Snx27 Phenotype Annotations

About Help FAQ

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Snx27
sorting nexin family member 27
MGI:1923992

15 phenotypes from 2 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Snx27^{tm1b(KOMP)Wtsi}/Snx27⁺ C57BL/6N-Snx27^{tm1b(KOMP)Wtsi}/Ucd	decreased erythrocyte cell number	J:211773
	decreased hematocrit	J:211773
	decreased hemoglobin content	J:211773
Snx27^{tm1b(KOMP)Wtsi}/Snx27^{tm1b(KOMP)Wtsi} C57BL/6N-Snx27^{tm1b(KOMP)Wtsi}/MbpMmucd	abnormal craniofacial morphology	J:211773
	edema	J:211773
Snx27^{tm1b(KOMP)Wtsi}/Snx27^{tm1b(KOMP)Wtsi} C57BL/6N-Snx27^{tm1b(KOMP)Wtsi}/Ucd	preweaning lethality, incomplete penetrance	J:211773
Snx27^tm1Lslo/Snx27^tm1Lslo involves: 129P2/OlaHsd	abnormal cell physiology	J:171001
	abnormal intestine morphology	J:171001
	postnatal growth retardation	J:171001
	postnatal lethality, complete penetrance	J:171001
	prenatal lethality, incomplete penetrance	J:171001
	slow postnatal weight gain	J:171001
	small heart	J:171001
	small liver	J:171001
	small spleen	J:171001

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 12/10/2024 MGI 6.24