Symbol Name ID |
Six3
sine oculis-related homeobox 3 MGI:102764 |
! | Indicates phenotype varies with strain background. |
Darker colors indicate more annotations |
Human Phenotypes | Dandy-Walker malformation |
Microcephaly |
Encephalocele |
Anosmia |
Hyposmia |
Anterior pituitary agenesis |
Anterior hypopituitarism |
Panhypopituitarism |
Spasticity |
Abnormal nervous system morphology |
Hydrocephalus |
Aplasia/Hypoplasia of the corpus callosum |
Agenesis of corpus callosum |
Aplasia/Hypoplasia of the cerebellum |
Cerebellar hypoplasia |
Holoprosencephaly |
Alobar holoprosencephaly |
Semilobar holoprosencephaly |
Spinal dysraphism |
Spinal cord tumor |
Abnormality of neuronal migration |
Chorea |
Cognitive impairment |
Intellectual disability |
Dystonia |
Global developmental delay |
Seizure |
Disease(s) Associated with SIX3 | |||||||||||||||||||||||||||
holoprosencephaly | |||||||||||||||||||||||||||
holoprosencephaly 2 |
Mouse Phenotypes | abnormal neural tube morphology |
abnormal forebrain development |
absent embryonic telencephalon |
holoprosencephaly |
decreased forebrain size |
increased midbrain size |
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Availability | Mouse Genotype | ||||||
Six3tm1Gco/Six3tm1Gco | |||||||
Six3tm2.1Gco/Six3tm2.1Gco | |||||||
Six3tm4(cre/ERT2)Gco/Six3+ | ! | ||||||
Six3tm3Gco/Six3tm3Gco Foxg1tm1(cre)Skm/Foxg1+ (conditional) |
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Six3tm2Gco/Six3tm2.1Gco Tg(Pax6-cre,GFP)1Pgr/0 (conditional) |
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 04/30/2024 MGI 6.23 |
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