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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
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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)
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Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory