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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID 		P3h2tm1d(KOMP)Wtsi
targeted mutation 1d, Wellcome Trust Sanger Institute
MGI:5792811
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
 		P3h2tm1d(KOMP)Wtsi/P3h2tm1d(KOMP)Wtsi involves: C57BL/6J * C57BL/6N MGI:6191778


Genotype
MGI:6191778
hm1
Allelic
Composition		 P3h2tm1d(KOMP)Wtsi/P3h2tm1d(KOMP)Wtsi
Genetic
Background		 involves: C57BL/6J * C57BL/6N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
P3h2tm1d(KOMP)Wtsi mutation (0 available); any P3h2 mutation (37 available)
♀ phenotype observed in females
♂ phenotype observed in males
N normal phenotype
skeleton
skeleton phenotype ( J:220554 )
N
• mice exhibit normal skeletal phenotypes

vision/eye
abnormal eye physiology ( J:220554 )
• collagens I and IV from eye tissues are reduced in 3-hyroxylation




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
10/07/2025
MGI 6.24 		The Jackson Laboratory