Slc26a2 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Slc26a2
solute carrier family 26 (sulfate transporter), member 2
MGI:892977

19 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Slc26a2^em1(IMPC)Bay/Slc26a2⁺ C57BL/6N-Slc26a2^em1(IMPC)Bay/BayMmucd	impaired glucose tolerance	J:211773
Slc26a2^em1(IMPC)Bay/Slc26a2^em1(IMPC)Bay C57BL/6N-Slc26a2^em1(IMPC)Bay/BayMmucd	abnormal facial morphology	J:211773
	abnormal limb morphology	J:211773
	abnormal tail morphology	J:211773
	preweaning lethality, complete penetrance	J:211773
	protruding tongue	J:211773
Slc26a2^tm1Aros/Slc26a2^tm1Aros involves: 129S7/SvEvBrd * C57BL/6J	abnormal cell physiology	J:97104
	abnormal joint morphology	J:97104
	abnormal long bone epiphysis morphology	J:97104
	abnormal long bone hypertrophic chondrocyte zone	J:97104
	bowed tibia	J:97104
	decreased cell proliferation	J:97104
	decreased length of long bones	J:97104
	delayed endochondral bone ossification	J:97104
	kyphosis	J:97104
	mandibular hyperostosis	J:97104
	osteoporosis	J:97104
	postnatal growth retardation	J:97104
	premature death	J:97104

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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