absent enamel_Fam20a<tm1Lex>/Fam20a<tm1Lex>

http://metadb.riken.jp/0003404I129S5SvEvBrdC57BL6Fam20atm1LexFam20atm1LexFam20atm1Lex

absent enamel_Fam20a<tm1Lex>/Fam20a<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 A
  http://metadb.riken.jp/db/mgi_rdf/MGI:2388266

遺伝子型

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

• Fam20a<tm1Lex>/Fam20a<tm1Lex>

アレルシンボル

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

• Fam20a<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

• absent enamel
  http://purl.obolibrary.org/obo/MP_0003404

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