NPC1
| enfermedad de Niemann-Pick, tipo C1 | ||||
|---|---|---|---|---|
| Estructuras disponibles | ||||
| PDB | Buscar ortólogos: PDBe, RCSB | |||
| Identificadores | ||||
| Símbolo | NPC1 (HGNC: 7897) | |||
| Identificadores externos |
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| Locus | Cr. 18 q11-q12 | |||
| Patrón de expresión de ARNm | ||||
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| Más información | ||||
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| Entrez |
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| Ensembl |
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| UniProt |
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| RefSeq (ARNm) |
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| RefSeq (proteína) NCBI |
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| Ubicación (UCSC) |
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| PubMed (Búsqueda) |
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NPC1 es el nombre de una proteína codificada por el gen homónimo, Npc1, que se encuentra localizado en el brazo largo del cromosoma 18 en humanos. El gen codifica para una proteína de membrana de paso sencillo, de 1.278 aminoácidos, que tras la traducción es insertada en la membrana de los lisosomas y los endosomas tardíos. Mutaciones en este gen se relacionan con la enfermedad de Niemann-Pick.[1][2][3]
Referencias
- ↑ «Entrez Gene: NPC1 Niemann-Pick disease, type C1». Consultado el 6 de mayo de 2014.
- ↑ Carstea ED, Polymeropoulos MH, Parker CC, Detera-Wadleigh SD, O'Neill RR, Patterson MC, Goldin E, Xiao H, Straub RE, Vanier MT (marzo de 1993). «Linkage of Niemann-Pick disease type C to human chromosome 18». Proc. Natl. Acad. Sci. U.S.A. 90 (5): 2002-4. PMC 46008. PMID 8446622. doi:10.1073/pnas.90.5.2002.
- ↑ Carstea ED, Morris JA, Coleman KG, Loftus SK, Zhang D, Cummings C, Gu J, Rosenfeld MA, Pavan WJ, Krizman DB, Nagle J, Polymeropoulos MH, Sturley SL, Ioannou YA, Higgins ME, Comly M, Cooney A, Brown A, Kaneski CR, Blanchette-Mackie EJ, Dwyer NK, Neufeld EB, Chang TY, Liscum L, Strauss JF 3rd, Ohno K, Zeigler M, Carmi R, Sokol J, Markie D, O'Neill RR, van Diggelen OP, Elleder M, Patterson MC, Brady RO, Vanier MT, Pentchev PG, Tagle DA (julio de 1997). «Niemann-Pick C1 disease gene: homology to mediators of cholesterol homeostasis». Science 277 (5323): 228-31. PMID 9211849. doi:10.1126/science.277.5323.228.
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