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Human Disease and Mouse Model Detail
Human Disease

Term: Feingold Syndrome 2; FGLDS2
OMIM ID: 614326

Synonyms Brachydactyly with Short Stature and Microcephaly
Transgenes and
other mutation types
Mirc1   Characteristics of this human disease are associated with transgenes and other mutation types in mouse.

Mouse Models
Genotype Ref(s)
Allelic Composition Note Genetic Background
Models involving transgenes or other mutation types.1
Mirc1tm1.2Tyj/Mirc1+   involves: 129S4/SvJae * C57BL/6 J:188762

1Models involving transgenes or other mutation types may also appear in other sections of the table.
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