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Symbol
Name
ID
Emc1
ER membrane protein complex subunit 1
MGI:2443696
Phenotype annotations related to vision/eye
Darker colors indicate more annotations
Human Phenotypes
Astigmatism
Optic atrophy
Deeply set eye
Hypertelorism
Abnormal electroretinogram
Abnormality of visual evoked potentials
Strabismus
Esotropia
Hypermetropia
Myopia
Cerebral visual impairment
Disease(s) Associated with EMC1
cerebellar atrophy, visual impairment, and psychomotor retardation

Mouse Phenotypes
increased retina apoptosis
decreased retina cone cell number
abnormal photoreceptor outer segment morphology
short photoreceptor outer segment
disorganized photoreceptor outer segment
photoreceptor outer segment degeneration
abnormal retina cone cell morphology
retina cone cell degeneration
retina photoreceptor degeneration
thin retina outer nuclear layer
abnormal retina photoreceptor layer morphology
decreased a-wave amplitude
decreased b-wave amplitude
abnormal rod electrophysiology
Availability Mouse Genotype
Emc1em1Xjz/Emc1em1Xjz
Tg(OPN1LW-cre)4Yzl/0  (conditional)
Emc1em1Xjz/Emc1em1Xjz
Tg(Rho-icre)1Ck/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)
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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory