Fryl Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Fryl
FRY like transcription coactivator
MGI:1919563

26 phenotypes from 3 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Fryl^{Gt(Ayu21-T312)Imeg}/Fryl^{Gt(Ayu21-T312)Imeg} B6J.Cg-Fryl^{Gt(Ayu21-T312)Imeg}	abnormal kidney collecting duct morphology	J:260667
	abnormal kidney development	J:260667
	abnormal renal tubule morphology	J:260667
	decreased body weight	J:260667
	dilated kidney collecting duct	J:260667
	enlarged kidney	J:260667
	hydronephrosis	J:260667
	increased kidney apoptosis	J:260667
	kidney cortex cyst	J:260667
	kidney cyst	J:260667
	kidney inflammation	J:260667
	kidney medulla cyst	J:260667
	pale kidney	J:260667
	postnatal growth retardation	J:260667
	postnatal lethality, incomplete penetrance	J:260667
	premature death	J:260667
	renal interstitial fibrosis	J:260667
Fryl^{tm1a(KOMP)Wtsi}/Fryl⁺ C57BL/6N-Fryl^{tm1a(KOMP)Wtsi}/Wtsi	abnormal skin pigmentation	J:175295
Fryl^{tm1b(KOMP)Wtsi}/Fryl⁺ C57BL/6N-Fryl^{tm1b(KOMP)Wtsi}/Wtsi	decreased circulating calcium level	J:211773
	increased mean corpuscular hemoglobin	J:211773
Fryl^{tm1b(KOMP)Wtsi}/Fryl^{tm1b(KOMP)Wtsi} C57BL/6N-Fryl^{tm1b(KOMP)Wtsi}/Wtsi	abnormal placenta morphology	J:261316
	abnormal placental labyrinth vasculature morphology	J:261316
	lethality throughout fetal growth and development, incomplete penetrance	J:261316
	placenta hemorrhage	J:261316
	placenta necrosis	J:261316
	small placenta	J:261316

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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