abnormal cranium morphology_Fgfr3<tm1Llm>/Fgfr3<+>

http://metadb.riken.jp/0000438I129S2SvPasC57BL6JFgfr3tm1LlmFgfr3Fgfr3tm1LlmFgfr3

abnormal cranium morphology_Fgfr3<tm1Llm>/Fgfr3<+>

表現型アノテーション

MGI marker

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

• fibroblast growth factor receptor 3
  http://metadb.riken.jp/db/mgi_rdf/MGI:95524

遺伝子型

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

• Fgfr3<tm1Llm>/Fgfr3<+>

アレルシンボル

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

• Fgfr3<tm1Llm>|Fgfr3<+>

遺伝的背景

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

• involves: 129S2/SvPas * C57BL/6J

MP annotation

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

• abnormal cranium morphology
  http://purl.obolibrary.org/obo/MP_0000438

文献

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

• Stéphanie. Pannier, et.al., Activating Fgfr3 Y367C mutation causes hearing loss and inner ear defect in a mouse model of chondrodysplasia., Biochimica et biophysica acta, 2009, 1792
  http://rdf.ncbi.nlm.nih.gov/pubmed/19073250