HMGB4

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

HMGB4
Identifiers
AliasesHMGB4, dJ1007G16.5, high mobility group box 4
External IDsOMIM: 617285 MGI: 1916567 HomoloGene: 83321 GeneCards: HMGB4
Gene location (Human)
Chr.Chromosome 1 (human)[1]
Band1p35.1Start33,860,475 bp[1]
End33,864,791 bp[1]
Orthologs
SpeciesHumanMouse
Entrez

127540

69317

Ensembl

ENSG00000176256

ENSMUSG00000048686

UniProt

Q8WW32

Q6P8W9

RefSeq (mRNA)

NM_145205
NM_001352984
NM_001379301

NM_027036

RefSeq (protein)

NP_660206
NP_001339913
NP_001366230

NP_081312

Location (UCSC)Chr 1: 33.86 – 33.86 MbChr 4: 128.26 – 128.26 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

See also

References

  1. GRCh38: Ensembl release 89: ENSG00000176256 - Ensembl, May 2017
  2. GRCm38: Ensembl release 89: ENSMUSG00000048686 - Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. "Entrez Gene: high-mobility group box 4".

Further reading


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