Symbol Name ID |
Smoc1
SPARC related modular calcium binding 1 MGI:1929878 |
Darker colors indicate more annotations |
Human Phenotypes | Hydrocephalus |
Arrhinencephaly |
Intellectual disability |
Intellectual disability, moderate |
Intellectual disability, severe |
Global developmental delay |
Disease(s) Associated with SMOC1 | ||||||
microphthalmia with limb anomalies |
Mouse Phenotypes | decreased retina ganglion cell number |
abnormal optic disk morphology |
absent optic nerve |
optic nerve hypoplasia |
|
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 |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
||
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support. |
last database update 07/05/2024 MGI 6.24 |
|
|