MGI MP annotations for MGI:1321392: Pex7

Gray arrows indicate "is_a"



Compare annotations to MP categories for MGI:1321392.

• Entry indicates phenotypic allele for this gene.
• Colored entries indicate MP annotation.

ID	Term	Pex7tm1Nbra	Pex7tm1Rjaw
MP:0005386	behavior/neurological phenotype	Pex7tm1Nbra	Pex7tm1Rjaw
MP:0005385	cardiovascular system phenotype	Pex7tm1Nbra	Pex7tm1Rjaw
MP:0005384	cellular phenotype	Pex7tm1Nbra	Pex7tm1Rjaw
MP:0005379	endocrine/exocrine gland phenotype	Pex7tm1Nbra	Pex7tm1Rjaw
MP:0005378	growth/size phenotype	Pex7tm1Nbra	Pex7tm1Rjaw
MP:0005397	hematopoietic system phenotype	Pex7tm1Nbra	Pex7tm1Rjaw
MP:0005376	homeostasis/metabolism phenotype	Pex7tm1Nbra	Pex7tm1Rjaw
MP:0005387	immune system phenotype	Pex7tm1Nbra	Pex7tm1Rjaw
MP:0005370	liver/biliary system phenotype	Pex7tm1Nbra	Pex7tm1Rjaw
MP:0010768	mortality/aging	Pex7tm1Nbra	Pex7tm1Rjaw
MP:0005369	muscle phenotype	Pex7tm1Nbra	Pex7tm1Rjaw
MP:0003631	nervous system phenotype	Pex7tm1Nbra	Pex7tm1Rjaw
MP:0005389	reproductive system phenotype	Pex7tm1Nbra	Pex7tm1Rjaw
MP:0005390	skeleton phenotype	Pex7tm1Nbra	Pex7tm1Rjaw
MP:0005391	vision/eye phenotype	Pex7tm1Nbra	Pex7tm1Rjaw

