Hnrnpa1 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Hnrnpa1
heterogeneous nuclear ribonucleoprotein A1
MGI:104820

13 phenotypes from 1 allele in 1 genetic background

Allelic Composition Genetic Background	Annotated Term	Reference
Hnrnpa1^tm1.1Cyf/Hnrnpa1⁺ involves: 129S1/Sv * 129X1/SvJ * C57BL/6JNarl	abnormal P wave	J:238260
	increased heart rate	J:238260
	increased systemic arterial systolic blood pressure	J:238260
	shortened PR interval	J:238260
Hnrnpa1^tm1.1Cyf/Hnrnpa1^tm1.1Cyf involves: 129S1/Sv * 129X1/SvJ * C57BL/6JNarl	abnormal intercostal muscle morphology	J:238260
	abnormal tongue muscle morphology	J:238260
	abnormal urinary bladder morphology	J:238260
	decreased body length	J:238260
	dilated cardiomyopathy	J:238260
	dilated heart ventricle	J:238260
	neonatal lethality, complete penetrance	J:238260
	prenatal lethality, incomplete penetrance	J:238260
	tongue muscle hypoplasia	J:238260

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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