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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID 		Epha7tm1Ud
targeted mutation 1, Uwe Drescher
MGI:3583808
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
 		Epha7tm1Ud/Epha7tm1Ud involves: 129S1/Sv * 129X1/SvJ * C57BL/6 MGI:3584124


Genotype
MGI:3584124
hm1
Allelic
Composition		 Epha7tm1Ud/Epha7tm1Ud
Genetic
Background		 involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Epha7tm1Ud mutation (1 available); any Epha7 mutation (58 available)
♀ phenotype observed in females
♂ phenotype observed in males
N normal phenotype
nervous system
abnormal axon morphology ( J:99629 )
• the retinocollicular map is disrupted with nasal and temporal axons forming additional or extended termination zones, respectively




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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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory