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Human Disease and Mouse Model Detail
Human Disease

Term: Klippel-Feil Syndrome 2, Autosomal Recessive; KFS2
OMIM ID: 214300

Synonyms Cervical Vertebral Fusion, Autosomal Recessive; Kfs, Autosomal Recessive
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...
     
Meox1 MEOX1
  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