abnormal styloid process morphology_Nog<tm1Amc>/Nog<+>

http://metadb.riken.jp/0008023D1129S1Nogtm1AmcNogtm1AmcNogNogtm1AmcNog

abnormal styloid process morphology_Nog<tm1Amc>/Nog<+>

表現型アノテーション

MGI marker

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

• noggin
  http://metadb.riken.jp/db/mgi_rdf/MGI:104327

遺伝子型

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

• Nog<tm1Amc>/Nog<+>

アレルシンボル

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

• Nog<tm1Amc>|Nog<+>

遺伝的背景

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

• D1.129S1-Nog<tm1Amc>

MP annotation

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

• abnormal styloid process morphology
  http://purl.obolibrary.org/obo/MP_0008023

文献

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

• Chan-Ho. Hwang, et.al., Noggin heterozygous mice: an animal model for congenital conductive hearing loss in humans., Human molecular genetics, 2008, 17
  http://rdf.ncbi.nlm.nih.gov/pubmed/18096605