Snx3 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Snx3
sorting nexin 3
MGI:1860188

21 phenotypes from 1 allele in 1 genetic background

Allelic Composition Genetic Background	Annotated Term	Reference
Snx3^{tm1.1(KOMP)Vlcg}/Snx3⁺ C57BL/6N-Snx3^{tm1.1(KOMP)Vlcg}/J	increased blood urea nitrogen level	J:211773
	increased mean corpuscular volume	J:211773
Snx3^{tm1.1(KOMP)Vlcg}/Snx3^{tm1.1(KOMP)Vlcg} C57BL/6N-Snx3^{tm1.1(KOMP)Vlcg}/J	abnormal craniofacial morphology	J:211773
	abnormal embryo size	J:211773
	abnormal facial morphology	J:211773
	abnormal forebrain morphology	J:211773
	abnormal head shape	J:211773
	abnormal hindbrain morphology	J:211773
	abnormal limb morphology	J:211773
	abnormal midbrain morphology	J:211773
	abnormal neural tube closure	J:211773
	abnormal tail morphology	J:211773
	anophthalmia	J:211773
	cleft palate	J:211773
	edema	J:211773
	exencephaly	J:211773
	microphthalmia	J:211773
	pallor	J:211773
	preweaning lethality, complete penetrance	J:211773
	spina bifida	J:211773
	syndactyly	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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