polychromatophilia_Samd9l<tm1Homy>/Samd9l<tm1Homy>

http://metadb.riken.jp/0005097I129P2OlaHsdSamd9ltm1HomySamd9ltm1HomySamd9ltm1Homy

polychromatophilia_Samd9l<tm1Homy>/Samd9l<tm1Homy>

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 9-like
  http://metadb.riken.jp/db/mgi_rdf/MGI:1343184

遺伝子型

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

• Samd9l<tm1Homy>/Samd9l<tm1Homy>

アレルシンボル

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

• Samd9l<tm1Homy>

遺伝的背景

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

• involves: 129P2/OlaHsd

MP annotation

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

• polychromatophilia
  http://purl.obolibrary.org/obo/MP_0005097

文献

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

• Akiko. Nagamachi, et.al., Haploinsufficiency of SAMD9L, an endosome fusion facilitator, causes myeloid malignancies in mice mimicking human diseases with monosomy 7., Cancer cell, 2013, 24
  http://rdf.ncbi.nlm.nih.gov/pubmed/24029230