RHOXF1

RHOXF1
Identifiers
Aliases	RHOXF1, OTEX, PEPP1, Rhox homeobox family member 1
External IDs	OMIM: 300446 HomoloGene: 64643 GeneCards: RHOXF1
Gene location (Human)
Chr.	X chromosome (human)[1]
End	120,115,913 bp[1]
RNA expression pattern
	More reference expression data
Gene ontology
Molecular function	• GO:0001131, GO:0001151, GO:0001130, GO:0001204 DNA-binding transcription factor activity; • DNA binding; • sequence-specific DNA binding; • GO:0001200, GO:0001133, GO:0001201 DNA-binding transcription factor activity, RNA polymerase II-specific; • RNA polymerase II regulatory region sequence-specific DNA binding;
Cellular component	• cell nucleus;
Biological process	• multicellular organism development; • gamete generation; • regulation of transcription, DNA-templated; • intracellular steroid hormone receptor signaling pathway; • sexual reproduction; • transcription, DNA-templated; • positive regulation of gene expression; • regulation of transcription from RNA polymerase II promoter;
	Sources:Amigo / QuickGO
Orthologs
	158800
	n/a
	ENSG00000101883
	n/a
	Q8NHV9
	n/a
	NM_139282
	n/a
	NP_644811
	n/a
	Wikidata
View/Edit Human

Rhox homeobox family member 1 is a protein that in humans is encoded by the RHOXF1 gene.[3][4][5]

References

GRCh38: Ensembl release 89: ENSG00000101883 - Ensembl, May 2017
"Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
Geserick C, Weiss B, Schleuning WD, Haendler B (Aug 2002). "OTEX, an androgen-regulated human member of the paired-like class of homeobox genes". Biochem J. 366 (Pt 1): 367–75. doi:10.1042/BJ20020399. PMC 1222745. PMID 11980563.
Wayne CM, MacLean JA, Cornwall G, Wilkinson MF (Dec 2002). "Two novel human X-linked homeobox genes, hPEPP1 and hPEPP2, selectively expressed in the testis". Gene. 301 (1–2): 1–11. doi:10.1016/S0378-1119(02)01087-9. PMID 12490318.
"Entrez Gene: OTEX paired-like homeobox protein OTEX".

Lim J, Hao T, Shaw C, et al. (2006). "A protein-protein interaction network for human inherited ataxias and disorders of Purkinje cell degeneration". Cell. 125 (4): 801–14. doi:10.1016/j.cell.2006.03.032. PMID 16713569.
Rual JF, Venkatesan K, Hao T, et al. (2005). "Towards a proteome-scale map of the human protein-protein interaction network". Nature. 437 (7062): 1173–8. doi:10.1038/nature04209. PMID 16189514.
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.
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.
Lehner B, Sanderson CM (2004). "A protein interaction framework for human mRNA degradation". Genome Res. 14 (7): 1315–23. doi:10.1101/gr.2122004. PMC 442147. PMID 15231747.
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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