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'''Cytokine receptor-like factor 1''' is a [[protein]] that in humans is encoded by the ''CRLF1'' [[gene]].<ref name="pmid9686600">{{cite journal | vauthors = Elson GC, Graber P, Losberger C, Herren S, Gretener D, Menoud LN, Wells TN, Kosco-Vilbois MH, Gauchat JF | title = Cytokine-like factor-1, a novel soluble protein, shares homology with members of the cytokine type I receptor family | journal = J Immunol | volume = 161 | issue = 3 | pages = 1371–9 |date=Aug 1998 | pmid = 9686600 | pmc = | doi = }}</ref><ref name="entrez">{{cite web | title = Entrez Gene: CRLF1 cytokine receptor-like factor 1| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=9244| accessdate = }}</ref> | |||
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'''Cytokine receptor-like factor 1''' is a [[protein]] that in humans is encoded by the ''CRLF1'' [[gene]].<ref name="pmid9686600">{{cite journal | | |||
== Function == | == Function == | ||
| Line 13: | Line 9: | ||
Mutations in this gene are associated with two conditions, both [[rare disease|rare]]: | Mutations in this gene are associated with two conditions, both [[rare disease|rare]]: | ||
*''Cold-induced sweating syndrome'', characterized by profuse [[hyperhidrosis]] in cold environmental temperature and characteristic craniofacial and skeletal features)<ref name=Yamazaki2010>{{cite journal | | *''Cold-induced sweating syndrome'', characterized by profuse [[hyperhidrosis]] in cold environmental temperature and characteristic craniofacial and skeletal features)<ref name=Yamazaki2010>{{cite journal | vauthors = Yamazaki M, Kosho T, Kawachi S, Mikoshiba M, Takahashi J, Sano R, Oka K, Yoshida K, Watanabe T, Kato H, Komatsu M, Kawamura R, Wakui K, Knappskog PM, Boman H, Fukushima Y | title = Cold-induced sweating syndrome with neonatal features of Crisponi syndrome: longitudinal observation of a patient homozygous for a CRLF1 mutation | journal = Am. J. Med. Genet. A | volume = 152A | issue = 3 | pages = 764–9 |date=March 2010 | pmid = 20186812 | doi = 10.1002/ajmg.a.33315 | url = | issn = }}</ref><ref name="pmid16782820">{{cite journal | vauthors = Rousseau F, Gauchat JF, McLeod JG, Chevalier S, Guillet C, Guilhot F, Cognet I, Froger J, Hahn AF, Knappskog PM, Gascan H, Boman H | title = Inactivation of cardiotrophin-like cytokine, a second ligand for ciliary neurotrophic factor receptor, leads to cold-induced sweating syndrome in a patient | journal = Proc. Natl. Acad. Sci. U.S.A. | volume = 103 | issue = 26 | pages = 10068–73 |date=June 2006 | pmid = 16782820 | pmc = 1502507 | doi = 10.1073/pnas.0509598103 | url = | issn = }}</ref> | ||
*''Crisponi syndrome'' (CS), characterized by neonatal-onset paroxysmal muscular contractions, abnormal function of the [[autonomic nervous system]] and craniofacial and skeletal manifestations such as thick and arched eyebrows, a short nose with anteverted nostrils, full cheeks, an inverted upper lip and a small mouth.<ref name=Yamazaki2010/> | *''Crisponi syndrome'' (CS), characterized by neonatal-onset paroxysmal muscular contractions, abnormal function of the [[autonomic nervous system]] and craniofacial and skeletal manifestations such as thick and arched eyebrows, a short nose with anteverted nostrils, full cheeks, an inverted upper lip and a small mouth.<ref name=Yamazaki2010/> | ||
It is unknown whether the two conditions are distinct clinical entities or a single clinical entity with variable expressions.<ref name=Yamazaki2010/> | It is unknown whether the two conditions are distinct clinical entities or a single clinical entity with variable expressions.<ref name=Yamazaki2010/> | ||
Other characteristic features in CRLF1 mutation include [[marfanoid habitus]] with progressive kyphoscoliosis and craniofacial characteristics including [[dolichocephaly]], a slender face with poor expression, a nose with hypoplastic nares, [[malar hypoplasia]] and [[prognathism]].<ref name=Yamazaki2010/> | Other characteristic features in CRLF1 mutation include [[marfanoid habitus]] with progressive kyphoscoliosis and craniofacial characteristics including [[dolichocephaly]], a slender face with poor expression, a nose with hypoplastic nares, [[malar hypoplasia]] and [[prognathism]].<ref name=Yamazaki2010/> | ||
== References == | == References == | ||
| Line 23: | Line 19: | ||
== Further reading == | == Further reading == | ||
{{refbegin | 2}} | {{refbegin | 2}} | ||
*{{cite journal | | *{{cite journal | vauthors=Elson GC, Lelièvre E, Guillet C |title=CLF associates with CLC to form a functional heteromeric ligand for the CNTF receptor complex. |journal=Nat. Neurosci. |volume=3 |issue= 9 |pages= 867–72 |year= 2000 |pmid= 10966616 |doi= 10.1038/78765 |display-authors=etal}} | ||
*{{cite journal | | *{{cite journal | vauthors=Lelièvre E, Plun-Favreau H, Chevalier S |title=Signaling pathways recruited by the cardiotrophin-like cytokine/cytokine-like factor-1 composite cytokine: specific requirement of the membrane-bound form of ciliary neurotrophic factor receptor alpha component. |journal=J. Biol. Chem. |volume=276 |issue= 25 |pages= 22476–84 |year= 2001 |pmid= 11294841 |doi= 10.1074/jbc.M101681200 |display-authors=etal}} | ||
