impaired hearing_Fam20c<tm1Lex>/Fam20c<tm1Lex>

http://metadb.riken.jp/0006325I129S5SvEvBrdC57BL6Fam20ctm1LexFam20ctm1LexFam20ctm1Lex

impaired hearing_Fam20c<tm1Lex>/Fam20c<tm1Lex>

表現型アノテーション

MGI marker

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

• family with sequence similarity 20, member C
  http://metadb.riken.jp/db/mgi_rdf/MGI:2136853

遺伝子型

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

• Fam20c<tm1Lex>/Fam20c<tm1Lex>

アレルシンボル

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

• Fam20c<tm1Lex>

遺伝的背景

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

• involves: 129S5/SvEvBrd * C57BL/6

MP annotation

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

• impaired hearing
  http://purl.obolibrary.org/obo/MP_0006325

文献

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

• P. Vogel, et.al., Amelogenesis imperfecta and other biomineralization defects in Fam20a and Fam20c null mice., Veterinary pathology, 2012, 49
  http://rdf.ncbi.nlm.nih.gov/pubmed/22732358