FGD4: Difference between revisions
Jump to navigation
Jump to search
m (Bot: HTTP→HTTPS) |
imported>Jmertel23 (removed "underlinked" tag) |
||
| Line 1: | Line 1: | ||
{{Infobox_gene}} | {{Infobox_gene}} | ||
'''FYVE, RhoGEF and PH domain-containing protein 4''' is a [[protein]] that in humans is encoded by the ''FGD4'' [[gene]].<ref name="pmid11527409">{{cite journal | vauthors = Ikeda W, Nakanishi H, Takekuni K, Itoh S, Takai Y | title = Identification of splicing variants of Frabin with partly different functions and tissue distribution | journal = Biochem Biophys Res Commun | volume = 286 | issue = 5 | pages = 1066–72 |date=Aug 2001 | pmid = 11527409 | pmc = | doi = 10.1006/bbrc.2001.5481 }}</ref><ref name="entrez">{{cite web | title = Entrez Gene: FGD4 FYVE, RhoGEF and PH domain containing 4| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=121512| accessdate = }}</ref> | '''FYVE, RhoGEF and PH domain-containing protein 4''' is a [[protein]] that in humans is encoded by the ''FGD4'' [[gene]].<ref name="pmid11527409">{{cite journal | vauthors = Ikeda W, Nakanishi H, Takekuni K, Itoh S, Takai Y | title = Identification of splicing variants of Frabin with partly different functions and tissue distribution | journal = Biochem Biophys Res Commun | volume = 286 | issue = 5 | pages = 1066–72 |date=Aug 2001 | pmid = 11527409 | pmc = | doi = 10.1006/bbrc.2001.5481 }}</ref><ref name="entrez">{{cite web | title = Entrez Gene: FGD4 FYVE, RhoGEF and PH domain containing 4| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=121512| accessdate = }}</ref> | ||
Latest revision as of 16:13, 3 May 2018
| VALUE_ERROR (nil) | |||||||
|---|---|---|---|---|---|---|---|
| Identifiers | |||||||
| Aliases | |||||||
| External IDs | GeneCards: [1] | ||||||
| Orthologs | |||||||
| Species | Human | Mouse | |||||
| Entrez |
|
| |||||
| Ensembl |
|
| |||||
| UniProt |
|
| |||||
| RefSeq (mRNA) |
|
| |||||
| RefSeq (protein) |
|
| |||||
| Location (UCSC) | n/a | n/a | |||||
| PubMed search | n/a | n/a | |||||
| Wikidata | |||||||
| |||||||
FYVE, RhoGEF and PH domain-containing protein 4 is a protein that in humans is encoded by the FGD4 gene.[1][2]
References
- ↑ Ikeda W, Nakanishi H, Takekuni K, Itoh S, Takai Y (Aug 2001). "Identification of splicing variants of Frabin with partly different functions and tissue distribution". Biochem Biophys Res Commun. 286 (5): 1066–72. doi:10.1006/bbrc.2001.5481. PMID 11527409.
- ↑ "Entrez Gene: FGD4 FYVE, RhoGEF and PH domain containing 4".
Further reading
- Obaishi H, Nakanishi H, Mandai K, et al. (1998). "Frabin, a novel FGD1-related actin filament-binding protein capable of changing cell shape and activating c-Jun N-terminal kinase". J. Biol. Chem. 273 (30): 18697–700. doi:10.1074/jbc.273.30.18697. PMID 9668039.
- Ikeda W, Nakanishi H, Tanaka Y, et al. (2001). "Cooperation of Cdc42 small G protein-activating and actin filament-binding activities of frabin in microspike formation". Oncogene. 20 (27): 3457–63. doi:10.1038/sj.onc.1204463. PMID 11429692.
- 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.
- Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. 36 (1): 40–5. doi:10.1038/ng1285. PMID 14702039.
- Chen XM, Splinter PL, Tietz PS, et al. (2004). "Phosphatidylinositol 3-kinase and frabin mediate Cryptosporidium parvum cellular invasion via activation of Cdc42". J. Biol. Chem. 279 (30): 31671–8. doi:10.1074/jbc.M401592200. PMID 15133042.
- De Sandre-Giovannoli A, Delague V, Hamadouche T, et al. (2006). "Homozygosity mapping of autosomal recessive demyelinating Charcot-Marie-Tooth neuropathy (CMT4H) to a novel locus on chromosome 12p11.21-q13.11". J. Med. Genet. 42 (3): 260–5. doi:10.1136/jmg.2004.024364. PMC 1736004. PMID 15744041.
- Delague V, Jacquier A, Hamadouche T, et al. (2007). "Mutations in FGD4 encoding the Rho GDP/GTP exchange factor FRABIN cause autosomal recessive Charcot-Marie-Tooth type 4H". Am. J. Hum. Genet. 81 (1): 1–16. doi:10.1086/518428. PMC 1950914. PMID 17564959.
- Stendel C, Roos A, Deconinck T, et al. (2007). "Peripheral nerve demyelination caused by a mutant Rho GTPase guanine nucleotide exchange factor, frabin/FGD4". Am. J. Hum. Genet. 81 (1): 158–64. doi:10.1086/518770. PMC 1950925. PMID 17564972.
External links
 | This article on a gene on human chromosome 12 is a stub. You can help Wikipedia by expanding it. |