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Gene Expression Data
Assay Details
Assay
Reference: J:238567 Houtmeyers R, et al., Zic2 mutation causes holoprosencephaly via disruption of NODAL signalling. Hum Mol Genet. 2016 Sep 15;25(18):3946-3959
Assay type: RNA in situ
MGI Accession ID: MGI:5823402
Gene symbol: Otx2
Gene name: orthodenticle homeobox 2
Probe: pOtd9
Probe preparation: Double stranded labelled with digoxigenin RNA
Assay notes: Specimens were hybridized with probes for two different markers: Otx2 and T (assay MGI:5823401).
Results
Specimen 1A: embryonic day 9.5 (more )
Structure Level Pattern Image Note
TS15: future forebrain Present 1A
TS15: future midbrain Present 1A

Specimen 1B: embryonic day 9.5; Nodaltm2Rob/Nodal+ (more )
Structure Level Pattern Image Note
TS15: future forebrain Present 1B A hypomorphic mutation of Nodal (D600) has no phenotypic consequence in the heterozygote.
TS15: future midbrain Present 1B A hypomorphic mutation of Nodal (D600) has no phenotypic consequence in the heterozygote.

Specimen 1C: embryonic day 9.5; Nodaltm1Rob/Nodal+ (more )
Structure Level Pattern Image Note
TS15: future forebrain Present 1C Embryos heterozygous for a null allele of Nodal have no phenotype.
TS15: future midbrain Present 1C Embryos heterozygous for a null allele of Nodal have no phenotype.

Specimen 1D: embryonic day 9.5; Zic2Ku/Zic2+ (more )
Structure Level Pattern Image Note
TS15: future forebrain Present 1D Embryos heterozygous for the severe loss of function kumba (Ku) allele of Zic2 have no discernible phenotype.
TS15: future midbrain Present 1D Embryos heterozygous for the severe loss of function kumba (Ku) allele of Zic2 have no discernible phenotype.

Specimen 1E: embryonic day 9.5; Zic2Ku/Zic2Ku (more )
Structure Level Pattern Image Note
TS15: future forebrain Ambiguous 1E Embryos homozygous for the severe loss of function kumba (Ku) allele of Zic2 exhibit forebrain dysmorphology that can include a mild loss of telencephalic tissue.
TS15: future midbrain Present 1E Embryos homozygous for this allele never exhibit loss of diencephalon or mesencephalon.

Specimen 1F: embryonic day 9.5; Nodaltm2Rob/Nodaltm2Rob (more )
Structure Level Pattern Image Note
TS15: future forebrain Present 1F Embryos homozygous for the D600 allele of Nodal exhibit a spectrum of defects, including no phenotype.
TS15: future midbrain Present 1F Embryos homozygous for the D600 allele of Nodal exhibit a spectrum of defects, including no phenotype.

Specimen 1G: embryonic day 9.5; Nodaltm2Rob/Nodaltm2Rob (more )
Structure Level Pattern Image Note
TS15: future forebrain Absent 1G When homozygous, a hypomorphic mutations of Nodal (D600) can cause moderate truncation in which some of the midbrain is retained.
TS15: future midbrain Present 1G When homozygous, a hypomorphic mutations of Nodal (D600) can cause moderate truncation in which some of the midbrain is retained.

Specimen 1H: embryonic day 9.5; Nodaltm2Rob/Nodaltm2Rob (more )
Structure Level Pattern Image Note
TS15: future forebrain Absent 1H When homozygous, a hypomorphic mutations of Nodal (D600) can cause severe truncation I which all forebrain and midbrain tissue is absent.
TS15: future midbrain Absent 1H When homozygous, a hypomorphic mutations of Nodal (D600) can cause severe truncation I which all forebrain and midbrain tissue is absent.

Specimen 1I: embryonic day 9.5; Nodaltm1Rob/Nodal+, Zic2Ku/Zic2Ku (more )
Structure Level Pattern Image Note
TS15: future forebrain Ambiguous 1I Decreasing Nodal function on the Zic2 Ku background leads to moderate or severe truncation.
TS15: future midbrain Ambiguous 1I Decreasing Nodal function on the Zic2 Ku background leads to moderate or severe truncation.


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
03/25/2025
MGI 6.24
The Jackson Laboratory