Slc25a46 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Slc25a46
solute carrier family 25, member 46
MGI:1914703

27 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Slc25a46^atc/Slc25a46^atc B6.Cg-Slc25a46^atc	abnormal locomotor behavior	J:242350
	abnormal neuromuscular synapse morphology	J:242350
	abnormal node of Ranvier morphology	J:242350
	abnormal Purkinje cell dendrite morphology	J:242350
	abnormal Purkinje cell mitochondrial morphology	J:242350
	abnormal retina ganglion cell dendrite morphology	J:242350
	abnormal retina ganglion cell morphology	J:242350
	abnormal synapse morphology	J:242350
	astrocytosis	J:242350
	ataxia	J:242350
	cerebellum hypoplasia	J:242350
	decreased amacrine cell number	J:242350
	decreased grip strength	J:242350
	decreased spinal cord size	J:242350
	decreased spleen weight	J:242350
	decreased thymus weight	J:242350
	limb grasping	J:242350
	microgliosis	J:242350
	optic nerve atrophy	J:242350
	postnatal growth retardation	J:242350
	premature death	J:242350
	spleen hypoplasia	J:242350
	thin cerebellar molecular layer	J:242350
	thymus hypoplasia	J:242350
	tonic-clonic seizures	J:242350
Slc25a46^em1(IMPC)J/Slc25a46⁺ C57BL/6NJ-Slc25a46^em1(IMPC)J/J	decreased grip strength	J:211773
	increased circulating glucose level	J:211773
	increased fasting circulating glucose level	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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