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All Matches for Hesx1tm1Icar
You searched for: hesx1. Also searched for: hesx1-.
Symbol
Name
ID
Hesx1tm1Icar
homeobox gene expressed in ES cells; targeted mutation 1, Iain C A F Robinson
MGI:90332

Nomenclature or ID Symbol, Name, Synonym and Accession ID matches to your query for this genome feature.
  Score Nomenclature or ID
Marker Symbol : Hesx1
Allele Synonym : Hesx1-
Allele Symbol : Hesx1tm1Icar

Vocabulary Terms Term, Synonym, and Definition matches to your query that are associated with this genome feature.
  Score Annotated Term
Disease Model : septooptic dysplasia
    from its definition : A syndrome characterized by the classical triad of optic nerve hypoplasia, pituitary gland hypoplasia and midline brain defects that has_material_basis_in mutation in the HESX1 gene on chromosome 3p14.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
11/23/2021
MGI 6.17
The Jackson Laboratory