no abnormal phenotype detected_Slc44a2<tm1.1Tec>/Slc44a2<tm1.1Tec>

http://metadb.riken.jp/0002169I129S1Sv129X1SvJC57BL6SJLJSlc44a2tm11TecSlc44a2tm11TecSlc44a2tm11Tec

no abnormal phenotype detected_Slc44a2<tm1.1Tec>/Slc44a2<tm1.1Tec>

表現型アノテーション

MGI marker

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

• solute carrier family 44, member 2
  http://metadb.riken.jp/db/mgi_rdf/MGI:1915932

遺伝子型

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

• Slc44a2<tm1.1Tec>/Slc44a2<tm1.1Tec>

アレルシンボル

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

• Slc44a2<tm1.1Tec>

遺伝的背景

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

• involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL/J

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

• Pavan. Kommareddi, et.al., Hair Cell Loss, Spiral Ganglion Degeneration, and Progressive Sensorineural Hearing Loss in Mice with Targeted Deletion of Slc44a2/Ctl2., Journal of the Association for Research in Otolaryngology : JARO, 2015, 16
  http://rdf.ncbi.nlm.nih.gov/pubmed/26463873