impaired hearing_Atp2b2<Elfin>/Atp2b2<+>

http://metadb.riken.jp/0006325IC3HHeJC57BL6JAtp2b2ElfinAtp2b2Atp2b2Atp2b2Elfin

impaired hearing_Atp2b2<Elfin>/Atp2b2<+>

表現型アノテーション

MGI marker

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

• ATPase, Ca++ transporting, plasma membrane 2
  http://metadb.riken.jp/db/mgi_rdf/MGI:105368

遺伝子型

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

• Atp2b2<Elfin>/Atp2b2<+>

アレルシンボル

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

• Atp2b2<+>|Atp2b2<Elfin>

遺伝的背景

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

• involves: C3H/HeJ * C57BL/6J

MP annotation

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

• impaired hearing
  http://purl.obolibrary.org/obo/MP_0006325

文献

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

• Lin. Xu, et.al., Identification of a novel point mutation of mouse Atp2b2 induced by N-ethyl-N-nitrosourea mutagenesis., Experimental animals, 2011, 60
  http://rdf.ncbi.nlm.nih.gov/pubmed/21325754