Helt Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Helt
helt bHLH transcription factor
MGI:3040955

11 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Helt^tm1Wrst/Helt^tm1Wrst B6.Cg-Helt^tm1Wrst	abnormal suckling behavior	J:119562
	decreased body weight	J:119562
	limb grasping	J:119562
	loss of GABAergic neurons	J:119562
	normal nervous system phenotype	J:119562
	postnatal growth retardation	J:119562
	postnatal lethality, incomplete penetrance	J:119562
	premature death	J:119562
	seizures	J:119562
	tonic-clonic seizures	J:119562
Helt^tm1Yono/Helt^tm1Yono involves: 129S/SvEv * C57BL/6	abnormal glutaminergic neuron morphology	J:124115
Helt^tm1Yono/Helt^tm1Yono involves: 129S/SvEv * C57BL/6	loss of GABAergic neurons	J:124115

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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