| Human Disease |
Smith-Lemli-Opitz Syndrome; SLOS OMIM ID: 270400 |
|||||||||||||||||||||
| Synonyms | Lethal Acrodysgenital Syndrome; Polydactyly, Sex Reversal, Renal Hypoplasia, and Unilobar Lung; RSH Syndrome; Rutledge Lethal Multiple Congenital Anomaly Syndrome; SLO Syndrome | |||||||||||||||||||||
| View all models | View ALL (4) mouse models for this human disease. | |||||||||||||||||||||
|
Genes and mouse models |
Mutations in human and/or mouse homologs are associated with this disease
|
|||||||||||||||||||||
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Dhcr7tm1Fdp/Dhcr7tm1Fdp |
involves: 129S4/SvJae | J:68084, J:165301 | View |
| Dhcr7tm2Fdp/Dhcr7tm2Fdp |
involves: 129S4/SvJae | J:106758 | View |
| Dhcr7tm1Fdp/Dhcr7tm2Fdp |
involves: 129S4/SvJae | J:106758 | View |
| Dhcr7tm1Gst/Dhcr7tm1Gst |
involves: 129P2/OlaHsd | J:71611 | View |
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 06/12/2013 MGI 5.14 |
|
|
|
||