eyelid hypoplasia_Foxl2<tm1Gpil>/Foxl2<tm1Gpil>

http://metadb.riken.jp/0013395E129S6SvEvTacorI129S6SvEvTacC57BL6JorI129S6SvEvTacNIHSBCFoxl2tm1GpilFoxl2tm1GpilFoxl2tm1Gpil

eyelid hypoplasia_Foxl2<tm1Gpil>/Foxl2<tm1Gpil>

表現型アノテーション

MGI marker

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

• forkhead box L2
  http://metadb.riken.jp/db/mgi_rdf/MGI:1349428

遺伝子型

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

• Foxl2<tm1Gpil>/Foxl2<tm1Gpil>

アレルシンボル

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

• Foxl2<tm1Gpil>

遺伝的背景

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

• either: 129S6/SvEvTac or (involves: 129S6/SvEvTac * C57BL/6J) or (involves: 129S6/SvEvTac * NIHS-BC)

MP annotation

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

• eyelid hypoplasia
  http://purl.obolibrary.org/obo/MP_0013395

文献

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

• Manuela. Uda, et.al., Foxl2 disruption causes mouse ovarian failure by pervasive blockage of follicle development., Human molecular genetics, 2004, 13
  http://rdf.ncbi.nlm.nih.gov/pubmed/15056605