*{{cite journal | | *{{cite journal | vauthors=Strausberg RL, Feingold EA, Grouse LH |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899 | pmc=139241 |display-authors=etal}} | ||
*{{cite journal | | *{{cite journal | vauthors=Knappskog PM, Majewski J, Livneh A |title=Cold-induced sweating syndrome is caused by mutations in the CRLF1 gene. |journal=Am. J. Hum. Genet. |volume=72 |issue= 2 |pages= 375–83 |year= 2003 |pmid= 12509788 |doi=10.1086/346120 | pmc=379230 |display-authors=etal}} | ||
*{{cite journal | | *{{cite journal | vauthors=Clark HF, Gurney AL, Abaya E |title=The secreted protein discovery initiative (SPDI), a large-scale effort to identify novel human secreted and transmembrane proteins: a bioinformatics assessment. |journal=Genome Res. |volume=13 |issue= 10 |pages= 2265–70 |year= 2003 |pmid= 12975309 |doi= 10.1101/gr.1293003 | pmc=403697 |display-authors=etal}} | ||
*{{cite journal | | *{{cite journal | vauthors=Heese K, Yamada T, Akatsu H |title=Characterizing the new transcription regulator protein p60TRP. |journal=J. Cell. Biochem. |volume=91 |issue= 5 |pages= 1030–42 |year= 2005 |pmid= 15034937 |doi= 10.1002/jcb.20010 |display-authors=etal}} | ||
*{{cite journal | | *{{cite journal | vauthors=Zhang Z, Henzel WJ |title=Signal peptide prediction based on analysis of experimentally verified cleavage sites. |journal=Protein Sci. |volume=13 |issue= 10 |pages= 2819–24 |year= 2005 |pmid= 15340161 |doi= 10.1110/ps.04682504 | pmc=2286551 }} | ||
*{{cite journal | | *{{cite journal | vauthors=Gerhard DS, Wagner L, Feingold EA |title=The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). |journal=Genome Res. |volume=14 |issue= 10B |pages= 2121–7 |year= 2004 |pmid= 15489334 |doi= 10.1101/gr.2596504 | pmc=528928 |display-authors=etal}} | ||
*{{cite journal | | *{{cite journal | vauthors=Dagoneau N, Bellais S, Blanchet P |title=Mutations in cytokine receptor-like factor 1 (CRLF1) account for both Crisponi and cold-induced sweating syndromes. |journal=Am. J. Hum. Genet. |volume=80 |issue= 5 |pages= 966–70 |year= 2007 |pmid= 17436251 |doi= 10.1086/513608 | pmc=1852726 |display-authors=etal}} | ||
*{{cite journal | | *{{cite journal | vauthors=Crisponi L, Crisponi G, Meloni A |title=Crisponi syndrome is caused by mutations in the CRLF1 gene and is allelic to cold-induced sweating syndrome type 1. |journal=Am. J. Hum. Genet. |volume=80 |issue= 5 |pages= 971–81 |year= 2007 |pmid= 17436252 |doi= 10.1086/516843 | pmc=1852730 |display-authors=etal}} | ||
{{refend}} | {{refend}} | ||
==External links== | ==External links== | ||
* [ | * [https://www.ncbi.nlm.nih.gov/books/NBK52917/ GeneReviews/NCBI/NIH/UW entry on Cold-Induced Sweating Syndrome including Crisponi Syndrome] | ||
* [ | * [https://www.ncbi.nlm.nih.gov/omim/601559,193700,601680,272430,601378,604237,607672,610313,272430,601378,604237,607672,610313 OMIM enries on Cold-Induced Sweating Syndrome including Crisponi Syndrome] | ||
* {{UCSC gene info|CRLF1}} | |||
{{NLM content}} | {{NLM content}} | ||
{{Cytokine receptor modulators}} | |||
{{gene-19-stub}} | {{gene-19-stub}} | ||
Latest revision as of 10:03, 30 August 2017
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Cytokine receptor-like factor 1 is a protein that in humans is encoded by the CRLF1 gene.[1][2]
Function
This gene encodes a member of the cytokine type I receptor family. The protein forms a secreted complex with cardiotrophin-like cytokine factor 1 and acts on cells expressing ciliary neurotrophic factor receptors. The complex can promote survival of neuronal cells.[2]
Clinical significance
Mutations in this gene are associated with two conditions, both rare:
- Cold-induced sweating syndrome, characterized by profuse hyperhidrosis in cold environmental temperature and characteristic craniofacial and skeletal features)[3][4]
- Crisponi syndrome (CS), characterized by neonatal-onset paroxysmal muscular contractions, abnormal function of the autonomic nervous system and craniofacial and skeletal manifestations such as thick and arched eyebrows, a short nose with anteverted nostrils, full cheeks, an inverted upper lip and a small mouth.[3]
It is unknown whether the two conditions are distinct clinical entities or a single clinical entity with variable expressions.[3] Other characteristic features in CRLF1 mutation include marfanoid habitus with progressive kyphoscoliosis and craniofacial characteristics including dolichocephaly, a slender face with poor expression, a nose with hypoplastic nares, malar hypoplasia and prognathism.[3]
References
- ↑ Elson GC, Graber P, Losberger C, Herren S, Gretener D, Menoud LN, Wells TN, Kosco-Vilbois MH, Gauchat JF (Aug 1998). "Cytokine-like factor-1, a novel soluble protein, shares homology with members of the cytokine type I receptor family". J Immunol. 161 (3): 1371–9. PMID 9686600.
