abnormal stationary movement_Aff1<Rob>/Aff1<+>

http://metadb.riken.jp/0001388IBALBcAnNCrlC3HHeNAff1RobAff1Aff1Aff1Rob

abnormal stationary movement_Aff1<Rob>/Aff1<+>

表現型アノテーション

MGI marker

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

• AF4/FMR2 family, member 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:1100819

遺伝子型

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

• Aff1<Rob>/Aff1<+>

アレルシンボル

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

• Aff1<+>|Aff1<Rob>

遺伝的背景

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

• involves: BALB/cAnNCrl * C3H/HeN

MP annotation

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

• abnormal stationary movement
  http://purl.obolibrary.org/obo/MP_0001388

文献

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

• P M. Nolan, et.al., A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse., Nature genetics, 2000, 25
  http://rdf.ncbi.nlm.nih.gov/pubmed/10932191