Full set of annotations for MGI:1321392

ID	Term	Allele	Alleles	Background	Color Key
MP:0000639	abnormal adrenal gland morphology	Pex7tm1Nbra	Pex7tm1Nbra/Pex7tm1Nbra	involves: 129S/SvEv * C57BL/6	color key
MP:0002896	abnormal bone mineralization	Pex7tm1Rjaw	Pex7tm1Rjaw/Pex7tm1Rjaw	Swiss	color key
MP:0000164	abnormal cartilage development	Pex7tm1Rjaw	Pex7tm1Rjaw/Pex7tm1Rjaw	Swiss	color key
MP:0005621	abnormal cell physiology	Pex7tm1Nbra	Pex7tm1Nbra/Pex7tm1Nbra	involves: 129S/SvEv * C57BL/6	color key
MP:0000788	abnormal cerebral cortex morphology	Pex7tm1Rjaw	Pex7tm1Rjaw/Pex7tm1Rjaw	Swiss	color key
MP:0001431	abnormal eating behavior	Pex7tm1Rjaw	Pex7tm1Rjaw/Pex7tm1Rjaw	Swiss	color key
MP:0005584	abnormal enzyme/coenzyme activity	Pex7tm1Nbra	Pex7tm1Nbra/Pex7tm1Nbra	involves: 129S/SvEv * C57BL/6	color key
MP:0000266	abnormal heart morphology	Pex7tm1Nbra	Pex7tm1Nbra/Pex7tm1Nbra	involves: 129S/SvEv * C57BL/6	color key
MP:0000807	abnormal hippocampus morphology	Pex7tm1Nbra	Pex7tm1Nbra/Pex7tm1Nbra	involves: 129S/SvEv * C57BL/6	color key
MP:0003236	abnormal lens capsule morphology	Pex7tm1Nbra	Pex7tm1Nbra/Pex7tm1Nbra	involves: 129S/SvEv * C57BL/6	color key
MP:0002840	abnormal lens fiber morphology	Pex7tm1Nbra	Pex7tm1Nbra/Pex7tm1Nbra	involves: 129S/SvEv * C57BL/6	color key
MP:0001303	abnormal lens morphology	Pex7tm1Nbra	Pex7tm1Nbra/Pex7tm1Nbra	involves: 129S/SvEv * C57BL/6	color key
MP:0001547	abnormal lipid level	Pex7tm1Rjaw	Pex7tm1Rjaw/Pex7tm1Rjaw	Swiss	color key
MP:0006009	abnormal neuronal migration	Pex7tm1Rjaw	Pex7tm1Rjaw/Pex7tm1Rjaw	Swiss	color key
MP:0004982	abnormal osteoclast morphology	Pex7tm1Rjaw	Pex7tm1Rjaw/Pex7tm1Rjaw	Swiss	color key
MP:0000955	abnormal spinal cord morphology	Pex7tm1Nbra	Pex7tm1Nbra/Pex7tm1Nbra	involves: 129S/SvEv * C57BL/6	color key
MP:0001304	cataracts	Pex7tm1Nbra	Pex7tm1Nbra/Pex7tm1Nbra	involves: 129S/SvEv * C57BL/6	color key
MP:0001304	cataracts	Pex7tm1Rjaw	Pex7tm1Rjaw/Pex7tm1Rjaw	Swiss	color key
MP:0009703	decreased birth body size	Pex7tm1Nbra	Pex7tm1Nbra/Pex7tm1Nbra	involves: 129S/SvEv * C57BL/6	color key
MP:0009674	decreased birth weight	Pex7tm1Nbra	Pex7tm1Nbra/Pex7tm1Nbra	involves: 129S/SvEv * C57BL/6	color key
MP:0001265	decreased body size	Pex7tm1Nbra	Pex7tm1Nbra/Pex7tm1Nbra	involves: 129S/SvEv * C57BL/6	color key
MP:0001262	decreased body weight	Pex7tm1Nbra	Pex7tm1Nbra/Pex7tm1Nbra	involves: 129S/SvEv * C57BL/6	color key
MP:0001262	decreased body weight	Pex7tm1Rjaw	Pex7tm1Rjaw/Pex7tm1Rjaw	Swiss	color key
MP:0005282	decreased fatty acid level	Pex7tm1Nbra	Pex7tm1Nbra/Pex7tm1Nbra	involves: 129S/SvEv * C57BL/6	color key
MP:0001935	decreased litter size	Pex7tm1Nbra	Pex7tm1Nbra/Pex7tm1Nbra	involves: 129S/SvEv * C57BL/6	color key
MP:0005286	decreased saturated fatty acid level	Pex7tm1Nbra	Pex7tm1Nbra/Pex7tm1Nbra	involves: 129S/SvEv * C57BL/6	color key
MP:0000060	delayed bone ossification	Pex7tm1Nbra	Pex7tm1Nbra/Pex7tm1Nbra	involves: 129S/SvEv * C57BL/6	color key
MP:0000921	demyelination	Pex7tm1Nbra	Pex7tm1Nbra/Pex7tm1Nbra	involves: 129S/SvEv * C57BL/6	color key
MP:0002427	disproportionate dwarf	Pex7tm1Rjaw	Pex7tm1Rjaw/Pex7tm1Rjaw	Swiss	color key
MP:0005323	dystonia	Pex7tm1Rjaw	Pex7tm1Rjaw/Pex7tm1Rjaw	Swiss	color key
MP:0000599	enlarged liver	Pex7tm1Nbra	Pex7tm1Nbra/Pex7tm1Nbra	involves: 129S/SvEv * C57BL/6	color key
MP:0002628	hepatic steatosis	Pex7tm1Nbra	Pex7tm1Nbra/Pex7tm1Nbra	involves: 129S/SvEv * C57BL/6	color key
MP:0005281	increased fatty acid level	Pex7tm1Nbra	Pex7tm1Nbra/Pex7tm1Nbra	involves: 129S/SvEv * C57BL/6	color key
MP:0005281	increased fatty acid level	Pex7tm1Rjaw	Pex7tm1Rjaw/Pex7tm1Rjaw	Swiss	color key
MP:0009763	increased sensitivity to induced morbidity/mortality	Pex7tm1Nbra	Pex7tm1Nbra/Pex7tm1Nbra	involves: 129S/SvEv * C57BL/6	color key
MP:0010180	increased susceptibility to weight loss	Pex7tm1Nbra	Pex7tm1Nbra/Pex7tm1Nbra	involves: 129S/SvEv * C57BL/6	color key
MP:0001924	infertility	Pex7tm1Rjaw	Pex7tm1Rjaw/Pex7tm1Rjaw	Swiss	color key
MP:0008570	lipidosis	Pex7tm1Nbra	Pex7tm1Nbra/Pex7tm1Nbra	involves: 129S/SvEv * C57BL/6	color key
MP:0003103	liver degeneration	Pex7tm1Nbra	Pex7tm1Nbra/Pex7tm1Nbra	involves: 129S/SvEv * C57BL/6	color key
MP:0001860	liver inflammation	Pex7tm1Nbra	Pex7tm1Nbra/Pex7tm1Nbra	involves: 129S/SvEv * C57BL/6	color key
MP:0011088	partial neonatal lethality	Pex7tm1Rjaw	Pex7tm1Rjaw/Pex7tm1Rjaw	Swiss	color key
MP:0001921	reduced fertility	Pex7tm1Nbra	Pex7tm1Nbra/Pex7tm1Nbra	involves: 129S/SvEv * C57BL/6	color key
MP:0008489	slow postnatal weight gain	Pex7tm1Nbra	Pex7tm1Nbra/Pex7tm1Nbra	involves: 129S/SvEv * C57BL/6	color key
MP:0003205	testicular atrophy	Pex7tm1Rjaw	Pex7tm1Rjaw/Pex7tm1Rjaw	Swiss	color key