HMGB4

HMGB4
Identifiers
Aliases	HMGB4, dJ1007G16.5, high mobility group box 4
External IDs	MGI: 1916567 HomoloGene: 83321 GeneCards: HMGB4
Gene location (Human)
Chr.	Chromosome 1 (human)[1]
End	33,864,791 bp[1]
Gene location (Mouse)
Chr.	Chromosome 4 (mouse)[2]
End	128,260,957 bp[2]
Orthologs
	127540
	69317
	ENSG00000176256
	ENSMUSG00000048686
	Q8WW32
	Q6P8W9
	NM_145205; NM_001352984
	NM_027036
	NP_660206; NP_001339913
	NP_081312
	Wikidata
View/Edit Human	View/Edit Mouse

High mobility group protein B4 is a transcription factor that in humans is encoded by the HMGB4 gene.^[5]

References

Strausberg RL, Feingold EA, Grouse LH, et al. (2002). "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.
Sogayar MC, Camargo AA, Bettoni F, et al. (2004). "A transcript finishing initiative for closing gaps in the human transcriptome". Genome Res. 14 (7): 1413–23. doi:10.1101/gr.2111304. PMC 442158. PMID 15197164.
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.
Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. 36 (1): 40–5. doi:10.1038/ng1285. PMID 14702039.

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