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Human Disease and Mouse Model Detail
Human Disease

Term: Vitamin D Hydroxylation-Deficient Rickets, Type 1B; VDDR1B
OMIM ID: 600081

Synonyms 25-hydroxyvitamin D3 Deficiency, Selective; Pseudovitamin D3 Deficiency Rickets Due to 25-Hydroxylase Deficiency; Vitamin D-Dependent Rickets, Type 1b
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...
     
Cyp2r1 CYP2R1
  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