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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID 		PdgfcGt(OST91573)Lex
gene trap OST91573, Lexicon Genetics
MGI:3530825
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
 		PdgfcGt(OST91573)Lex/PdgfcGt(OST91573)Lex involves: 129S5/SvEvBrd * C57BL/6J MGI:3609817


Genotype
MGI:3609817
hm1
Allelic
Composition		 PdgfcGt(OST91573)Lex/PdgfcGt(OST91573)Lex
Genetic
Background		 involves: 129S5/SvEvBrd * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
PdgfcGt(OST91573)Lex mutation (3 available); any Pdgfc mutation (35 available)
♀ phenotype observed in females
♂ phenotype observed in males
N normal phenotype
vision/eye
abnormal retina pigmentation ( J:171883 )
• depigmented spots are seen in the retina

pigmentation
abnormal retina pigmentation ( J:171883 )
• depigmented spots are seen in the retina




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