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Symbol
Name
ID

Acvrl1
activin A receptor, type II-like 1
MGI:1338946

Phenotype annotations related to nervous system

Darker colors indicate more annotations

Human Phenotypes	Cerebral hemorrhage	Subarachnoid hemorrhage	Cerebral arteriovenous malformation	Spinal arteriovenous malformation	Abnormal cerebral vascular morphology	Ischemic stroke	Transient ischemic attack	Brain abscess	Migraine	Seizure
Disease(s) Associated with ACVRL1
hereditary hemorrhagic telangiectasia

Mouse Phenotypes		abnormal brain vasculature morphology	cerebral arteriovenous malformation	dilated brain ventricle	abnormal cholinergic neuron morphology	abnormal sympathetic nervous system physiology
Availability	Mouse Genotype	abnormal brain vasculature morphology	cerebral arteriovenous malformation	dilated brain ventricle	abnormal cholinergic neuron morphology	abnormal sympathetic nervous system physiology
	Acvrl1^tm1Enl/Acvrl1⁺
	Acvrl1^tm2.1Spo/Acvrl1^tm2.1Spo Tg(Acvrl1-cre)L1Spo/0 (conditional)
	Acvrl1^tm2.1Spo/Acvrl1^tm2.1Spo (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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