POF1B

POF1B
Available structures
PDB	Ortholog search: PDBe RCSB
List of PDB id codes
	3BH9
Identifiers
Aliases	POF1B, POF, POF2B, premature ovarian failure, 1B, actin binding protein, POF1B actin binding protein
External IDs	OMIM: 300603 MGI: 1916943 HomoloGene: 11785 GeneCards: POF1B
Gene location (Human)
Chr.	X chromosome (human)[1]
End	85,379,717 bp[1]
Gene location (Mouse)
Chr.	X chromosome (mouse)[2]
End	112,698,651 bp[2]
RNA expression pattern
	More reference expression data
Gene ontology
Molecular function	• actin binding; • actin filament binding;
Cellular component	• desmosome; • cell junction; • actin filament; • adherens junction; • bicellular tight junction;
Biological process	• epithelial cell morphogenesis; • actin filament organization; • actin cytoskeleton organization; • bicellular tight junction assembly;
	Sources:Amigo / QuickGO
Orthologs
	79983
	69693
	ENSG00000124429
	ENSMUSG00000034607
	Q8WVV4
	Q8K4L4
	NM_001307940; NM_024921
	NM_181579
	NP_001294869; NP_079197
	NP_853557
	Wikidata
View/Edit Human	View/Edit Mouse

Protein POF1B is a protein that in humans is encoded by the POF1B gene.[5][6]

References

GRCh38: Ensembl release 89: ENSG00000124429 - Ensembl, May 2017
GRCm38: Ensembl release 89: ENSMUSG00000034607 - 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.
Bione S, Toniolo D (Apr 2001). "X chromosome genes and premature ovarian failure". Semin Reprod Med. 18 (1): 51–7. doi:10.1055/s-2000-13475. PMID 11299520.
"Entrez Gene: POF1B premature ovarian failure, 1B".

Maruyama K, Sugano S (1994). "Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides". Gene. 138 (1–2): 171–4. doi:10.1016/0378-1119(94)90802-8. PMID 8125298.
Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, et al. (1997). "Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library". Gene. 200 (1–2): 149–56. doi:10.1016/S0378-1119(97)00411-3. PMID 9373149.
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.
Bione S, Rizzolio F, Sala C, et al. (2005). "Mutation analysis of two candidate genes for premature ovarian failure, DACH2 and POF1B". Hum. Reprod. 19 (12): 2759–66. doi:10.1093/humrep/deh502. PMID 15459172.
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.
Ross MT, Grafham DV, Coffey AJ, et al. (2005). "The DNA sequence of the human X chromosome". Nature. 434 (7031): 325–37. doi:10.1038/nature03440. PMC 2665286. PMID 15772651.
Lacombe A, Lee H, Zahed L, et al. (2006). "Disruption of POF1B Binding to Nonmuscle Actin Filaments Is Associated with Premature Ovarian Failure". Am. J. Hum. Genet. 79 (1): 113–9. doi:10.1086/505406. PMC 1474115. PMID 16773570.

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[refGRCh38Ensembl-1] GRCh38: Ensembl release 89: ENSG00000124429 - Ensembl, May 2017

[refGRCm38Ensembl-2] GRCm38: Ensembl release 89: ENSMUSG00000034607 - Ensembl, May 2017

[3] "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[4] "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[pmid11299520-5] Bione S, Toniolo D (Apr 2001). "X chromosome genes and premature ovarian failure". Semin Reprod Med. 18 (1): 51–7. doi:10.1055/s-2000-13475. PMID 11299520.

[entrez-6] "Entrez Gene: POF1B premature ovarian failure, 1B".

POF1B

References

Further reading