Snai2 Phenotype Annotations - Multigenic Genotypes

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Snai2
snail family zinc finger 2
MGI:1096393

31 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Kit^W-v/Kit⁺ Snai2^tm2Grid/Snai2⁺ involves: 129S1/Sv * C57BL	variable body spotting	J:80529
Kit^W-v/Kit⁺ Snai2^tm2Grid/Snai2^tm2Grid involves: 129S1/Sv * C57BL	variable body spotting	J:80529
Meox2^tm1(cre)Sor/Meox2⁺ Snai1^tm1Grid/Snai1^tm2Grid Snai2^tm2Grid/Snai2^tm2Grid involves: 129S1/Sv * 129S4/SvJaeSor * C57BL/6	embryonic growth retardation	J:111702
	normal nervous system phenotype	J:111702
	open neural tube	J:111702
Snai1^tm1Grid/Snai1⁺ Snai2^tm2Grid/Snai2^tm2Grid involves: 129S1/Sv * C57BL/6	cleft palate	J:121243
	neonatal lethality, complete penetrance	J:121243
	persistence of medial edge epithelium during palatal shelf fusion	J:121243
Snai1^tm1Grid/Snai1^tm2Grid Snai2^tm2Grid/Snai2^tm2Grid H2az2^{Tg(Wnt1-cre)11Rth}/H2az2⁺ involves: 129S1/Sv * C57BL/6 * CBA	abnormal Meckel's cartilage morphology	J:121243
	abnormal palatal shelf morphology	J:121243
	cleft palate	J:121243
	domed cranium	J:121243
	failure of palatal shelf elevation	J:121243
	frontal bone foramen	J:121243
	neonatal lethality, complete penetrance	J:121243
	short mandible	J:121243
	short parietal bone	J:121243
Snai2^tm2Grid/Snai2⁺ Snai3^tm1.2Jhws/Snai3^tm1.2Jhws involves: 129/Sv * 129S1/Sv * C57BL/6	abnormal thymus cortex morphology	J:204710
	abnormal thymus medulla morphology	J:204710
	decreased B cell number	J:204710
	disorganized spleen B cell follicle	J:204710
Snai2^tm2Grid/Snai2^tm2Grid Snai3^tm1.2Jhws/Snai3⁺ involves: 129/Sv * 129S1/Sv * C57BL/6	abnormal thymus cortex morphology	J:204710
	abnormal thymus medulla morphology	J:204710
	decreased B cell number	J:204710
	disorganized spleen B cell follicle	J:204710
	increased macrophage cell number	J:204710
	increased neutrophil cell number	J:204710
Snai2^tm2Grid/Snai2^tm2Grid Snai3^tm1.2Jhws/Snai3^tm1.2Jhws involves: 129/Sv * 129S1/Sv * C57BL/6	abnormal eye morphology	J:204710
	abnormal thymus cortex morphology	J:204710
	abnormal thymus involution	J:204710
	abnormal thymus medulla morphology	J:204710
	decreased B cell number	J:204710
	decreased body weight	J:204710
	decreased double-positive T cell number	J:204710
	disorganized spleen B cell follicle	J:204710
	increased macrophage cell number	J:204710
	increased neutrophil cell number	J:204710
	increased single-positive T cell number	J:204710
	lethality, incomplete penetrance	J:204710
	male infertility	J:204710
	premature death	J:204710
	small spleen	J:204710
	small thymus	J:204710
	thymus fibrosis	J:204710

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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