RHOXF1

Rhox homeobox family, member 1

Identifiers

RHOXF1; MGC119030; MGC119033; OTEX; PEPP1

External IDs

OMIM: 300446 MGI: 1920864 HomoloGene: 64643 GeneCards: RHOXF1 Gene

Gene Ontology
Molecular function	• DNA binding • sequence-specific DNA binding transcription factor activity • sequence-specific DNA binding
Cellular component	• nucleus
Biological process	• transcription, DNA-dependent • regulation of transcription, DNA-dependent • multicellular organismal development • gamete generation • sexual reproduction • steroid hormone receptor signaling pathway
Sources: Amigo / QuickGO

RNA expression pattern

More reference expression data

Orthologs

Species

Human

Mouse

ENSG00000101883

ENSMUSG00000050197

RefSeq (mRNA)

RefSeq (protein)

Location (UCSC)

Chr X:
119.24 – 119.25 Mb

Chr X:
34.37 – 34.37 Mb

PubMed search

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

References

^ 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. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=1222745.
^ 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". http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=158800.

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. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=2665286.
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. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=528928.
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. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=442147.
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. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=139241.