The world's first wiki where authorship really matters (Nature Genetics, 2008). Due credit and reputation for authors. Imagine a global collaborative knowledge base for original thoughts. Search thousands of articles and collaborate with scientists around the globe.

wikigene or wiki gene protein drug chemical gene disease author authorship tracking collaborative publishing evolutionary knowledge reputation system wiki2.0 global collaboration genes proteins drugs chemicals diseases compound
Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 
Gene Review

RP25  -  retinitis pigmentosa 25 (autosomal recessive)

Homo sapiens

This record was replaced with 346007.
 
 
Welcome! If you are familiar with the subject of this article, you can contribute to this open access knowledge base by deleting incorrect information, restructuring or completely rewriting any text. Read more.
 

Disease relevance of RP25

  • PURPOSE: To identify the disease gene in five Spanish families with autosomal recessive retinitis pigmentosa (arRP) linked to the RP25 locus [1].
 

High impact information on RP25

 

Associations of RP25 with chemical compounds

  • RIM1, encoding a presynaptic protein involved in the glutamate neurotransmission, is the responsible gene for autosomal dominant cone-rod dystrophy CORD7, whose locus overlaps partially with a locus of autosomal recessive RP (arRP), RP25 [5].
 

Other interactions of RP25

References

  1. Molecular genetic analysis of two functional candidate genes in the autosomal recessive retinitis pigmentosa, RP25, locus. Abd El-Aziz, M.M., El-Ashry, M.F., Barragan, I., Marcos, I., Borrego, S., Antiñolo, G., Bhattacharya, S.S. Curr. Eye Res. (2005) [Pubmed]
  2. Refinement of the locus for autosomal recessive Retinitis pigmentosa (RP25) linked to chromosome 6q in a family of Pakistani origin. Khaliq, S., Hameed, A., Ismail, M., Mehdi, S.Q., Bessant, D.A., Payne, A.M., Bhattacharya, S.S. Am. J. Hum. Genet. (1999) [Pubmed]
  3. Mutation screening of three candidate genes, ELOVL5, SMAP1 and GLULD1 in autosomal recessive retinitis pigmentosa. Barragan, I., Marcos, I., Borrego, S., Antiñolo, G. Int. J. Mol. Med. (2005) [Pubmed]
  4. Molecular cloning and characterization of human RAB23, a member of the group of Rab GTPases. Marcos, I., Borrego, S., Antiñolo, G. Int. J. Mol. Med. (2003) [Pubmed]
  5. Molecular analysis of RIM1 in autosomal recessive Retinitis pigmentosa. Barragan, I., Marcos, I., Borrego, S., Antiñolo, G. Ophthalmic Res. (2005) [Pubmed]
  6. Evaluation of the ELOVL4 gene in families with retinitis pigmentosa linked to the RP25 locus. Li, Y., Marcos, I., Borrego, S., Yu, Z., Zhang, K., Antiñolo, G. J. Med. Genet. (2001) [Pubmed]
 
WikiGenes - Universities