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Human Disease and Mouse Model Detail
Human Disease

Term: Mismatch Repair Cancer Syndrome; MMRCS
OMIM ID: 276300

Synonyms Brain Tumor-Polyposis Syndrome 1; BTPS1; Btp1 Syndrome; Childhood Cancer Syndrome; Constitutional Mismatch Repair Deficiency Syndrome; CMMRDS; Mismatch Repair Deficiency; Mmr Deficiency; Turcot Syndrome
Associated Genes

Orthologous mouse and human markers where mutations in one or both species have been associated with phenotypes characteristic of this disease.

Mouse Gene
Human Gene
 
Characteristics of this human disease are associated with mutations in...
     
Mlh1 MLH1
Msh2 MSH2
Msh6 MSH6
Pms2 PMS2
  human...the human gene.
     MGI data currently do not associate this disease with mutations in the orthologous mouse gene.
     
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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Send questions and comments to User Support. 		last database update
04/03/2013
MGI 5.12 		The Jackson Laboratory