Fezf2 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Fezf2
Fez family zinc finger 2
MGI:1859823

17 phenotypes from 5 alleles in 7 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Fezf2^tm1.1Nses/Fezf2^tm1.1Nses Emx1^tm1(cre)Ito/Emx1⁺ involves: 129P2/OlaHsd * 129S1/Sv	abnormal corticospinal tract morphology	J:186632
Fezf2^tm1.1Nses/Fezf2^tm1.1Nses Tg(CAG-cat,-EGFP)39Miya/0 Tg(Emx1-cre)#Ito/0 involves: 129S1/Sv * C57BL/6 * C57BL/6NJcl * DBA/2NJcl	abnormal corticospinal tract morphology	J:169221
Fezf2^tm1Hibi/Fezf2^tm1Hibi involves: 129S1/Sv * 129X1/SvJ	abnormal axon guidance	J:214959
Fezf2^tm1Hibi/Fezf2^tm1Hibi involves: 129S1/Sv * 129X1/SvJ	increased anterior commissure size	J:214959
Fezf2^tm1Hibi/Fezf2^tm1Hibi involves: 129S1/Sv * 129X1/SvJ * C57BL/6	abnormal food preference	J:91247
	abnormal stationary movement	J:91247
	abnormal telencephalon development	J:91247
	abnormal thalamus morphology	J:91247
	hyperactivity	J:91247
	postnatal growth retardation	J:91247
	premature death	J:91247
Fezf2^tm1Skm/Fezf2^tm1Skm involves: 129	abnormal vomeronasal organ morphology	J:174726
	abnormal vomeronasal sensory neuron morphology	J:174726
	small vomeronasal organ	J:174726
Fezf2^tm1Skm/Fezf2^tm1Skm involves: 129 * CD-1	abnormal axon guidance	J:103829
	abnormal axon morphology	J:103829
	abnormal cerebral cortex morphology	J:103829
	absent corpus callosum	J:103829
Tg(Fezf2,-Venus)1Hibi/? Not Specified	abnormal diencephalon morphology	J:119561
Tg(Otx2-Fezf2,Venus)1Hibi/? Not Specified	abnormal diencephalon morphology	J:119561

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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