RecName: Full=Calcium-binding protein 4; Short=CaBP4

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Retinal findings in a patient of French ancestry with CABP4-related retinal disease. [Doc Ophthalmol. 2018]
Retinal findings in a patient of French ancestry with CABP4-related retinal disease.
Smirnov VM, Zeitz C, Soumittra N, Audo I, Defoort-Dhellemmes S. Doc Ophthalmol. 2018 Apr; 136(2):135-143. Epub 2018 Mar 10.
Multimodal imaging in CABP4-related retinopathy. [Ophthalmic Genet. 2017]
Multimodal imaging in CABP4-related retinopathy.
Schatz P, Abdalla Elsayed MEA, Khan AO. Ophthalmic Genet. 2017 Sep-Oct; 38(5):459-464. Epub 2017 Mar 1.
CABP4 mutations do not cause congenital stationary night blindness. [Ophthalmology. 2014]
CABP4 mutations do not cause congenital stationary night blindness.
Khan AO. Ophthalmology. 2014 Mar; 121(3):e15. Epub 2013 Dec 12.

RefSeq genomic sequence
See the genomic reference sequence for the CABP4 gene (NG_021211.1).
RefSeq protein isoforms
See 7 reference sequence protein isoforms for the CABP4 gene.

PubMed
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Protein (RefSeq)
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Related structures

P57796 [Domain Mapping of Disease Mut...]
P57796
Domain Mapping of Disease Mutations
MODBASE, Database of Comparative Protein Structure Models (Sali Lab/UCSF) [MODBASE, Database of Comparat...]
MODBASE, Database of Comparative Protein Structure Models (Sali Lab/UCSF)
Transcript/Protein Information [PANTHER Classification System]
Transcript/Protein Information
PANTHER Classification System
reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome

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Protein