Smoc1 Phenotype Annotations

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

Allelic Composition Genetic Background	Annotated Term	Reference
Smoc1^{tm1a(EUCOMM)Wtsi}/Smoc1⁺ C57BL/6N-Smoc1^{tm1a(EUCOMM)Wtsi}/H	abnormal coat/hair pigmentation	J:165965
	decreased body weight	J:165965
Smoc1^{tm1a(EUCOMM)Wtsi}/Smoc1^{tm1a(EUCOMM)Wtsi} C57BL/6N-Smoc1^{tm1a(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
Smoc1^{tm1b(EUCOMM)Wtsi}/Smoc1⁺ C57BL/6N-Smoc1^{tm1b(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
Smoc1^{tm1b(EUCOMM)Wtsi}/Smoc1^{tm1b(EUCOMM)Wtsi} C57BL/6N-Smoc1^{tm1b(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
Smoc1^{Tn(sb-lacZ,GFP)IR3.PV384Jtak}/Smoc1^{Tn(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
Smoc1^{Tn(sb-lacZ,GFP)IR3.PV384Jtak}/Smoc1^{Tn(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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