FBXW10: Difference between revisions

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'''F-box/WD repeat-containing protein 10''' is a [[protein]] that in humans is encoded by the ''FBXW10'' [[gene]].<ref name="pmid9787083">{{cite journal | vauthors = Kennerson ML, Nassif NT, Nicholson GA | title = Genomic structure and physical mapping of C17orf1: a gene associated with the proximal element of the CMT1A-REP binary repeat | journal = Genomics | volume = 53 | issue = 1 | pages = 110–2 |date=Dec 1998 | pmid = 9787083 | pmc =  | doi = 10.1006/geno.1998.5453 }}</ref><ref name="pmid7586531">{{cite journal | vauthors = Kennerson ML, Gordon MJ, Blair IP, Nicholson GA | title = Single test for two hereditary neuropathies, CMT1A and HNPP | journal = Clin Chem | volume = 41 | issue = 10 | pages = 1534–5 |date=Dec 1995 | pmid = 7586531 | pmc =  | doi =  }}</ref><ref name="entrez">{{cite web | title = Entrez Gene: FBXW10 F-box and WD repeat domain containing 10| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=10517| accessdate = }}</ref>
'''F-box/WD repeat-containing protein 10''' is a [[protein]] that in humans is encoded by the ''FBXW10'' [[gene]].<ref name="pmid9787083">{{cite journal | vauthors = Kennerson ML, Nassif NT, Nicholson GA | title = Genomic structure and physical mapping of C17orf1: a gene associated with the proximal element of the CMT1A-REP binary repeat | journal = Genomics | volume = 53 | issue = 1 | pages = 110–2 |date=Dec 1998 | pmid = 9787083 | pmc =  | doi = 10.1006/geno.1998.5453 }}</ref><ref name="pmid7586531">{{cite journal | vauthors = Kennerson ML, Gordon MJ, Blair IP, Nicholson GA | title = Single test for two hereditary neuropathies, CMT1A and HNPP | journal = Clin Chem | volume = 41 | issue = 10 | pages = 1534–5 |date=Dec 1995 | pmid = 7586531 | pmc =  | doi =  }}</ref><ref name="entrez">{{cite web | title = Entrez Gene: FBXW10 F-box and WD repeat domain containing 10| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=10517| accessdate = }}</ref>
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{{PBB_Summary
{{PBB_Summary
| section_title =  
| section_title =  
| summary_text = Members of the F-box protein family, such as FBXW10, are characterized by an approximately 40-amino acid F-box motif. SCF complexes, formed by SKP1 (MIM 601434), cullin (see CUL1; MIM 603034), and F-box proteins, act as protein-ubiquitin ligases. F-box proteins interact with SKP1 through the F box, and they interact with ubiquitination targets through other protein interaction domains (Jin et al., 2004).[supplied by OMIM]<ref name="entrez" />
| summary_text = Members of the [[F-box]] protein family, such as FBXW10, are characterized by an approximately 40-amino acid F-box motif. SCF complexes, formed by [[SKP1]] (MIM 601434), [[cullin]] (see [[CUL1]]; MIM 603034), and F-box proteins, act as protein-ubiquitin [[ligases]]. F-box proteins interact with SKP1 through the F box, and they interact with ubiquitination targets through other protein interaction domains (Jin et al., 2004).[supplied by OMIM]<ref name="entrez" />
}}
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Latest revision as of 16:41, 14 February 2018

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Identifiers
Aliases
External IDsGeneCards: [1]
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

n/a

n/a

RefSeq (protein)

n/a

n/a

Location (UCSC)n/an/a
PubMed searchn/an/a
Wikidata
View/Edit Human

F-box/WD repeat-containing protein 10 is a protein that in humans is encoded by the FBXW10 gene.[1][2][3]

Members of the F-box protein family, such as FBXW10, are characterized by an approximately 40-amino acid F-box motif. SCF complexes, formed by SKP1 (MIM 601434), cullin (see CUL1; MIM 603034), and F-box proteins, act as protein-ubiquitin ligases. F-box proteins interact with SKP1 through the F box, and they interact with ubiquitination targets through other protein interaction domains (Jin et al., 2004).[supplied by OMIM][3]

References

  1. Kennerson ML, Nassif NT, Nicholson GA (Dec 1998). "Genomic structure and physical mapping of C17orf1: a gene associated with the proximal element of the CMT1A-REP binary repeat". Genomics. 53 (1): 110–2. doi:10.1006/geno.1998.5453. PMID 9787083.
  2. Kennerson ML, Gordon MJ, Blair IP, Nicholson GA (Dec 1995). "Single test for two hereditary neuropathies, CMT1A and HNPP". Clin Chem. 41 (10): 1534–5. PMID 7586531.
  3. 3.0 3.1 "Entrez Gene: FBXW10 F-box and WD repeat domain containing 10".

Further reading