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Symbol
Name
ID

Arl13b
ADP-ribosylation factor-like 13B
MGI:1915396

Phenotype annotations related to vision/eye

Darker colors indicate more annotations

Human Phenotypes	Optic disc pallor	Pigmentary retinopathy	Oculomotor apraxia	Ptosis
Disease(s) Associated with ARL13B
Joubert syndrome 8

Mouse Phenotypes		abnormal photoreceptor connecting cilium morphology	short photoreceptor inner segment	abnormal photoreceptor outer segment morphology	abnormal photoreceptor outer segment disc membrane morphology	short photoreceptor outer segment	retina photoreceptor degeneration	abnormal retina development	abnormal ocular fundus morphology	decreased total retina thickness	abnormal electroretinogram waveform feature
Availability	Mouse Genotype	abnormal photoreceptor connecting cilium morphology	short photoreceptor inner segment	abnormal photoreceptor outer segment morphology		short photoreceptor outer segment	retina photoreceptor degeneration	abnormal retina development	abnormal ocular fundus morphology	decreased total retina thickness	abnormal electroretinogram waveform feature
	Arl13b^tm1.1Tc/Arl13b^tm1.1Tc Tg(Six3-cre)69Frty/0 (conditional)
	Arl13b^tm1.1Tc/Arl13b^tm1.1Tc Pde6g^{tm1(cre/ERT2)Eye}/Pde6g⁺ (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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