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Gene Expression Data
Assay Details
Assay
Reference: J:191149 Alves CH, et al., Loss of CRB2 in the mouse retina mimics human retinitis pigmentosa due to mutations in the CRB1 gene. Hum Mol Genet. 2013 Jan 1;22(1):35-50
Assay type: Immunohistochemistry
MGI Accession ID: MGI:7506993
Gene symbol: Opn1mw
Gene name: opsin 1 (cone pigments), medium-wave-sensitive (color blindness, deutan)
Antibody: anti-red/green Opsin (AB5405)
Detection system: Secondary antibody coupled to Alexa Fluor 488
Results
Specimen 7K: postnatal month 3; Crb2tm1.1Wij/? (more )
Note: Controls could be Crb2F/F or Crb2F/+/Chx10Cre+/-. Double labeled: green - Opn1mw; red - peanut agglutinin (PNA).
Structure Cell Type Level Pattern Image Note
TS28: photoreceptor layer retinal cone cell Present Regionally restricted 7K M-opsin staining was mainly in the segments of the photoreceptors.
Specimen 7L: postnatal month 3; Crb2tm1.1Wij/Crb2tm1.1Wij, Tg(Chx10-EGFP/cre,-ALPP)2Clc/0 (more )
Note: Conditional mutant. Double labeled: green - Opn1mw; red - peanut agglutinin (PNA).
Structure Cell Type Level Pattern Image Note
TS28: retina retinal cone cell Present Regionally restricted 7L Ectopic localization of M-opsin staining was noted in the cell bodies.
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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03/24/2026
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