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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Wdr48
WD repeat domain 48
MGI:1914811
14 phenotypes from 1 allele in 1 genetic background
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Allelic Composition
Genetic Background
Annotated Term Reference
Wdr48Gt(CSD197)Byg/Wdr48+
B6.129P2-Wdr48Gt(CSD197)Byg
abnormal seminiferous tubule morphology J:206106
abnormal skeleton morphology J:206106
abnormal skin physiology J:206106
abnormal spermatogenesis J:206106
decreased birth weight J:206106
decreased male germ cell number J:206106
decreased oocyte number J:206106
reduced female fertility J:206106
reduced male fertility J:206106
small testis J:206106
testicular atrophy J:206106
Wdr48Gt(CSD197)Byg/Wdr48Gt(CSD197)Byg
B6.129P2-Wdr48Gt(CSD197)Byg
embryonic growth retardation J:206106
embryonic lethality during organogenesis, complete penetrance J:206106
embryonic lethality, incomplete penetrance J:206106

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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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory