abnormal retinal pigmentation_Lmo7<tm1Tilg>/Lmo7<tm1Tilg>

http://metadb.riken.jp/0005103I129S7SvEvBrdC57BL6Lmo7tm1TilgLmo7tm1TilgLmo7tm1Tilg

abnormal retinal pigmentation_Lmo7<tm1Tilg>/Lmo7<tm1Tilg>

表現型アノテーション

MGI marker

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

• LIM domain only 7
  http://metadb.riken.jp/db/mgi_rdf/MGI:1353586

遺伝子型

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

• Lmo7<tm1Tilg>/Lmo7<tm1Tilg>

アレルシンボル

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

• Lmo7<tm1Tilg>

遺伝的背景

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

• involves: 129S7/SvEvBrd * C57BL/6

MP annotation

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

• abnormal retinal pigmentation
  http://purl.obolibrary.org/obo/MP_0005103

文献

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

• Ekaterina. Semenova, et.al., An engineered 800 kilobase deletion of Uchl3 and Lmo7 on mouse chromosome 14 causes defects in viability, postnatal growth and degeneration of muscle and retina., Human molecular genetics, 2003, 12
  http://rdf.ncbi.nlm.nih.gov/pubmed/12761045