abnormal myelination_Hpn<tm1Qwu>/Hpn<tm1Qwu>

http://metadb.riken.jp/0000920I129X1SvJNIHSwissHpntm1QwuHpntm1QwuHpntm1Qwu

abnormal myelination_Hpn<tm1Qwu>/Hpn<tm1Qwu>

表現型アノテーション

MGI marker

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

• hepsin
  http://metadb.riken.jp/db/mgi_rdf/MGI:1196620

遺伝子型

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

• Hpn<tm1Qwu>/Hpn<tm1Qwu>

アレルシンボル

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

• Hpn<tm1Qwu>

遺伝的背景

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

• involves: 129X1/SvJ * NIH Swiss

MP annotation

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

• abnormal myelination
  http://purl.obolibrary.org/obo/MP_0000920

文献

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

• Michel. Guipponi, et.al., Mice deficient for the type II transmembrane serine protease, TMPRSS1/hepsin, exhibit profound hearing loss., The American journal of pathology, 2007, 171
  http://rdf.ncbi.nlm.nih.gov/pubmed/17620368