muscle hypoplasia_Samd4<m1Btlr>/Samd4<m1Btlr>

http://metadb.riken.jp/0000734C57BL6JSamd4m1BtlrSamd4m1BtlrSamd4m1BtlrSamd4m1Btlr

muscle hypoplasia_Samd4<m1Btlr>/Samd4<m1Btlr>

表現型アノテーション

MGI marker

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

• sterile alpha motif domain containing 4
  http://metadb.riken.jp/db/mgi_rdf/MGI:1921730

遺伝子型

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

• Samd4<m1Btlr>/Samd4<m1Btlr>

アレルシンボル

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

• Samd4<m1Btlr>

遺伝的背景

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

• C57BL/6J-Samd4<m1Btlr>

MP annotation

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

• muscle hypoplasia
  http://purl.obolibrary.org/obo/MP_0000734

文献

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

• Zhe. Chen, et.al., Mutation of mouse Samd4 causes leanness, myopathy, uncoupled mitochondrial respiration, and dysregulated mTORC1 signaling., Proceedings of the National Academy of Sciences of the United States of America, 2014, 111
  http://rdf.ncbi.nlm.nih.gov/pubmed/24799716