RHOXF1

RHOXF1
Identifiers
Aliases	RHOXF1, OTEX, PEPP1, Rhox homeobox family member 1
External IDs	HomoloGene: 64643 GeneCards: RHOXF1
Gene ontology Molecular function • transcription factor activity, sequence-specific DNA binding • DNA binding • sequence-specific DNA binding Cellular component • nucleus Biological process • multicellular organism development • gamete generation • regulation of transcription, DNA-templated • intracellular steroid hormone receptor signaling pathway • sexual reproduction • transcription, DNA-templated Sources:Amigo / QuickGO
RNA expression pattern
More reference expression data
Orthologs
Species	Human	Mouse
Entrez	158800	n/a
Ensembl	ENSG00000101883	n/a
UniProt	Q8NHV9	n/a
RefSeq (mRNA)	NM_139282	n/a
RefSeq (protein)	NP_644811.1	n/a
Location (UCSC)	Chr X: 120.11 – 120.12 Mb	n/a
PubMed search	[1]	n/a
Wikidata

View/Edit Human

Rhox homeobox family member 1 is a protein that in humans is encoded by the RHOXF1 gene.^[2][3][4]

References

1. "Human PubMed Reference:".
2. 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.
3. 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.
4. "Entrez Gene: OTEX paired-like homeobox protein OTEX".

Further reading

• 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.