Slc25a1 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Slc25a1
solute carrier family 25 (mitochondrial carrier, citrate transporter), member 1
MGI:1345283

25 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Slc25a1^{em1(IMPC)Kmpc}/Slc25a1⁺ C57BL/6NTac-Slc25a1^{em1(IMPC)Kmpc}/Kmpc	decreased blood urea nitrogen level	J:211773
	no spontaneous movement	J:211773
Slc25a1^{em1(IMPC)Kmpc}/Slc25a1^{em1(IMPC)Kmpc} C57BL/6NTac-Slc25a1^{em1(IMPC)Kmpc}/Kmpc	abnormal embryo size	J:211773
	abnormal tail morphology	J:211773
	edema	J:211773
	embryonic growth retardation	J:211773
	no spontaneous movement	J:211773
	preweaning lethality, complete penetrance	J:211773
Slc25a1^{tm1b(EUCOMM)Wtsi}/Slc25a1⁺ C57BL/6N-Slc25a1^{tm1b(EUCOMM)Wtsi}/Bay	abnormal retina vasculature morphology	J:211773
	increased exploration in new environment	J:211773
Slc25a1^{tm1b(EUCOMM)Wtsi}/Slc25a1^{tm1b(EUCOMM)Wtsi} C57BL/6N-Slc25a1^{tm1b(EUCOMM)Wtsi}/Bay	abnormal craniofacial morphology	J:211773
	abnormal cranium morphology	J:211773
	abnormal ear morphology	J:211773
	abnormal embryo development	J:211773
	abnormal embryo size	J:211773
	abnormal facial morphology	J:211773
	abnormal forebrain morphology	J:211773
	abnormal head shape	J:211773
	abnormal head size	J:211773
	abnormal hindbrain morphology	J:211773
	abnormal limb morphology	J:211773
	abnormal neural tube closure	J:211773
	anophthalmia	J:211773
	embryonic growth retardation	J:211773
	exencephaly	J:211773
	facial cleft	J:211773
	pallor	J:211773
	preweaning lethality, complete penetrance	J:211773
	protruding tongue	J:211773

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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