deafness_Clrn1<tm2.1Kuna>/Clrn1<tm2.1Kuna>

http://metadb.riken.jp/0001967I129BALBcJC57BL6JClrn1tm21KunaClrn1tm21KunaClrn1tm21Kuna

deafness_Clrn1<tm2.1Kuna>/Clrn1<tm2.1Kuna>

表現型アノテーション

MGI marker

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

• clarin 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:2388124

遺伝子型

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

• Clrn1<tm2.1Kuna>/Clrn1<tm2.1Kuna>

アレルシンボル

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

• Clrn1<tm2.1Kuna>

遺伝的背景

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

• involves: 129 * BALB/cJ * C57BL/6J

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

• Ruishuang. Geng, et.al., The mechanosensory structure of the hair cell requires clarin-1, a protein encoded by Usher syndrome III causative gene., The Journal of neuroscience : the official journal of the Society for Neuroscience, 2012, 32
  http://rdf.ncbi.nlm.nih.gov/pubmed/22787034