B M. Cattanach, et.al., A candidate mouse model for Prader-Willi syndrome which shows an absence of Snrpn expression., Nature genetics, 1992, 2

http://rdf.ncbi.nlm.nih.gov/pubmed/1303278

B M. Cattanach, et.al., A candidate mouse model for Prader-Willi syndrome which shows an absence of Snrpn expression., Nature genetics, 1992, 2

pubmed

表現型アノテーション

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

• postnatal growth retardation_T(7;18)50H/+
  http://metadb.riken.jp/0001732I101HC3HHeHT71850HT71850H
• uniparental disomy_T(7;18)50H/+
  http://metadb.riken.jp/0008867I101HC3HHeHT71850HT71850H
• short humerus_T(7;18)50H/+
  http://metadb.riken.jp/0004351I101HC3HHeHT71850HT71850H
• embryonic lethality during organogenesis, incomplete penetrance_T(7;18)50H/+
  http://metadb.riken.jp/0011108I101HC3HHeHT71850HT71850H
• abnormal femur morphology_T(7;18)50H/+
  http://metadb.riken.jp/0000559I101HC3HHeHT71850HT71850H
• embryonic lethality, complete penetrance_T(7;18)50H/+
  http://metadb.riken.jp/0011092I101HC3HHeHT71850HT71850H
• increased growth rate_T(7;18)50H/+
  http://metadb.riken.jp/0002865I101HC3HHeHT71850HT71850H
• short femur_T(7;18)50H/+
  http://metadb.riken.jp/0003109I101HC3HHeHT71850HT71850H
• abnormal humerus morphology_T(7;18)50H/+
  http://metadb.riken.jp/0005296I101HC3HHeHT71850HT71850H
• abnormal pelvic girdle bone morphology_T(7;18)50H/+
  http://metadb.riken.jp/0004509I101HC3HHeHT71850HT71850H
• maternal imprinting_T(7;18)50H/+
  http://metadb.riken.jp/0003122I101HC3HHeHT71850HT71850H
• decreased diameter of humerus_T(7;18)50H/+
  http://metadb.riken.jp/0008154I101HC3HHeHT71850HT71850H
• short tail_T(7;18)50H/+
  http://metadb.riken.jp/0000592I101HC3HHeHT71850HT71850H
• decreased diameter of femur_T(7;18)50H/+
  http://metadb.riken.jp/0008152I101HC3HHeHT71850HT71850H
• postnatal lethality, incomplete penetrance_T(7;18)50H/+
  http://metadb.riken.jp/0011086I101HC3HHeHT71850HT71850H
• paternal imprinting_T(7;18)50H/+
  http://metadb.riken.jp/0003123I101HC3HHeHT71850HT71850H

トランスクリプトームデータ

http://rdf.ncbi.nlm.nih.gov/pubmed/

• CD09719
  http://metadb.riken.jp/db/BrainTx/TranscriptomeData/CD09719