abnormal skin pigmentation_Del(7)Tyr<c-3H>/Del(7)Tyr<c-3H>

http://metadb.riken.jp/0002095I101HC3HHeHDel7Tyrc3HDel7Tyrc3HDel7Tyrc3H

abnormal skin pigmentation_Del(7)Tyr<c-3H>/Del(7)Tyr<c-3H>

表現型アノテーション

MGI marker

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

• deletion, Chr 7, albino 3 Harwell
  http://metadb.riken.jp/db/mgi_rdf/MGI:4431232

遺伝子型

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

• Del(7)Tyr<c-3H>/Del(7)Tyr<c-3H>

アレルシンボル

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

• Del(7)Tyr<c-3H>

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

• abnormal skin pigmentation
  http://purl.obolibrary.org/obo/MP_0002095

文献

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

• R P. Erickson, et.al., Glucose-6-phosphatase deficiency caused by radiation-induced alleles at the albino locus in the mouse., Proceedings of the National Academy of Sciences of the United States of America, 1968, 59
  http://rdf.ncbi.nlm.nih.gov/pubmed/4296364