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Symbol
Name
ID

Ttll5
tubulin tyrosine ligase-like family, member 5
MGI:2443657

Phenotype annotations related to vision/eye

*	Aspects of the system are reported to show a normal phenotype.
	Darker colors indicate more annotations

Human Phenotypes	Cone/cone-rod dystrophy	Perifoveal ring of hyperautofluorescence	Undetectable pattern electroretinogram	High myopia	Reduced visual acuity
Disease(s) Associated with TTLL5
cone-rod dystrophy 19

Mouse Phenotypes		vision/eye phenotype	abnormal retina cone cell morphology	abnormal ocular fundus morphology	thin retina outer nuclear layer	retina degeneration	decreased a-wave amplitude	decreased b-wave amplitude
Availability	Mouse Genotype
	Ttll5^tm1.1N/Ttll5^tm1.1N	*

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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