absent otoliths_Slc26a4<tm1Egr>/Slc26a4<tm1Egr>

http://metadb.riken.jp/0002978EI129S6SvEvTacorI129S6SvEvTacBlackSwissSlc26a4tm1EgrSlc26a4tm1EgrSlc26a4tm1Egr

absent otoliths_Slc26a4<tm1Egr>/Slc26a4<tm1Egr>

表現型アノテーション

MGI marker

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

• solute carrier family 26, member 4
  http://metadb.riken.jp/db/mgi_rdf/MGI:1346029

遺伝子型

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

• Slc26a4<tm1Egr>/Slc26a4<tm1Egr>

アレルシンボル

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

• Slc26a4<tm1Egr>

遺伝的背景

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

• either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * Black Swiss)

MP annotation

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

• absent otoliths
  http://purl.obolibrary.org/obo/MP_0002978

文献

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

• L A. Everett, et.al., Targeted disruption of mouse Pds provides insight about the inner-ear defects encountered in Pendred syndrome., Human molecular genetics, 2001, 10
  http://rdf.ncbi.nlm.nih.gov/pubmed/11152663