no abnormal phenotype detected_Slc35f1<tm1a(KOMP)Wtsi>/Slc35f1<tm1a(KOMP)Wtsi>

http://metadb.riken.jp/0002169IC57BL6C57BL6NSlc35f1tm1aKOMPWtsiSlc35f1tm1aKOMPWtsiSlc35f1tm1aKOMPWtsi

no abnormal phenotype detected_Slc35f1<tm1a(KOMP)Wtsi>/Slc35f1<tm1a(KOMP)Wtsi>

表現型アノテーション

MGI marker

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

• solute carrier family 35, member F1
  http://metadb.riken.jp/db/mgi_rdf/MGI:2139810

遺伝子型

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

• Slc35f1<tm1a(KOMP)Wtsi>/Slc35f1<tm1a(KOMP)Wtsi>

アレルシンボル

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

• Slc35f1<tm1a(KOMP)Wtsi>

遺伝的背景

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

• involves: C57BL/6 * C57BL/6N

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

• Hibret A. Adissu, et.al., Histopathology reveals correlative and unique phenotypes in a high-throughput mouse phenotyping screen., Disease models & mechanisms, 2014, 7
  http://rdf.ncbi.nlm.nih.gov/pubmed/24652767