increased circulating thyroid-stimulating hormone level_Nkx2-1<tm1Shk>/Nkx2-1<+>

http://metadb.riken.jp/0005122I129S4SvJaeNkx21tm1ShkNkx21Nkx21tm1ShkNkx21

increased circulating thyroid-stimulating hormone level_Nkx2-1<tm1Shk>/Nkx2-1<+>

表現型アノテーション

MGI marker

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

• NK2 homeobox 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:108067

遺伝子型

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

• Nkx2-1<tm1Shk>/Nkx2-1<+>

アレルシンボル

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

• Nkx2-1<tm1Shk>|Nkx2-1<+>

遺伝的背景

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

• involves: 129S4/SvJae

MP annotation

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

• increased circulating thyroid-stimulating hormone level
  http://purl.obolibrary.org/obo/MP_0005122

文献

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

• Joachim. Pohlenz, et.al., Partial deficiency of thyroid transcription factor 1 produces predominantly neurological defects in humans and mice., The Journal of clinical investigation, 2002, 109
  http://rdf.ncbi.nlm.nih.gov/pubmed/11854318