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Symbol
Name
ID

Arl3
ADP-ribosylation factor-like 3
MGI:1929699

Phenotype annotations related to nervous system

Darker colors indicate more annotations

Human Phenotypes

Encephalocele

Aganglionic megacolon

Oculomotor apraxia

Hydrocephalus

Polymicrogyria

Aplasia/Hypoplasia of the corpus callosum

Cerebellar vermis hypoplasia

Abnormality of neuronal migration

Ataxia

Tremor

Intellectual disability

Gait disturbance

Global developmental delay

Seizure

Disease(s) Associated with ARL3

Joubert syndrome

Mouse Phenotypes		abnormal photoreceptor connecting cilium morphology	abnormal photoreceptor inner segment morphology	abnormal photoreceptor outer segment morphology	absent photoreceptor outer segment	short photoreceptor outer segment	abnormal retina rod cell outer segment morphology	retina cone cell degeneration	abnormal retina rod cell morphology	retina rod cell degeneration
Availability	Mouse Genotype	abnormal photoreceptor connecting cilium morphology	abnormal photoreceptor inner segment morphology	abnormal photoreceptor outer segment morphology	absent photoreceptor outer segment	short photoreceptor outer segment	abnormal retina rod cell outer segment morphology	retina cone cell degeneration	abnormal retina rod cell morphology	retina rod cell degeneration
	Arl3^{Gt(OST263303)Lex}/Arl3^{Gt(OST263303)Lex}
	Tg(Rho-Arl3*Q71L)#Visu/0
	Arl3^{Gt(EUCJ0159b07)1.1Hmgu}/Arl3^{Gt(EUCJ0159b07)1.1Hmgu} Tg(Rho-icre)1Ck/0 (conditional)
	Arl3^{Gt(EUCJ0159b07)1.1Hmgu}/Arl3^{Gt(EUCJ0159b07)1.1Hmgu} Tg(Six3-cre)69Frty/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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 04/23/2024 MGI 6.23