About   Help   FAQ
Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Smoc1
SPARC related modular calcium binding 1
MGI:1929878
55 phenotypes from 3 alleles in 5 genetic backgrounds
Export: Excel File
Allelic Composition
Genetic Background		 Annotated Term Reference
Smoc1tm1a(EUCOMM)Wtsi/Smoc1+
C57BL/6N-Smoc1tm1a(EUCOMM)Wtsi/H 		abnormal coat/hair pigmentation J:165965
decreased body weight J:165965
Smoc1tm1a(EUCOMM)Wtsi/Smoc1tm1a(EUCOMM)Wtsi
C57BL/6N-Smoc1tm1a(EUCOMM)Wtsi 		abnormal retina pigment epithelium morphology J:174198
absent fibula J:174198
cleft palate J:174198
decreased body size J:174198
decreased embryo size J:174198
iris coloboma J:174198
neonatal lethality, complete penetrance J:174198
optic nerve hypoplasia J:174198
retina coloboma J:174198
syndactyly J:174198
Smoc1tm1b(EUCOMM)Wtsi/Smoc1+
C57BL/6N-Smoc1tm1b(EUCOMM)Wtsi/H 		abnormal lens morphology J:211773
abnormal maxilla morphology J:211773
decreased circulating iron level J:211773
decreased erythrocyte cell number J:211773
decreased lymphocyte cell number J:211773
increased basophil cell number J:211773
increased heart weight J:211773
increased large unstained cell number J:211773
increased neutrophil cell number J:211773
increased red blood cell distribution width J:211773
Smoc1tm1b(EUCOMM)Wtsi/Smoc1tm1b(EUCOMM)Wtsi
C57BL/6N-Smoc1tm1b(EUCOMM)Wtsi/H 		abnormal cranium morphology J:211773
abnormal digit morphology J:211773
abnormal gait J:211773
abnormal head size J:211773
abnormal maxilla morphology J:211773
abnormal optic disk morphology J:211773
abnormal pelvic girdle bone morphology J:211773
abnormal retina blood vessel morphology J:211773
abnormal retina morphology J:211773
abnormal retina vasculature morphology J:211773
abnormal snout morphology J:211773
decreased lymphocyte cell number J:211773
impaired pupillary reflex J:211773
increased neutrophil cell number J:211773
mydriasis J:211773
narrow eye opening J:211773
preweaning lethality, incomplete penetrance J:211773
short tibia J:211773
syndactyly J:211773
Smoc1Tn(sb-lacZ,GFP)IR3.PV384Jtak/Smoc1Tn(sb-lacZ,GFP)IR3.PV384Jtak
involves: C3H * C57BL/6J * DBA/2 		abnormal hindlimb morphology J:169180
abnormal interdigital cell death J:169180
abnormal joint morphology J:169180
abnormal pollex morphology J:169180
abnormal retina morphology J:169180
abnormal retina pigment epithelium morphology J:169180
absent optic nerve J:169180
bowed tibia J:169180
clubfoot J:169180
decreased body size J:169180
decreased body weight J:169180
decreased retina ganglion cell number J:169180
fused metatarsal bones J:169180
high palate J:169180
interdigital webbing J:169180
microphthalmia J:169180
optic nerve hypoplasia J:169180
pes valgus J:169180
postnatal growth retardation J:169180
postnatal lethality, complete penetrance J:169180
retina degeneration J:169180
short fibula J:169180
syndactyly J:169180
synostosis J:169180
Smoc1Tn(sb-lacZ,GFP)IR3.PV384Jtak/Smoc1Tn(sb-lacZ,GFP)IR3.PV384Jtak
involves: C3H * C57BL/6J * DBA/2 * ICR 		cleft palate J:169180
clubfoot J:169180
syndactyly J:169180
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
11/05/2024
MGI 6.24 		The Jackson Laboratory