RecName: Full=Cadherin-related family member 1; AltName: Full=MT-proto - Protein

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Identification of a novel mutation in the CDHR1 gene in a family with recessive retinal degeneration. [Arch Ophthalmol. 2012]
Identification of a novel mutation in the CDHR1 gene in a family with recessive retinal degeneration.
Duncan JL, Roorda A, Navani M, Vishweswaraiah S, Syed R, Soudry S, Ratnam K, Gudiseva HV, Lee P, Gaasterland T, et al. Arch Ophthalmol. 2012 Oct; 130(10):1301-8.
Mutations in PCDH21 cause autosomal recessive cone-rod dystrophy. [J Med Genet. 2010]
Mutations in PCDH21 cause autosomal recessive cone-rod dystrophy.
Ostergaard E, Batbayli M, Duno M, Vilhelmsen K, Rosenberg T. J Med Genet. 2010 Oct; 47(10):665-9. Epub 2010 Aug 30.
A photoreceptor-specific cadherin is essential for the structural integrity of the outer segment and for photoreceptor survival. [Neuron. 2001]
A photoreceptor-specific cadherin is essential for the structural integrity of the outer segment and for photoreceptor survival.
Rattner A, Smallwood PM, Williams J, Cooke C, Savchenko A, Lyubarsky A, Pugh EN, Nathans J. Neuron. 2001 Dec 6; 32(5):775-86.

RefSeq protein
See the reference protein sequence for cadherin-related family member 1 precursor (NP_446024.1).

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Transcript/Protein Information [PANTHER Classification System]
Transcript/Protein Information
PANTHER Classification System
reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome

RecName: Full=Cadherin-related family member 1; AltName: Full=MT-protocadherin; ...
RecName: Full=Cadherin-related family member 1; AltName: Full=MT-protocadherin; AltName: Full=Photoreceptor cadherin; Short=prCAD; AltName: Full=Protocadherin-21; Flags: Precursor
gi|81871530|sp|Q91XU7.1|CDHR1_RAT

Protein
LOC129931980 [Homo sapiens]
LOC129931980 [Homo sapiens]
Gene ID:129931980

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Protein