muscular atrophy_Hexb<tm1Rlp>/Hexb<tm1Rlp>

http://metadb.riken.jp/0002269I129S4SvJaeC57BL6Hexbtm1RlpHexbtm1RlpHexbtm1Rlp

muscular atrophy_Hexb<tm1Rlp>/Hexb<tm1Rlp>

表現型アノテーション

MGI marker

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

• hexosaminidase B
  http://metadb.riken.jp/db/mgi_rdf/MGI:96074

遺伝子型

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

• Hexb<tm1Rlp>/Hexb<tm1Rlp>

アレルシンボル

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

• Hexb<tm1Rlp>

遺伝的背景

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

• involves: 129S4/SvJae * C57BL/6

MP annotation

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

• muscular atrophy
  http://purl.obolibrary.org/obo/MP_0002269

文献

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

• K. Sango, et.al., Mouse models of Tay-Sachs and Sandhoff diseases differ in neurologic phenotype and ganglioside metabolism., Nature genetics, 1995, 11
  http://rdf.ncbi.nlm.nih.gov/pubmed/7550345