprot-protein:P01185 | lld:mappings |
cpath:CPATH-118361 | skos:closeMatch | entrez-gene:551 | lld:mappings |
cpath:CPATH-LOCAL-11547984 | http://www.biopax.org/relea... | cpath:CPATH-118361 | lld:biogrid |
cpath:CPATH-LOCAL-11649309 | http://www.biopax.org/relea... | cpath:CPATH-118361 | lld:biogrid |