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Protein Coding Gene : Hmgn2 high mobility group nucleosomal binding domain 2

Primary Identifier  MGI:96136 Organism  mouse, laboratory
Chromosome  4 NCBI Gene Number  15331
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Predicted to enable chromatin binding activity. Acts upstream of or within negative regulation of transcription by RNA polymerase II and regulation of development, heterochronic. Located in female germ cell nucleus. Is expressed in several structures, including brain; eye; genitourinary system; heart; and lung. Orthologous to human HMGN2 (high mobility group nucleosomal binding domain 2).
PHENOTYPE: Mice homozygous for a knock-out allele are viable. [provided by MGI curators]
  • synonyms:
  • high mobility group nucleosomal binding domain 2,
  • HMG-17,
  • MGD-MRK-10772,
  • high mobility group protein 17,
  • Hmgn2,
  • Hmg17

Features --> Cross References

Genome

Sequence Feature Displayer

JG Browse Displayer

0 Canonical

0 CDSs

0 Exons

0 Genomic Clusters

4 Involved In Mutations

0 Strain

0 Transcripts

1 Transgenic Expressors

0 UTRs

Canonical gene --> CDSs in specific strains.

Canonical gene --> Exons in specific strains

Canonical gene --> Strain-specific IDs, biotypes, and locations

Canonical gene --> Transcripts in specific strains.

Features --> Overlapping features

Proteins

Gene --> Proteins

Function

Mouse features --> Functions (GO terms)

Homology

Genes --> Homologs

Interactions

0 Pathways

0 Targeted By

Gene --> Protein-Protein Interactions

Expression

Gene --> Expression annotations

Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

Literature

Mouse features --> Publications

 

Other

0 Driver For