no abnormal phenotype detected_Slco1c1<tm1Arte>/Slco1c1<tm1Arte>

http://metadb.riken.jp/0002169IC57BL6Slco1c1tm1ArteSlco1c1tm1ArteSlco1c1tm1Arte

no abnormal phenotype detected_Slco1c1<tm1Arte>/Slco1c1<tm1Arte>

表現型アノテーション

MGI marker

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

• solute carrier organic anion transporter family, member 1c1
  http://metadb.riken.jp/db/mgi_rdf/MGI:1889679

遺伝子型

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

• Slco1c1<tm1Arte>/Slco1c1<tm1Arte>

アレルシンボル

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

• Slco1c1<tm1Arte>

遺伝的背景

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

• involves: C57BL/6

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

• Steffen. Mayerl, et.al., Impact of Oatp1c1 deficiency on thyroid hormone metabolism and action in the mouse brain., Endocrinology, 2012, 153
  http://rdf.ncbi.nlm.nih.gov/pubmed/22294745