About   Help   FAQ
Symbol
Name
ID
Smoc1
SPARC related modular calcium binding 1
MGI:1929878
Phenotype annotations related to craniofacial
Darker colors indicate more annotations
Human Phenotypes
Frontal bossing
Micrognathia
Retrognathia
Hypoplasia of the premaxilla
Hypoplasia of the maxilla
Prominent forehead
Deep philtrum
Long philtrum
Cleft upper lip
Thin vermilion border
Cleft palate
High palate
Macrodontia
Flared nostrils
Depressed nasal bridge
Short nose
Abnormal eyebrow morphology
Abnormal eyelash morphology
Blepharophimosis
Short palpebral fissure
Downslanted palpebral fissures
Disease(s) Associated with SMOC1
microphthalmia with limb anomalies

Mouse Phenotypes
abnormal cranium morphology
abnormal maxilla morphology
cleft palate
high palate
abnormal snout morphology
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+

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
04/30/2024
MGI 6.23
The Jackson Laboratory