hypotonia_Slc7a7<Gt(OST41878)Lex>/Slc7a7<Gt(OST41878)Lex>

http://metadb.riken.jp/0004144B6129SSlc7a7GtOST41878LexSlc7a7GtOST41878LexSlc7a7GtOST41878LexSlc7a7GtOST41878Lex

hypotonia_Slc7a7<Gt(OST41878)Lex>/Slc7a7<Gt(OST41878)Lex>

表現型アノテーション

MGI marker

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

• solute carrier family 7 (cationic amino acid transporter, y+ system), member 7
  http://metadb.riken.jp/db/mgi_rdf/MGI:1337120

遺伝子型

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

• Slc7a7<Gt(OST41878)Lex>/Slc7a7<Gt(OST41878)Lex>

アレルシンボル

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

• Slc7a7<Gt(OST41878)Lex>

遺伝的背景

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

• B6.129S-Slc7a7<Gt(OST41878)Lex>

MP annotation

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

• hypotonia
  http://purl.obolibrary.org/obo/MP_0004144

文献

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

• Maria Pia. Sperandeo, et.al., Slc7a7 disruption causes fetal growth retardation by downregulating Igf1 in the mouse model of lysinuric protein intolerance., American journal of physiology. Cell physiology, 2007, 293
  http://rdf.ncbi.nlm.nih.gov/pubmed/17376816