Phenotypes for C1qtnf5 MGI:5309011 MGI Mouse

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Phenotypes Associated with This Genotype

Allelic Composition	C1qtnf5^tm1.1Geno/C1qtnf5^tm1.1Geno
Genetic Background	involves: 129 * C57BL/6J

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Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
C1qtnf5^tm1.1Geno 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 (C1qtnf5^tm1.1Itl), 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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