no abnormal phenotype detected_Avp<tm2Lja>/Avp<tm2Lja>

http://metadb.riken.jp/0002169I129S1Sv129X1SvJAvptm2LjaAvptm2LjaAvptm2Lja

no abnormal phenotype detected_Avp<tm2Lja>/Avp<tm2Lja>

表現型アノテーション

MGI marker

http://metadb.riken.jp/db/mgi_rdf/variant_of

• arginine vasopressin
  http://metadb.riken.jp/db/mgi_rdf/MGI:88121

遺伝子型

http://metadb.riken.jp/db/mgi_rdf/allele_composition

• Avp<tm2Lja>/Avp<tm2Lja>

アレルシンボル

http://metadb.riken.jp/db/mgi_rdf/allele_symbol

• Avp<tm2Lja>

遺伝的背景

http://metadb.riken.jp/db/mgi_rdf/genetic_background

• involves: 129S1/Sv * 129X1/SvJ

MP annotation

http://metadb.riken.jp/db/bioresource_schema/brs_indicatesPhenotype

• no abnormal phenotype detected
  http://purl.obolibrary.org/obo/MP_0002169

文献

http://purl.org/net/cito/citesAsAuthority

• Theron A. Russell, et.al., A murine model of autosomal dominant neurohypophyseal diabetes insipidus reveals progressive loss of vasopressin-producing neurons., The Journal of clinical investigation, 2003, 112
  http://rdf.ncbi.nlm.nih.gov/pubmed/14660745