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Symbol
Name
ID

Dmxl2
Dmx-like 2
MGI:2444630

Phenotype annotations related to nervous system

Darker colors indicate more annotations

Human Phenotypes	EEG with burst suppression	Intellectual disability, profound	Global developmental delay	Peripheral neuropathy	Focal clonic seizure	Infantile spasms	Myoclonic seizure	Tonic seizure
Disease(s) Associated with DMXL2
developmental and epileptic encephalopathy 81

Mouse Phenotypes		multiple persisting craniopharyngeal ducts	abnormal hypothalamus morphology	abnormal hypothalamus secretion
Availability	Mouse Genotype	multiple persisting craniopharyngeal ducts	abnormal hypothalamus morphology	abnormal hypothalamus secretion
	Dmxl2^{tm1a(EUCOMM)Wtsi}/Dmxl2^{tm1a(EUCOMM)Wtsi}
	Dmxl2^{tm1c(EUCOMM)Wtsi}/Dmxl2⁺ Tg(Nes-cre)1Atp/0 (conditional)

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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