Slc13a4 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Slc13a4
solute carrier family 13 (sodium/sulfate symporters), member 4
MGI:2442367

21 phenotypes from 4 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Slc13a4^{em1(IMPC)Hmgu}/Slc13a4⁺ C57BL/6NCrl-Slc13a4^{em1(IMPC)Hmgu}/Ieg	abnormal bone structure	J:211773
Slc13a4^{em1(IMPC)Hmgu}/Slc13a4^{em1(IMPC)Hmgu} C57BL/6NCrl-Slc13a4^{em1(IMPC)Hmgu}/Ieg	preweaning lethality, complete penetrance	J:211773
Slc13a4^{tm1a(EUCOMM)Wtsi}/Slc13a4⁺ involves: C57BL/6J * C57BL/6N	abnormal thoracic cage morphology	J:239786
	decreased bone mineralization	J:239786
Slc13a4^{tm1a(EUCOMM)Wtsi}/Slc13a4^{tm1a(EUCOMM)Wtsi} involves: C57BL/6J * C57BL/6N	abnormal craniofacial morphology	J:239786
	abnormal developmental vascular remodeling	J:239786
	abnormal lens morphology	J:239786
	abnormal mineral level	J:239786
	abnormal palate development	J:239786
	abnormal placental transport	J:239786
	abnormal skeleton morphology	J:239786
	cleft palate	J:239786
	coloboma	J:239786
	failure of bone ossification	J:239786
	hemorrhage	J:239786
	iris coloboma	J:239786
	lethality throughout fetal growth and development, complete penetrance	J:239786
	pallor	J:239786
	subcutaneous edema	J:239786
Slc13a4^{tm1c(EUCOMM)Wtsi}/Slc13a4^{tm1d(EUCOMM)Wtsi} Edil3^{Tg(Sox2-cre)1Amc}/Edil3⁺ involves: C57BL/6 * CBA	normal embryo phenotype	J:239786
	lethality throughout fetal growth and development, complete penetrance	J:239786
	normal mortality/aging	J:239786
Slc13a4^{tm1d(EUCOMM)Wtsi}/Slc13a4^{tm1d(EUCOMM)Wtsi} involves: C57BL/6 * CBA	lethality throughout fetal growth and development, complete penetrance	J:239786

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