Slc1a1 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Slc1a1
solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 1
MGI:105083

13 phenotypes from 2 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Slc1a1^{tm1b(KOMP)Wtsi}/Slc1a1^{tm1b(KOMP)Wtsi} C57BL/6N-Slc1a1^{tm1b(KOMP)Wtsi}/J	fused cornea and lens	J:211773
	increased circulating iron level	J:211773
	increased circulating sodium level	J:211773
	increased exploration in new environment	J:211773
	increased vertical activity	J:211773
Slc1a1^tm1Wst/Slc1a1^tm1Wst B6.129-Slc1a1^tm1Wst	decreased retina ganglion cell number	J:124191
	increased cellular sensitivity to hydrogen peroxide	J:124191
	increased lactate dehydrogenase level	J:124191
	optic nerve degeneration	J:124191
	normal vision/eye phenotype	J:124191
Slc1a1^tm1Wst/Slc1a1^tm1Wst involves: 129S1/Sv * 129X1/SvJ * C57BL/6	normal behavior/neurological phenotype	J:41613
	decreased locomotor activity	J:41613
	dicarboxylic aciduria	J:41613

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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