Snx13 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Snx13
sorting nexin 13
MGI:2661416

15 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Snx13^tm1.1Frq/Snx13^tm1.1Frq involves: 129S1/Sv * 129X1/SvJ * C57BL/6	abnormal blood vessel morphology	J:117102
	abnormal capillary morphology	J:117102
	abnormal extraembryonic endoderm formation	J:117102
	abnormal extraembryonic tissue morphology	J:117102
	abnormal placenta labyrinth morphology	J:117102
	abnormal placenta morphology	J:117102
	abnormal placental labyrinth vasculature morphology	J:117102
	abnormal trophoblast giant cell morphology	J:117102
	decreased embryo size	J:117102
	embryonic lethality during organogenesis, complete penetrance	J:117102
	open neural tube	J:117102
	small placenta	J:117102
Snx13^{tm1b(EUCOMM)Hmgu}/Snx13⁺ C57BL/6N-Snx13^{tm1b(EUCOMM)Hmgu}/Ieg	decreased mean corpuscular volume	J:211773
	increased leukocyte cell number	J:211773
Snx13^{tm1b(EUCOMM)Hmgu}/Snx13^{tm1b(EUCOMM)Hmgu} C57BL/6N-Snx13^{tm1b(EUCOMM)Hmgu}/Ieg	preweaning lethality, complete penetrance	J:211773

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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