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Gene Review

RP25  -  retinitis pigmentosa 25 (autosomal recessive)

Homo sapiens

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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


  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]
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