Symbol Name ID |
Smoc1
SPARC related modular calcium binding 1 MGI:1929878 |
Darker colors indicate more annotations |
Human Phenotypes | Optic atrophy |
Anophthalmia |
True anophthalmia |
Microphthalmia |
Disease(s) Associated with SMOC1 | ||||
microphthalmia with limb anomalies |
Mouse Phenotypes | impaired pupillary reflex |
abnormal retina vasculature morphology |
abnormal retina blood vessel morphology |
decreased retina ganglion cell number |
abnormal optic disk morphology |
absent optic nerve |
optic nerve hypoplasia |
abnormal retina pigment epithelium morphology |
mydriasis |
iris coloboma |
abnormal lens morphology |
retina coloboma |
microphthalmia |
narrow eye opening |
abnormal retina morphology |
retina degeneration |
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Availability | Mouse Genotype | ||||||||||||||||
Smoc1tm1a(EUCOMM)Wtsi/Smoc1tm1a(EUCOMM)Wtsi | |||||||||||||||||
Smoc1tm1b(EUCOMM)Wtsi/Smoc1tm1b(EUCOMM)Wtsi | |||||||||||||||||
Smoc1Tn(sb-lacZ,GFP)IR3.PV384Jtak/Smoc1Tn(sb-lacZ,GFP)IR3.PV384Jtak | |||||||||||||||||
Smoc1tm1b(EUCOMM)Wtsi/Smoc1+ |
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 08/21/2024 MGI 6.24 |
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