Svep1 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Svep1
sushi, von Willebrand factor type A, EGF and pentraxin domain containing 1
MGI:1928849

27 phenotypes from 2 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Svep1^{tm1a(EUCOMM)Hmgu}/Svep1^{tm1a(EUCOMM)Hmgu} involves: C57BL/6N	abnormal lymphangiogenesis	J:244466
	abnormal lymphatic vessel morphology	J:244466
	lymphedema	J:244466
	nuchal edema	J:244466
Svep1^{tm1b(EUCOMM)Hmgu}/Svep1⁺ C57BL/6N-Svep1^{tm1b(EUCOMM)Hmgu}/J	abnormal eyelid morphology	J:211773
	abnormal iris pigmentation	J:211773
	abnormal iris transillumination	J:211773
	cornea deposits	J:211773
	decreased circulating glucose level	J:211773
	decreased circulating phosphate level	J:211773
	decreased circulating sodium level	J:211773
	exophthalmos	J:211773
	eyelids fail to open	J:211773
	impaired pupillary reflex	J:211773
	increased erythrocyte cell number	J:211773
	increased hematocrit	J:211773
	increased hemoglobin content	J:211773
	narrow eye opening	J:211773
	prolonged QRS complex duration	J:211773
Svep1^{tm1b(EUCOMM)Hmgu}/Svep1^{tm1b(EUCOMM)Hmgu} B6N(Cg)-Svep1^{tm1b(EUCOMM)Hmgu}/J	abnormal limb morphology	J:255307
	abnormal skin coloration	J:255307
	abnormal tail morphology	J:255307
	acanthosis	J:255307
	edema	J:255307
	preweaning lethality, complete penetrance	J:255307
	thick epidermis	J:255307
Svep1^{tm1b(EUCOMM)Hmgu}/Svep1^{tm1b(EUCOMM)Hmgu} C57BL/6N-Svep1^{tm1b(EUCOMM)Hmgu}/J	abnormal limb morphology	J:211773
	abnormal skin appearance	J:211773
	abnormal tail morphology	J:211773
	edema	J:211773
	preweaning lethality, complete penetrance	J:211773

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