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Symbol
Name
ID

Snx10
sorting nexin 10
MGI:1919232

Phenotype annotations related to hematopoietic system

Darker colors indicate more annotations

Human Phenotypes	Anemia	Thrombocytopenia	Splenomegaly
Disease(s) Associated with SNX10
autosomal recessive osteopetrosis 8

Mouse Phenotypes		decreased osteoclast cell number	abnormal osteoclast morphology	abnormal osteoclast physiology
Availability	Mouse Genotype	decreased osteoclast cell number	abnormal osteoclast morphology	abnormal osteoclast physiology
	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)
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