deafness_Ush1c<dfcr>/Ush1c<dfcr>

http://metadb.riken.jp/0001967IBALBcBySmnC57BL6CB17Ush1cdfcrUsh1cdfcrUsh1cdfcr

deafness_Ush1c<dfcr>/Ush1c<dfcr>

表現型アノテーション

MGI marker

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

• USH1 protein network component harmonin
  http://metadb.riken.jp/db/mgi_rdf/MGI:1919338

遺伝子型

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

• Ush1c<dfcr>/Ush1c<dfcr>

アレルシンボル

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

• Ush1c<dfcr>

遺伝的背景

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

• involves: BALB/cBySmn * C57BL/6 * CB17

MP annotation

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

• deafness
  http://purl.obolibrary.org/obo/MP_0001967

文献

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

• Nicolas. Grillet, et.al., Harmonin mutations cause mechanotransduction defects in cochlear hair cells., Neuron, 2009, 62
  http://rdf.ncbi.nlm.nih.gov/pubmed/19447093