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Gene Gene information from NCBI Gene database.
Entrez ID 9324
Gene name High mobility group nucleosomal binding domain 3
Gene symbol HMGN3
Synonyms (NCBI Gene)
PNAS-24PNAS-25TRIP7
Chromosome 6
Chromosome location 6q14.1
Summary 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 enhancin
miRNA miRNA information provided by mirtarbase database.
131 Show/Hide all (131)
miRTarBase ID miRNA Experiments Reference
MIRT557266 hsa-miR-5580-3p PAR-CLIP 21572407
MIRT557267 hsa-miR-5011-5p PAR-CLIP 21572407
MIRT557265 hsa-miR-511-3p PAR-CLIP 21572407
MIRT557263 hsa-miR-3177-5p PAR-CLIP 21572407
MIRT557264 hsa-miR-6867-5p PAR-CLIP 21572407
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
12 Show/Hide all (12)
GO ID Ontology Definition Evidence Reference
GO:0000785 Component Chromatin IEA
GO:0003677 Function DNA binding IEA
GO:0003682 Function Chromatin binding IBA
GO:0005515 Function Protein binding IPI 33468658
GO:0005634 Component Nucleus IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
604502 12312 ENSG00000118418
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q15651
Protein name High mobility group nucleosome-binding domain-containing protein 3 (Thyroid receptor-interacting protein 7) (TR-interacting protein 7) (TRIP-7)
Protein function Binds to nucleosomes, regulating chromatin structure and consequently, chromatin-dependent processes such as transcription, DNA replication and DNA repair. Affects both insulin and glucagon levels and modulates the expression of pancreatic genes
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01101 HMG14_17 1 → 97 HMG14 and HMG17 Family
Tissue specificity TISSUE SPECIFICITY: Expressed in kidney, lung, pancreas, testis, skeletal muscle, heart, thyroid gland, pituitary gland, prostate and uterus. Low expression in liver, spleen, placenta and ovaries. {ECO:0000269|PubMed:11356838, ECO:0000269|PubMed:7776974}.
Sequence
Sequence length 99
Interactions View interactions