Supt20 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Supt20
SPT20 SAGA complex component
MGI:1929651

22 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Supt20^drey/Supt20^drey either: C3.B6-Supt20^drey or (involves: C3H/HeJ * C57BL/6J)	abnormal allantois morphology	J:106348
	abnormal gastrulation movements	J:106348
	abnormal mesoderm development	J:106348
	abnormal retina pigment epithelium morphology	J:106348
	abnormal somite development	J:106348
	caudal body truncation	J:106348
	embryonic growth retardation	J:106348
	exencephaly	J:106348
	failure of initiation of embryo turning	J:106348
	open neural tube	J:106348
	prenatal lethality, incomplete penetrance	J:106348
	spina bifida	J:106348
Supt20^{Gt(RRK304)Byg}/Supt20^{Gt(RRK304)Byg} involves: 129P2/OlaHsd	abnormal allantois morphology	J:106348
	abnormal developmental patterning	J:106348
	abnormal head fold morphology	J:106348
	abnormal left-right axis symmetry of the somites	J:106348
	abnormal mesoderm development	J:106348
	abnormal paraxial mesoderm morphology	J:106348
	abnormal primitive streak morphology	J:106348
	abnormal visceral yolk sac morphology	J:106348
	abnormal vitelline vasculature morphology	J:106348
	embryo tissue necrosis	J:106348
	embryonic growth retardation	J:106348
	exencephaly	J:106348
	failure of chorioallantoic fusion	J:106348
	incomplete somite formation	J:106348

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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