Snx27 Phenotype Annotations

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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)
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