paternal imprinting_T(7;18)50H/+

http://metadb.riken.jp/0003123I101HC3HHeHT71850HT71850H

paternal imprinting_T(7;18)50H/+

表現型アノテーション

MGI marker

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

• reciprocal translocation, Chr 7 and 18, Harwell 50
  http://metadb.riken.jp/db/mgi_rdf/MGI:103975
• reciprocal translocation, Chr 7 and 18, Harwell 50
  http://metadb.riken.jp/db/mgi_rdf/MGI:103976

遺伝子型

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

• T(7;18)50H/+

アレルシンボル

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

• +|T(7;18)50H
• T(7;18)50H|+

遺伝的背景

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

• involves: 101/H * C3H/HeH

MP annotation

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

• paternal imprinting
  http://purl.obolibrary.org/obo/MP_0003123

文献

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

• 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