About Help FAQ

Symbol
Name
ID

Smoc1
SPARC related modular calcium binding 1
MGI:1929878

Phenotype annotations related to nervous system

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	decreased retina ganglion cell number	abnormal optic disk morphology	absent optic nerve	optic nerve hypoplasia
	Smoc1^{tm1a(EUCOMM)Wtsi}/Smoc1^{tm1a(EUCOMM)Wtsi}
	Smoc1^{tm1b(EUCOMM)Wtsi}/Smoc1^{tm1b(EUCOMM)Wtsi}
	Smoc1^{Tn(sb-lacZ,GFP)IR3.PV384Jtak}/Smoc1^{Tn(sb-lacZ,GFP)IR3.PV384Jtak}

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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 05/14/2024 MGI 6.23