Snap29 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Snap29
synaptosomal-associated protein 29
MGI:1914724

25 phenotypes from 3 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Snap29^{tm1a(EUCOMM)Wtsi}/Snap29⁺ C57BL/6N-Snap29^{tm1a(EUCOMM)Wtsi}/Wtsi	increased body weight	J:175295
	increased bone mineral content	J:175295
	increased bone mineral density	J:175295
	increased lean body mass	J:175295
Snap29^{tm1b(EUCOMM)Wtsi}/Snap29^{tm1b(EUCOMM)Wtsi} involves: C57BL/6N * FVB/N	abnormal autophagy	J:236759
	abnormal endoplasmic reticulum physiology	J:236759
	abnormal epidermal lamellar body morphology	J:236759
	abnormal skin appearance	J:236759
	abnormal skin physiology	J:236759
	acanthosis	J:236759
	decreased birth body size	J:236759
	hyperkeratosis	J:236759
	increased endoplasmic reticulum stress	J:236759
	scaly skin	J:236759
	tight skin	J:236759
Snap29^{tm1c(EUCOMM)Wtsi}/Snap29^{tm1c(EUCOMM)Wtsi} Tg(KRT14-cre)1Cgn/0 involves: C57BL/6 * C57BL/6N * DBA/2	abnormal corneocyte morphology	J:236759
	abnormal epidermal lamellar body morphology	J:236759
	abnormal epidermal layer morphology	J:236759
	abnormal epidermis stratum granulosum morphology	J:236759
	abnormal keratinocyte differentiation	J:236759
	abnormal skin appearance	J:236759
	abnormal skin physiology	J:236759
	absent gastric milk in neonates	J:236759
	acanthosis	J:236759
	decreased birth body size	J:236759
	decreased hair follicle number	J:236759
	decreased keratohyalin granule number	J:236759
	hyperkeratosis	J:236759
	impaired skin barrier function	J:236759
	increased keratinocyte proliferation	J:236759
	neonatal lethality, complete penetrance	J:236759
	scaly skin	J:236759
	tight skin	J:236759

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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