Symbol
Name
ID

Smoc1
SPARC related modular calcium binding 1
MGI:1929878

Phenotype annotations related to vision/eye

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

abnormal placement of pupils

mydriasis

iris coloboma

abnormal lens morphology

retina coloboma

microphthalmia

narrow eye opening

abnormal retina morphology

retina degeneration

Availability

Mouse Genotype

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}

Smoc1^{tm1b(EUCOMM)Wtsi}/Smoc1⁺

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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