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Gene : HMGN3 Homo sapiens

Name  ? high mobility group nucleosomal binding domain 3 Cytological Location  6q14.1
Brief Description  high mobility group nucleosomal binding domain 3
Description  The protein encoded by this gene binds thyroid hormone receptor beta in the presence of thyroid hormone. The encoded protein, a member of the HMGN protein family, is thought to reduce the compactness of the chromatin fiber in nucleosomes, thereby enhancing transcription from chromatin templates. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. There is a related pseudogene on chromosome 1. [provided by RefSeq, Jan 2016]
  • synonyms:
  • uc003pit.4,
  • HGNC:12312,
  • HMGN3,
  • NM_004242,
  • PNAS-24,
  • TRIP7,
  • OTTHUMG00000015073,
  • TRIP7,
  • thyroid hormone receptor interactor 7,
  • PNAS-25,
  • L40357
  • identifiers:
  • 9324,
  • ENSG00000118418,
  • HMGN3

Genome feature

Region: gene ? Length: 33438  
Location: 6:79201245-79234682 reverse strand Cyto location: 6q14.1

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0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Chromosomal location.

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Gene --> Proteins.


Gene Report --> GWAS hit


0 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Physical and Genetic Interactions


Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.



0 Pathways

715 SN Ps

5 Cross References

15 Data Sets

4 Homologues

0 Located Features

97 Rna Seq Results