Slc19a1 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Slc19a1
solute carrier family 19 (folate transporter), member 1
MGI:103182

21 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Slc19a1^tm1Gold/Slc19a1^tm1Gold involves: 129/Sv * C57BL/6 * SJL	abnormal erythropoiesis	J:68666
	abnormal hematopoietic system morphology/development	J:68666
	abnormal kidney development	J:68666
	abnormal lymphopoiesis	J:68666
	abnormal seminiferous tubule morphology	J:68666
	decreased body weight	J:68666
	decreased lymphocyte cell number	J:68666
	embryonic growth retardation	J:68666
	embryonic lethality, complete penetrance	J:68666
	impaired hematopoiesis	J:68666
	pale liver	J:68666
	pallor	J:68666
	postnatal growth retardation	J:68666
	postnatal lethality, complete penetrance	J:68666
	small spleen	J:68666
	small thymus	J:68666
Slc19a1^tm1Rsc/Slc19a1⁺ involves: 129P2/OlaHsd * SWV/Fnn	abnormal colon morphology	J:96380
	abnormal crypts of Lieberkuhn morphology	J:96380
	abnormal homeostasis	J:96380
	increased physiological sensitivity to xenobiotic	J:96380
Slc19a1^tm1Rsc/Slc19a1^tm1Rsc involves: 129P2/OlaHsd * SWV/Fnn	prenatal lethality, complete penetrance	J:96380

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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