alopecia_Ctsl<tm1Cptr>/Ctsl<tm1Cptr>

http://metadb.riken.jp/0000414I129P2OlaHsdC57BL6JCtsltm1CptrCtsltm1CptrCtsltm1Cptr

alopecia_Ctsl<tm1Cptr>/Ctsl<tm1Cptr>

表現型アノテーション

MGI marker

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

• cathepsin L
  http://metadb.riken.jp/db/mgi_rdf/MGI:88564

遺伝子型

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

• Ctsl<tm1Cptr>/Ctsl<tm1Cptr>

アレルシンボル

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

• Ctsl<tm1Cptr>

遺伝的背景

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

• involves: 129P2/OlaHsd * C57BL/6J

MP annotation

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

• alopecia
  http://purl.obolibrary.org/obo/MP_0000414

文献

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

• W. Roth, et.al., Cathepsin L deficiency as molecular defect of furless: hyperproliferation of keratinocytes and pertubation of hair follicle cycling., FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2000, 14
  http://rdf.ncbi.nlm.nih.gov/pubmed/11023992