impaired hearing_Col11a2<tm1Mne>/Col11a2<tm1Mne>

http://metadb.riken.jp/0006325FVB129Col11a2tm1MneCol11a2tm1MneCol11a2tm1MneCol11a2tm1Mne

impaired hearing_Col11a2<tm1Mne>/Col11a2<tm1Mne>

表現型アノテーション

MGI marker

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

• collagen, type XI, alpha 2
  http://metadb.riken.jp/db/mgi_rdf/MGI:88447

遺伝子型

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

• Col11a2<tm1Mne>/Col11a2<tm1Mne>

アレルシンボル

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

• Col11a2<tm1Mne>

遺伝的背景

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

• FVB.129-Col11a2<tm1Mne>

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

• S W. Li, et.al., Targeted disruption of Col11a2 produces a mild cartilage phenotype in transgenic mice: comparison with the human disorder otospondylomegaepiphyseal dysplasia (OSMED)., Developmental dynamics : an official publication of the American Association of Anatomists, 2001, 222
  http://rdf.ncbi.nlm.nih.gov/pubmed/11668593
• W T. McGuirt, et.al., Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13)., Nature genetics, 1999, 23
  http://rdf.ncbi.nlm.nih.gov/pubmed/10581026