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Human Disease and Mouse Model Detail
Human Disease

Term: 17-beta Hydroxysteroid Dehydrogenase III Deficiency
OMIM ID: 264300

Synonyms 17-ketosteroid Reductase Deficiency of Testis; 17-ksr Deficiency; Neutral 17-Beta-Hydroxysteroid Oxidoreductase Deficiency
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...
     
Hsd17b3 HSD17B3
  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