About   Help   FAQ
Human Disease and Mouse Model Detail
Human Disease

Term: Methylmalonic Aciduria and Homocystinuria, CblF Type
OMIM ID: 277380

Synonyms Cobalamin, Defect in Lysosomal Release of; Cobalamin F Disease; CBLF; Methylmalonic Acidemia and Homocystinuria, Cblf Type; Methylmalonic Aciduria Due to Vitamin B12-Release Defect; Vitamin B12 Lysosomal Release Defect; Vitamin B12 Storage Disease
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...
     
Lmbrd1 LMBRD1
  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
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support. 		last database update
04/03/2013
MGI 5.12 		The Jackson Laboratory