Symbol Name ID |
Specc1l
sperm antigen with calponin homology and coiled-coil domains 1-like MGI:1921642 |
Darker colors indicate more annotations |
Human Phenotypes | Hypertelorism |
Proptosis |
Microphthalmia |
Coloboma |
Strabismus |
Ptosis |
Bilateral ptosis |
Disease(s) Associated with SPECC1L | |||||||
oblique facial clefting 1 | |||||||
Teebi hypertelorism syndrome 1 |
Mouse Phenotypes | coloboma |
|
Availability | Mouse Genotype | |
Specc1lem3Kumc/Specc1lem3Kumc | ||
Specc1lem4Kumc/Specc1lem4Kumc | ||
Specc1lem3Kumc/Specc1l+ | ||
Specc1lem4Kumc/Specc1l+ |
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 04/23/2024 MGI 6.23 |
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