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ENRat
Rlbp1 - retinaldehyde binding protein 1
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Predicted to enable 11-cis retinal binding activity and phosphatidylinositol bisphosphate binding activity. Predicted to be involved in visual perception. Located in cell body. Human ortholog(s) of this gene implicated in Bothnia retinal dystrophy; Newfoundland cone-rod dystrophy; fundus albipunctatus; night blindness; and retinitis pigmentosa. Orthologous to human RLBP1 (retinaldehyde binding protein 1). [provided by Alliance of Genome Resources, Apr 2022]
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Basic Information
NCBI
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Rlbp1 Genetics information (-)
mRatBN7.2
Sequence Homology
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* This data comes from NCBI.
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