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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID 		C1qtnf5tm1.1Geno
targeted mutation 1.1, Genoway
MGI:5309003
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
 		C1qtnf5tm1.1Geno/C1qtnf5tm1.1Geno involves: 129 * C57BL/6J MGI:5309011


Genotype
MGI:5309011
hm1
Allelic
Composition		 C1qtnf5tm1.1Geno/C1qtnf5tm1.1Geno
Genetic
Background		 involves: 129 * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
C1qtnf5tm1.1Geno mutation (0 available); any C1qtnf5 mutation (14 available)
♀ phenotype observed in females
♂ phenotype observed in males
N normal phenotype
normal phenotype
no abnormal phenotype detected ( J:180961 )
• in contrast to a previously generated Ser163Arg knock-in (C1qtnf5tm1.1Itl), mice exhibit no significant abnormalities (including normal eye morphology)

Mouse Models of Human Disease
 DO ID OMIM ID(s) Ref(s)
NOT late-onset retinal degeneration DOID:0060869 OMIM:605670
 J:180961




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
11/12/2024
MGI 6.24 		The Jackson Laboratory