abnormal intestine morphology_Fermt1<tm1Ref>/Fermt1<tm1Ref>

http://metadb.riken.jp/0000477I129S1Sv129X1SvJFermt1tm1RefFermt1tm1RefFermt1tm1Ref

abnormal intestine morphology_Fermt1<tm1Ref>/Fermt1<tm1Ref>

表現型アノテーション

MGI marker

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

• fermitin family member 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:2443583

遺伝子型

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

• Fermt1<tm1Ref>/Fermt1<tm1Ref>

アレルシンボル

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

• Fermt1<tm1Ref>

遺伝的背景

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

• involves: 129S1/Sv * 129X1/SvJ

MP annotation

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

• abnormal intestine morphology
  http://purl.obolibrary.org/obo/MP_0000477

文献

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

• Siegfried. Ussar, et.al., Loss of Kindlin-1 causes skin atrophy and lethal neonatal intestinal epithelial dysfunction., PLoS genetics, 2008, 4
  http://rdf.ncbi.nlm.nih.gov/pubmed/19057668