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ENRat
Ophn1 - oligophrenin 1
Alias:
Opn1
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Enables ionotropic glutamate receptor binding activity. Involved in maintenance of postsynaptic specialization structure. Is active in glutamatergic synapse. Human ortholog(s) of this gene implicated in X-linked mental retardation with cerebellar hypoplasia and distinctive facial appearance. Orthologous to human OPHN1 (oligophrenin 1). [provided by Alliance of Genome Resources, Apr 2022]
Basic Information
NCBI
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Ophn1 Genetics information (-)
mRatBN7.2
Sequence Homology
Transcripts & Proteins
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* This data comes from NCBI.
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