narrow eye opening_Foxp3<sf>/Y

http://metadb.riken.jp/0005287I101HC3HHeHSTOCKMRFoxp3sfYFoxp3sf

narrow eye opening_Foxp3<sf>/Y

表現型アノテーション

MGI marker

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

• forkhead box P3
  http://metadb.riken.jp/db/mgi_rdf/MGI:1891436

遺伝子型

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

• Foxp3<sf>/Y

アレルシンボル

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

• Foxp3<sf>

遺伝的背景

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

• involves: 101/H * C3H/HeH * STOCK MR

MP annotation

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

• narrow eye opening
  http://purl.obolibrary.org/obo/MP_0005287

文献

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

• M F. Lyon, et.al., The scurfy mouse mutant has previously unrecognized hematological abnormalities and resembles Wiskott-Aldrich syndrome., Proceedings of the National Academy of Sciences of the United States of America, 1990, 87
  http://rdf.ncbi.nlm.nih.gov/pubmed/2320565