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Genes Phenotypes

Gene: Supt3

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Name
SPT3, SAGA and STAGA complex component
MGI ID
MGI:1923723
Synonyms
2310066G22Rik SPT3 SPT3L Supt3h
Viability
Homozygous - Lethal
Embryo viewer
N/A
Other links
MGI   Ensembl  
Significant phenotypes (2) Measurements chart (350) All data table (961)
Expression & images (0) Disease models (0) Order (1)
Significant
Not Significant
Not tested
View body weight measurements
Phenotype System Allele Zyg Sex Life Stage P Value
preweaning lethality, complete penetrance Supt3tm1a(EUCOMM)Hmgu HOM   Early adult 0.00
decreased circulating calcium level Supt3tm1a(EUCOMM)Hmgu HET Early adult 1.90×10-07

Download data as:  TSV  XLS

Select physiological systems to view:
Viewing: all phenotypes
Select physiological systems to view:
Viewing: all phenotypes

 Expression

Expression data not available

 Associated Images

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X-ray: XRay Images Whole Body Dorso Ventral
14 Images
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X-ray: XRay Images Skull Dorso Ventral Orientation
14 Images
X-ray: XRay Images Skull Lateral Orientation
14 Images
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DSS Histology
7 Images
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X-ray: XRay Images Whole Body Lateral Orientation
14 Images
X-ray: XRay Images Forepaw
13 Images
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Anti-nuclear antibody assay
6 Images
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Eye Morphology: Images Slit Lamp
1 Images
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Eye Morphology: Images Ophthalmoscopy
1 Images
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Ear epidermis immunophenotyping
12 Images
Legacy Phenotype Associated Images
Supt3tm1a(EUCOMM)Hmgu
WT, Male, WTSI
Supt3tm1a(EUCOMM)Hmgu
WT, Male, WTSI
Supt3tm1a(EUCOMM)Hmgu
WT, Male, WTSI
Supt3tm1a(EUCOMM)Hmgu
WT, Male, WTSI
Supt3tm1a(EUCOMM)Hmgu
WT, Male, WTSI

View all 120 images

Supt3tm1a(EUCOMM)Hmgu
abnormal retinal pigmentation, HET, Male, WTSI
Supt3tm1a(EUCOMM)Hmgu
fused cornea and lens, HET, Female, WTSI
Supt3tm1a(EUCOMM)Hmgu
abnormal coat/hair pigmentation, WT, Male, WTSI

 Disease Models

No associations by disease annotation and gene orthology found.
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 Order Mouse and ES Cells

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MGI Allele Allele Type Produced
Supt3tm1a(EUCOMM)Hmgu KO first allele (reporter-tagged insertion with conditional potential) Mice, Targeting vectors, ES Cells

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