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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Scx
scleraxis scleraxis bHLH transcription factor
MGI:102934
13 phenotypes from 5 alleles in 3 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Scxtm1.1(KOMP)Vlcg/Scxtm1.1(KOMP)Vlcg
C57BL/6N-Scxtm1.1(KOMP)Vlcg/Ucd
edema J:211773
microphthalmia J:211773
preweaning lethality, complete penetrance J:211773
Scxtm1.1Stzr/Scxtm1.1Stzr
Not Specified
abnormal tail morphology J:122742
abnormal tail movements J:122742
abnormal tendon morphology J:122742
abnormal tendon stiffness J:122742
absent deltoid tuberosity J:122742
impaired righting response J:122742
Scxtm1.1Stzr/Scxtm1.1Stzr
Tg(Scx-GFP)1Stzr/0
Not Specified
abnormal tail morphology J:122742
abnormal tail movements J:122742
abnormal tendon morphology J:122742
Scxtm1Eno/Scxtm2Eno
chimera involves: 129S7/SvEvBrd * C57BL/6 * Swiss
abnormal sclerotome morphology J:55991
absent somites J:55991
dilated dorsal aorta J:55991
Scxtm1Stzr/Scxtm1Stzr
Not Specified
no abnormal phenotype detected J:122742

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
12/10/2024
MGI 6.24
The Jackson Laboratory