malocclusion_Npr2<pwe>/Npr2<pwe>

http://metadb.riken.jp/0000120IC3HHeJC57BL6NAWWINpr2pweNpr2pweNpr2pwe

malocclusion_Npr2<pwe>/Npr2<pwe>

表現型アノテーション

MGI marker

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

• natriuretic peptide receptor 2
  http://metadb.riken.jp/db/mgi_rdf/MGI:97372

遺伝子型

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

• Npr2<pwe>/Npr2<pwe>

アレルシンボル

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

• Npr2<pwe>

遺伝的背景

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

• involves: C3H/HeJ * C57BL/6 * NAW/WI

MP annotation

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

• malocclusion
  http://purl.obolibrary.org/obo/MP_0000120

文献

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

• Krista A. Geister, et.al., A novel loss-of-function mutation in Npr2 clarifies primary role in female reproduction and reveals a potential therapy for acromesomelic dysplasia, Maroteaux type., Human molecular genetics, 2013, 22
  http://rdf.ncbi.nlm.nih.gov/pubmed/23065701