cochlear ganglion degeneration_Phex<Hyp-Duk>/Y

http://metadb.riken.jp/0002857IBALBcAnBomUrdPhexHypDukYPhexHypDuk

cochlear ganglion degeneration_Phex<Hyp-Duk>/Y

表現型アノテーション

MGI marker

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

• phosphate regulating endopeptidase homolog, X-linked
  http://metadb.riken.jp/db/mgi_rdf/MGI:107489

遺伝子型

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

• Phex<Hyp-Duk>/Y

アレルシンボル

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

• Phex<Hyp-Duk>

遺伝的背景

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

• involves: BALB/cAnBomUrd

MP annotation

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

• cochlear ganglion degeneration
  http://purl.obolibrary.org/obo/MP_0002857

文献

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

• Bettina. Lorenz-Depiereux, et.al., New intragenic deletions in the Phex gene clarify X-linked hypophosphatemia-related abnormalities in mice., Mammalian genome : official journal of the International Mammalian Genome Society, 2004, 15
  http://rdf.ncbi.nlm.nih.gov/pubmed/15029877
• Cliff A. Megerian, et.al., A mouse model with postnatal endolymphatic hydrops and hearing loss., Hearing research, 2008, 237
  http://rdf.ncbi.nlm.nih.gov/pubmed/18289812