PORCN
porcupine homolog (Drosophila) | |
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Identifiers | |
Symbol | PORCN |
Entrez | 64840 |
HUGO | 17652 |
OMIM | 300651 |
RefSeq | NM_022825 |
UniProt | Q9H237 |
Other data | |
Locus | Chr. X p11.23 |
WikiDoc Resources for PORCN |
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Media |
Evidence Based Medicine |
Clinical Trials |
Ongoing Trials on PORCN at Clinical Trials.gov Clinical Trials on PORCN at Google
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Guidelines / Policies / Govt |
US National Guidelines Clearinghouse on PORCN
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Books |
News |
Commentary |
Definitions |
Patient Resources / Community |
Directions to Hospitals Treating PORCN Risk calculators and risk factors for PORCN
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Healthcare Provider Resources |
Continuing Medical Education (CME) |
International |
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Business |
Experimental / Informatics |
PORCN (porcupine homolog – Drosophila) is a human gene.[1][2]
Function
The protein encoded by this gene an endoplasmic reticulum transmembrane protein involved in processing of wingless proteins such as WNT7A.[2]
Disease linkage
Mutations in this gene are associated with focal dermal hypoplasia.[3]
References
- ↑ Tanaka K, Okabayashi K, Asashima M, Perrimon N, Kadowaki T (2000). "The evolutionarily conserved porcupine gene family is involved in the processing of the Wnt family". Eur. J. Biochem. 267 (13): 4300–11. doi:10.1046/j.1432-1033.2000.01478.x. PMID 10866835. Unknown parameter
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ignored (help) - ↑ 2.0 2.1 Caricasole A, Ferraro T, Rimland JM, Terstappen GC (2002). "Molecular cloning and initial characterization of the MG61/PORC gene, the human homologue of the Drosophila segment polarity gene Porcupine". Gene. 288 (1–2): 147–57. doi:10.1016/S0378-1119(02)00467-5. PMID 12034504. Unknown parameter
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ignored (help) - ↑ Wang X, Reid Sutton V, Omar Peraza-Llanes J; et al. (2007). "Mutations in X-linked PORCN, a putative regulator of Wnt signaling, cause focal dermal hypoplasia". Nat. Genet. 39 (7): 836–8. doi:10.1038/ng2057. PMID 17546030. Unknown parameter
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ignored (help)