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FOXD4 Identifiers Aliases FOXD4 , FKHL9, FOXD4A, FREAC-5, FREAC5, forkhead box D4External IDs OMIM : 601092 MGI : 1347467 HomoloGene : 83248 GeneCards : FOXD4 Gene location (Human ) Chr. Chromosome 9 (human) [1] Band 9p24.3 Start 116,231 bp [1] End 118,417 bp [1]
Gene location (Mouse ) Chr. Chromosome 19 (mouse)[2] Band 19 B|19 19.86 cM Start 24,876,600 bp [2] End 24,878,561 bp [2]
Gene ontology Molecular function Cellular component Biological process Sources:Amigo / QuickGO
Orthologs Species Human Mouse Entrez Ensembl UniProt RefSeq (mRNA) RefSeq (protein) Location (UCSC) Chr 9: 0.12 – 0.12 Mb Chr 19: 24.88 – 24.88 Mb PubMed search[3] [4] Wikidata
Forkhead box protein D4 is a protein that in humans is encoded by the FOXD4 gene .[5] [6] [7] [8]
References [ ]
^ a b c GRCh38: Ensembl release 89: ENSG00000170122 - Ensembl , May 2017
^ a b c GRCm38: Ensembl release 89: ENSMUSG00000051490 - 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 .
^ Pierrou S, Hellqvist M, Samuelsson L, Enerback S, Carlsson P (Dec 1994). "Cloning and characterization of seven human forkhead proteins: binding site specificity and DNA bending" . EMBO J . 13 (20): 5002–12. doi :10.1002/j.1460-2075.1994.tb06827.x . PMC 395442 . PMID 7957066 .
^
^ Freyaldenhoven BS, Fried C, Wielckens K (Sep 2002). "FOXD4a and FOXD4b, two new winged helix transcription factors, are expressed in human leukemia cell lines". Gene . 294 (1–2): 131–140. doi :10.1016/S0378-1119(02)00702-3 . PMID 12234674 .
^ "Entrez Gene: FOXD4 forkhead box D4" .
Further reading [ ]
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 :10.1006/geno.1997.4864 . PMID 9325056 .
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 :10.1101/gr.338402 . PMC 187549 . 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. Bibcode :2002PNAS...9916899M . doi :10.1073/pnas.242603899 . PMC 139241 . PMID 12477932 .
Humphray SJ, Oliver K, Hunt AR, et al. (2004). "DNA sequence and analysis of human chromosome 9" . Nature . 429 (6990): 369–74. Bibcode :2004Natur.429..369H . doi :10.1038/nature02465 . PMC 2734081 . 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 :10.1101/gr.2596504 . PMC 528928 . 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. doi :10.3892/ijmm.19.3.369 . PMID 17273782 .
Categories :
Genes on human chromosome 9 Forkhead transcription factors Human chromosome 9 gene stubs