- ↑ 2.0 2.1 "Entrez Gene: CRLF1 cytokine receptor-like factor 1".
- ↑ 3.0 3.1 3.2 3.3 Yamazaki M, Kosho T, Kawachi S, Mikoshiba M, Takahashi J, Sano R, Oka K, Yoshida K, Watanabe T, Kato H, Komatsu M, Kawamura R, Wakui K, Knappskog PM, Boman H, Fukushima Y (March 2010). "Cold-induced sweating syndrome with neonatal features of Crisponi syndrome: longitudinal observation of a patient homozygous for a CRLF1 mutation". Am. J. Med. Genet. A. 152A (3): 764–9. doi:10.1002/ajmg.a.33315. PMID 20186812.
- ↑ Rousseau F, Gauchat JF, McLeod JG, Chevalier S, Guillet C, Guilhot F, Cognet I, Froger J, Hahn AF, Knappskog PM, Gascan H, Boman H (June 2006). "Inactivation of cardiotrophin-like cytokine, a second ligand for ciliary neurotrophic factor receptor, leads to cold-induced sweating syndrome in a patient". Proc. Natl. Acad. Sci. U.S.A. 103 (26): 10068–73. doi:10.1073/pnas.0509598103. PMC 1502507. PMID 16782820.
Further reading
- Elson GC, Lelièvre E, Guillet C, et al. (2000). "CLF associates with CLC to form a functional heteromeric ligand for the CNTF receptor complex". Nat. Neurosci. 3 (9): 867–72. doi:10.1038/78765. PMID 10966616.
- Lelièvre E, Plun-Favreau H, Chevalier S, et al. (2001). "Signaling pathways recruited by the cardiotrophin-like cytokine/cytokine-like factor-1 composite cytokine: specific requirement of the membrane-bound form of ciliary neurotrophic factor receptor alpha component". J. Biol. Chem. 276 (25): 22476–84. doi:10.1074/jbc.M101681200. PMID 11294841.
- Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
- Knappskog PM, Majewski J, Livneh A, et al. (2003). "Cold-induced sweating syndrome is caused by mutations in the CRLF1 gene". Am. J. Hum. Genet. 72 (2): 375–83. doi:10.1086/346120. PMC 379230. PMID 12509788.
- Clark HF, Gurney AL, Abaya E, et al. (2003). "The secreted protein discovery initiative (SPDI), a large-scale effort to identify novel human secreted and transmembrane proteins: a bioinformatics assessment". Genome Res. 13 (10): 2265–70. doi:10.1101/gr.1293003. PMC 403697. PMID 12975309.
- Heese K, Yamada T, Akatsu H, et al. (2005). "Characterizing the new transcription regulator protein p60TRP". J. Cell. Biochem. 91 (5): 1030–42. doi:10.1002/jcb.20010. PMID 15034937.
- Zhang Z, Henzel WJ (2005). "Signal peptide prediction based on analysis of experimentally verified cleavage sites". Protein Sci. 13 (10): 2819–24. doi:10.1110/ps.04682504. PMC 2286551. PMID 15340161.
- Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMC 528928. PMID 15489334.
- Dagoneau N, Bellais S, Blanchet P, et al. (2007). "Mutations in cytokine receptor-like factor 1 (CRLF1) account for both Crisponi and cold-induced sweating syndromes". Am. J. Hum. Genet. 80 (5): 966–70. doi:10.1086/513608. PMC 1852726. PMID 17436251.
- Crisponi L, Crisponi G, Meloni A, et al. (2007). "Crisponi syndrome is caused by mutations in the CRLF1 gene and is allelic to cold-induced sweating syndrome type 1". Am. J. Hum. Genet. 80 (5): 971–81. doi:10.1086/516843. PMC 1852730. PMID 17436252.
External links
- GeneReviews/NCBI/NIH/UW entry on Cold-Induced Sweating Syndrome including Crisponi Syndrome
- OMIM enries on Cold-Induced Sweating Syndrome including Crisponi Syndrome
- Human CRLF1 genome location and CRLF1 gene details page in the UCSC Genome Browser.
This article incorporates text from the United States National Library of Medicine, which is in the public domain.
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