no abnormal phenotype detected_Ocrl<tm1Nbm>/Ocrl<tm1Nbm>

http://metadb.riken.jp/0002169EI129SSvEvC57BL6orI129SSvEvNIHBlackSwissOcrltm1NbmOcrltm1NbmOcrltm1Nbm

no abnormal phenotype detected_Ocrl<tm1Nbm>/Ocrl<tm1Nbm>

表現型アノテーション

MGI marker

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

• OCRL, inositol polyphosphate-5-phosphatase
  http://metadb.riken.jp/db/mgi_rdf/MGI:109589

遺伝子型

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

• Ocrl<tm1Nbm>/Ocrl<tm1Nbm>

アレルシンボル

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

• Ocrl<tm1Nbm>

遺伝的背景

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

• either: (involves: 129S/SvEv * C57BL/6) or (involves: 129S/SvEv * NIH Black Swiss)

MP annotation

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

• no abnormal phenotype detected
  http://purl.obolibrary.org/obo/MP_0002169

文献

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

• P A. Jänne, et.al., Functional overlap between murine Inpp5b and Ocrl1 may explain why deficiency of the murine ortholog for OCRL1 does not cause Lowe syndrome in mice., The Journal of clinical investigation, 1998, 101
  http://rdf.ncbi.nlm.nih.gov/pubmed/9593760