microgliosis_Slc20a2<tm1a(EUCOMM)Wtsi>/Slc20a2<tm1a(EUCOMM)Wtsi>

http://metadb.riken.jp/0008918C57BL6NTacSlc20a2tm1aEUCOMMWtsiIegSlc20a2tm1aEUCOMMWtsiSlc20a2tm1aEUCOMMWtsiSlc20a2tm1aEUCOMMWtsi

microgliosis_Slc20a2<tm1a(EUCOMM)Wtsi>/Slc20a2<tm1a(EUCOMM)Wtsi>

表現型アノテーション

MGI marker

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

• solute carrier family 20, member 2
  http://metadb.riken.jp/db/mgi_rdf/MGI:97851

遺伝子型

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

• Slc20a2<tm1a(EUCOMM)Wtsi>/Slc20a2<tm1a(EUCOMM)Wtsi>

アレルシンボル

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

• Slc20a2<tm1a(EUCOMM)Wtsi>

遺伝的背景

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

• C57BL/6NTac-Slc20a2<tm1a(EUCOMM)Wtsi>/Ieg

MP annotation

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

• microgliosis
  http://purl.obolibrary.org/obo/MP_0008918

文献

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

• Nina. Jensen, et.al., Loss of function of Slc20a2 associated with familial idiopathic Basal Ganglia calcification in humans causes brain calcifications in mice., Journal of molecular neuroscience : MN, 2013, 51
  http://rdf.ncbi.nlm.nih.gov/pubmed/23934451