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Symbol
Name
ID

Fa2h
fatty acid 2-hydroxylase
MGI:2443327

Phenotype annotations related to vision/eye

Darker colors indicate more annotations

Human Phenotypes	Optic atrophy	Strabismus	Nystagmus	Oculomotor apraxia	Ophthalmoplegia	External ophthalmoplegia
Disease(s) Associated with FA2H
hereditary spastic paraplegia 35

Mouse Phenotypes		abnormal optic nerve morphology	abnormal eye morphology	cataract	abnormal retina morphology	abnormal vitreous body morphology
Availability	Mouse Genotype	abnormal optic nerve morphology	abnormal eye morphology	cataract	abnormal retina morphology	abnormal vitreous body morphology
	Fa2h^em1(IMPC)Mbp/Fa2h^em1(IMPC)Mbp
	Fa2h^tm1.1Hama/Fa2h^tm1.1Hama

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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