Tmsb4x Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Tmsb4x
thymosin, beta 4, X chromosome
MGI:99510

21 phenotypes from 5 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Tmsb4x^em1(IMPC)Mbp/Y C57BL/6NCrl-Tmsb4x^em1(IMPC)Mbp/MbpMmucd	increased vertical activity	J:211773
Tmsb4x^em1(IMPC)Mbp/Tmsb4x^em1(IMPC)Mbp C57BL/6NCrl-Tmsb4x^em1(IMPC)Mbp/MbpMmucd	abnormal behavior	J:211773
	abnormal skin morphology	J:211773
	abnormal spleen morphology	J:211773
	decreased anxiety-related response	J:211773
	decreased locomotor activity	J:211773
	decreased thigmotaxis	J:211773
	enlarged spleen	J:211773
Tmsb4x^tm1.1Chen/Y involves: 129S1/Sv * 129X1/SvJ * Black Swiss	normal cardiovascular system phenotype	J:185264
	no abnormal phenotype detected	J:185264
Tmsb4x^tm1.1Chen/Tmsb4x^tm1.1Chen involves: 129S1/Sv * 129X1/SvJ * Black Swiss	normal cardiovascular system phenotype	J:185264
	no abnormal phenotype detected	J:185264
Tmsb4x^tm1.2Chen/Y Tg(Myhca-cre)1Abel/0 involves: 129S1/Sv * 129X1/SvJ * Black Swiss	no abnormal phenotype detected	J:185264
Tmsb4x^tm1.2Chen/Y Tg(Nkx2-5-cre)9Eno/0 involves: 129S1/Sv * 129X1/SvJ * Black Swiss	no abnormal phenotype detected	J:185264
Tmsb4x^tm1Chen/Tmsb4x^tm1Chen involves: 129S1/Sv * 129X1/SvJ * Black Swiss	no abnormal phenotype detected	J:185264
Tmsb4x^tm1Prri/Y B6.129-Tmsb4x^tm1Prri	embryonic lethality during organogenesis, incomplete penetrance	J:195902
Tmsb4x^tm1Prri/Tmsb4x^tm1Prri B6.129-Tmsb4x^tm1Prri	abnormal arteriole morphology	J:195902
	abnormal blood vessel morphology	J:195902
	abnormal vascular smooth muscle development	J:195902
	embryonic lethality during organogenesis, incomplete penetrance	J:195902
	heart hemorrhage	J:195902
	hemopericardium	J:195902
	internal hemorrhage	J:195902
	intracranial hemorrhage	J:195902
	thin myocardium	J:195902
	normal vision/eye phenotype	J:195902
Hprt1/Hprt1⁺ Tg(Tek-cre)1Ywa/0 involves: C57BL/6 * SJL	abnormal blood vessel morphology	J:195902
	embryonic lethality during organogenesis, incomplete penetrance	J:195902
	hemopericardium	J:195902
	internal hemorrhage	J:195902
	intracranial hemorrhage	J:195902
	lethality throughout fetal growth and development, incomplete penetrance	J:195902

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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