HMG20B

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily E member 1-related is a protein that in humans is encoded by the HMG20B gene.[5][6]

PDBOrtholog search: PDBe RCSB
AliasesHMG20B, BRAF25, BRAF35, HMGX2, HMGXB2, PP7706, SMARCE1r, SOXL, pp8857, high mobility group 20B
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HMG20B
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesHMG20B, BRAF25, BRAF35, HMGX2, HMGXB2, PP7706, SMARCE1r, SOXL, pp8857, high mobility group 20B
External IDsOMIM: 605535; MGI: 1341190; HomoloGene: 74949; GeneCards: HMG20B; OMA:HMG20B - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_006339

NM_001163165
NM_001163166
NM_010440

RefSeq (protein)

NP_006330

NP_001156637
NP_001156638
NP_034570

Location (UCSC)Chr 19: 3.57 – 3.58 MbChr 10: 81.18 – 81.19 Mb
PubMed search[3][4]
Wikidata
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HMG20B is a high-mobility group (HMG) DNA binding protein. HMG20B contains a carboxy terminal region that is essential for cytokinesis since it regulates cell cycle progression from the G2 phase into mitosis[7] This carboxy terminal region of HMG20B interacts with the tumor suppressor protein BRCA2. A particular mutation in this region of the HMG20B gene is associated with lung cancer. This mutation interferes with the association of the HMG20B and BRCA2 proteins.[7]

Interactions

HMG20B has been shown to interact with:

References

Further reading

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