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Gene : HMGN4 Homo sapiens

Name  ? high mobility group nucleosomal binding domain 4 Cytological Location  6p22.2
Brief Description  high mobility group nucleosomal binding domain 4
Description  The protein encoded by this gene, 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. [provided by RefSeq, Mar 2013]
  • synonyms:
  • HMG17L3,
  • NHC,
  • high-mobility group (nonhistone chromosomal) protein 17-like 3,
  • NHC,
  • HGNC:4989,
  • uc003nig.4,
  • U90549,
  • HMG17L3,
  • HMGN4,
  • NM_006353,
  • OTTHUMG00000014458
  • identifiers:
  • 10473,
  • ENSG00000182952,
  • HMGN4

Genome feature

Region: gene ? Length: 8587  
Location: 6:26538347-26546933 Cyto location: 6p22.2


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Function

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0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Genomics

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Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.

Proteins

Gene --> Proteins.

SNPs

Gene Report --> GWAS hit

Disease

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]

Homology

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Interactions

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Gene --> Physical and Genetic Interactions

Expression

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

Gene Ontology

Gene --> GO terms.

 

Other

0 Pathways

3753 SN Ps

4 Cross References

14 Data Sets

2 Homologues

0 Located Features

97 Rna Seq Results