Polycomb protein EED

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

Polycomb protein EED is a protein that in humans is encoded by the EED gene.[5][6][7]

PDBOrtholog search: PDBe RCSB
AliasesEED, HWAIT1, embryonic ectoderm development, COGIS
Quick facts EED, Available structures ...
EED
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesEED, HWAIT1, embryonic ectoderm development, COGIS
External IDsOMIM: 605984; MGI: 95286; HomoloGene: 2814; GeneCards: EED; OMA:EED - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001308007
NM_003797
NM_152991
NM_001330334

NM_021876

RefSeq (protein)

NP_001294936
NP_001317263
NP_003788

NP_068676

Location (UCSC)Chr 11: 86.24 – 86.28 MbChr 7: 89.6 – 89.63 Mb
PubMed search[3][4]
Wikidata
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Function

Polycomb protein EED is a member of the Polycomb-group (PcG) family. PcG family members form multimeric protein complexes, which are involved in maintaining the transcriptional repressive state of genes over successive cell generations. This protein interacts with enhancer of zeste 2, the cytoplasmic tail of integrin β7, immunodeficiency virus type 1 (HIV-1) MA protein, and histone deacetylase proteins. This protein mediates repression of gene activity through histone deacetylation, and may act as a specific regulator of integrin function. Two transcript variants encoding distinct isoforms have been identified for this gene.[7]

Clinical significance

In humans, a de-novo mutation in EED has been reported in an individual displaying symptoms similar to those of Weaver syndrome.[8]

Interactions

EED has been shown to interact with:

References

Further reading

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