FOXD4
From Wikipedia, the free encyclopedia
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Forkhead box D4
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| Identifiers | ||||||||||||||
| Symbol(s) | FOXD4; FKHL9; FOXD4A; FREAC5; MGC105106 | |||||||||||||
| External IDs | OMIM: 601092 | |||||||||||||
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| RNA expression pattern | ||||||||||||||
| Orthologs | ||||||||||||||
| Human | Mouse | |||||||||||||
| Entrez | 2298 | n/a | ||||||||||||
| Ensembl | ENSG00000184492 | n/a | ||||||||||||
| Uniprot | Q12950 | n/a | ||||||||||||
| Refseq | NM_207305 (mRNA) NP_997188 (protein) |
n/a (mRNA) n/a (protein) |
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| Location | Chr 9: 0.11 - 0.11 Mb | n/a | ||||||||||||
| Pubmed search | [1] | n/a | ||||||||||||
Forkhead box D4, also known as FOXD4, is a human gene.[1]
[edit] References
[edit] Further reading
- Pierrou S, Hellqvist M, Samuelsson L, et al. (1994). "Cloning and characterization of seven human forkhead proteins: binding site specificity and DNA bending.". EMBO J. 13 (20): 5002–12. PMID 7957066.
- Larsson C, Hellqvist M, Pierrou S, et al. (1997). "Chromosomal localization of six human forkhead genes, freac-1 (FKHL5), -3 (FKHL7), -4 (FKHL8), -5 (FKHL9), -6 (FKHL10), and -8 (FKHL12).". Genomics 30 (3): 464–9. doi:. PMID 8825632.
- Cederberg A, Betz R, Lagercrantz S, et al. (1997). "Chromosome localization, sequence analysis, and expression pattern identify FKHL 18 as a novel human forkhead gene.". Genomics 44 (3): 344–6. doi:. PMID 9325056.
- Freyaldenhoven BS, Fried C, Wielckens K (2003). "FOXD4a and FOXD4b, two new winged helix transcription factors, are expressed in human leukemia cell lines.". Gene 294 (1-2): 131–140. PMID 12234674.
- Fan Y, Newman T, Linardopoulou E, Trask BJ (2003). "Gene content and function of the ancestral chromosome fusion site in human chromosome 2q13-2q14.1 and paralogous regions.". Genome Res. 12 (11): 1663–72. doi:. PMID 12421752.
- 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:. PMID 12477932.
- Humphray SJ, Oliver K, Hunt AR, et al. (2004). "DNA sequence and analysis of human chromosome 9.". Nature 429 (6990): 369–74. doi:. PMID 15164053.
- 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:. PMID 15489334.
- Minoretti P, Arra M, Emanuele E, et al. (2007). "A W148R mutation in the human FOXD4 gene segregating with dilated cardiomyopathy, obsessive-compulsive disorder, and suicidality.". Int. J. Mol. Med. 19 (3): 369–72. PMID 17273782.

