small spleen_Fnip1<tm1.2Baba>/Fnip1<tm1.2Baba>

http://metadb.riken.jp/0000692IC57BL6C57BL6JFVBNSJLFnip1tm12BabaFnip1tm12BabaFnip1tm12Baba

small spleen_Fnip1<tm1.2Baba>/Fnip1<tm1.2Baba>

表現型アノテーション

MGI marker

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

• folliculin interacting protein 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:2444668

遺伝子型

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

• Fnip1<tm1.2Baba>/Fnip1<tm1.2Baba>

アレルシンボル

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

• Fnip1<tm1.2Baba>

遺伝的背景

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

• involves: C57BL/6 * C57BL/6J * FVB/N * SJL

MP annotation

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

• small spleen
  http://purl.obolibrary.org/obo/MP_0000692

文献

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

• Masaya. Baba, et.al., The folliculin-FNIP1 pathway deleted in human Birt-Hogg-Dubé syndrome is required for murine B-cell development., Blood, 2012, 120
  http://rdf.ncbi.nlm.nih.gov/pubmed/22709692