FCHSD1

FCHSD1
Identifiers
Aliases	FCHSD1, NWK2, FCH and double SH3 domains 1
External IDs	OMIM: 617555 MGI: 2441771 HomoloGene: 14127 GeneCards: FCHSD1
Gene location (Human)
Chr.	Chromosome 5 (human)[1]
End	141,651,418 bp[1]
Gene location (Mouse)
Chr.	Chromosome 18 (mouse)[2]
End	37,969,774 bp[2]
RNA expression pattern
	More reference expression data
Gene ontology
Molecular function	• lipid binding;
Cellular component	• neuromuscular junction; • recycling endosome; • cuticular plate; • cytoplasm; • cytoplasmic vesicle; • cell projection; • perikaryon;
Biological process	• neuromuscular synaptic transmission; • regulation of actin filament polymerization; • positive regulation of actin filament polymerization; • multi-organism membrane organization;
	Sources:Amigo / QuickGO
Orthologs
	89848
	319262
	ENSG00000197948
	ENSMUSG00000038524
	Q86WN1
	Q6PFY1
	NM_033449
	NM_175684
	NP_258260
	NP_783615
	Wikidata
View/Edit Human	View/Edit Mouse

FCH and double SH3 domains protein 1 is a protein that in humans is encoded by the FCHSD1 gene.[5][6][7]

References

GRCh38: Ensembl release 89: ENSG00000197948 - Ensembl, May 2017
GRCm38: Ensembl release 89: ENSMUSG00000038524 - Ensembl, May 2017
"Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
Hattori A, Okumura K, Nagase T, Kikuno R, Hirosawa M, Ohara O (Feb 2001). "Characterization of long cDNA clones from human adult spleen". DNA Res. 7 (6): 357–66. doi:10.1093/dnares/7.6.357. PMID 11214971.
Katoh M, Katoh M (Apr 2004). "Identification and characterization of human FCHSD1 and FCHSD2 genes in silico". Int J Mol Med. 13 (5): 749–54. doi:10.3892/ijmm.13.5.749. PMID 15067381.
"Entrez Gene: FCHSD1 FCH and double SH3 domains 1".

Hillier LW, Graves TA, Fulton RS, et al. (2005). "Generation and annotation of the DNA sequences of human chromosomes 2 and 4". Nature. 434 (7034): 724–31. doi:10.1038/nature03466. PMID 15815621.
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.
Coyle IP, Koh YH, Lee WC, et al. (2004). "Nervous wreck, an SH3 adaptor protein that interacts with Wsp, regulates synaptic growth in Drosophila". Neuron. 41 (4): 521–34. doi:10.1016/S0896-6273(04)00016-9. PMID 14980202. S2CID 797812.
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.
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.
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.

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