no abnormal phenotype detected_Ret<tm3(RET)Jmi>/Ret<+>

http://metadb.riken.jp/0002169NSRettm3RETJmiRetRetRettm3RETJmi

no abnormal phenotype detected_Ret<tm3(RET)Jmi>/Ret<+>

表現型アノテーション

MGI marker

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

• ret proto-oncogene
  http://metadb.riken.jp/db/mgi_rdf/MGI:97902

遺伝子型

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

• Ret<tm3(RET)Jmi>/Ret<+>

アレルシンボル

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

• Ret<+>|Ret<tm3(RET)Jmi>

遺伝的背景

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

• Not Specified

MP annotation

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

• no abnormal phenotype detected
  http://purl.obolibrary.org/obo/MP_0002169

文献

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

• Sanjay. Jain, et.al., Mice expressing a dominant-negative Ret mutation phenocopy human Hirschsprung disease and delineate a direct role of Ret in spermatogenesis., Development (Cambridge, England), 2004, 131
  http://rdf.ncbi.nlm.nih.gov/pubmed/15469971