thin skin_Slc9a1<tm1Smb>/Slc9a1<tm1Smb>

http://metadb.riken.jp/0001199I129X1SvJBlackSwissSlc9a1tm1SmbSlc9a1tm1SmbSlc9a1tm1Smb

thin skin_Slc9a1<tm1Smb>/Slc9a1<tm1Smb>

表現型アノテーション

MGI marker

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

• solute carrier family 9 (sodium/hydrogen exchanger), member 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:102462

遺伝子型

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

• Slc9a1<tm1Smb>/Slc9a1<tm1Smb>

アレルシンボル

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

• Slc9a1<tm1Smb>

遺伝的背景

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

• involves: 129X1/SvJ * Black Swiss

MP annotation

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

• thin skin
  http://purl.obolibrary.org/obo/MP_0001199

文献

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

• S M. Bell, et.al., Targeted disruption of the murine Nhe1 locus induces ataxia, growth retardation, and seizures., The American journal of physiology, 1999, 276
  http://rdf.ncbi.nlm.nih.gov/pubmed/10199808