About Help FAQ

Symbol
Name
ID

Snx10
sorting nexin 10
MGI:1919232

Phenotype annotations related to craniofacial

Darker colors indicate more annotations

Human Phenotypes	Frontal bossing	Macrocephaly	Facial palsy
Disease(s) Associated with SNX10
autosomal recessive osteopetrosis 8

Mouse Phenotypes		failure of tooth eruption	tooth impaction	absent teeth
Availability	Mouse Genotype	failure of tooth eruption	tooth impaction	absent teeth
	Snx10^em1Ael/Snx10^em1Ael
	Snx10^em2Ael/Snx10^em2Ael
	Snx10^{tm1a(EUCOMM)Raba}/Snx10^{tm1a(EUCOMM)Raba}
	Ctsk^tm1(cre)Ska/Ctsk⁺ Snx10^{tm1c(EUCOMM)Raba}/Snx10^{tm1c(EUCOMM)Raba} (conditional)

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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 04/23/2024 MGI 6.23