HMG20A

HMG20A
Identifiers
Aliases	HMG20A, HMGX1, HMGXB1, high mobility group 20A
External IDs	MGI: 1914117 HomoloGene: 32399 GeneCards: HMG20A
Gene location (Human)
Chr.	Chromosome 15 (human)[1]
End	77,485,607 bp[1]
Gene location (Mouse)
Chr.	Chromosome 9 (mouse)[2]
End	56,496,936 bp[2]
RNA expression pattern
	More reference expression data
Gene ontology
Molecular function	• transcription factor activity, sequence-specific DNA binding; • protein heterodimerization activity; • DNA binding; • protein binding; • identical protein binding; • RNA polymerase II transcription factor activity, sequence-specific DNA binding;
Cellular component	• cell nucleus;
Biological process	• regulation of transcription, DNA-templated; • negative regulation of transcription from RNA polymerase II promoter; • negative regulation of neuron differentiation; • transcription, DNA-templated; • negative regulation of protein sumoylation; • chromatin organization;
	Sources:Amigo / QuickGO
Orthologs
	10363
	66867
	ENSG00000140382
	ENSMUSG00000032329
	Q9NP66
	Q9DC33
	NM_001304504; NM_001304505; NM_018200
	NM_025812
	NP_001291433; NP_001291434; NP_060670
	NP_080088
	Wikidata
View/Edit Human	View/Edit Mouse

High mobility group protein 20A is a protein that in humans is encoded by the HMG20A gene.^[5]^[6]

References

1 2 3 GRCh38: Ensembl release 89: ENSG00000140382 - Ensembl, May 2017
1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000032329 - Ensembl, May 2017
↑ "Human PubMed Reference:".
↑ "Mouse PubMed Reference:".
↑ Sumoy L, Carim L, Escarceller M, Nadal M, Gratacòs M, Pujana MA, Estivill X, Peral B (Jun 2000). "HMG20A and HMG20B map to human chromosomes 15q24 and 19p13.3 and constitute a distinct class of HMG-box genes with ubiquitous expression". Cytogenetics and Cell Genetics. 88 (1–2): 62–7. doi:10.1159/000015486. PMID 10773667.
↑ "Entrez Gene: HMG20A high-mobility group 20A".

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