HOXB3 Gene Summary [Human]

This gene is a member of the Antp homeobox family and encodes a nuclear protein with a homeobox DNA-binding domain. It is included in a cluster of homeobox B genes located on chromosome 17. The encoded protein functions as a sequence-specific transcription factor that is involved in development. Increased expression of this gene is associated with a distinct biologic subset of acute myeloid leukemia (AML). [provided by RefSeq, Jul 2008]

Details

Type
Protein Coding
Official Symbol
HOXB3
Official Name
homeobox B3 [Source:HGNC Symbol;Acc:HGNC:5114]
Ensembl ID
ENSG00000120093
Bio databases IDs NCBI: 3213 Ensembl: ENSG00000120093
Aliases homeobox B3
Synonyms homeo box B3, HOX2, Hox-2.7, HOX2G
Species
Human, Homo sapiens
OrthologiesMouseRat

Protein Domains

A protein domain is a distinct structural or functional region within a protein that can evolve, function, and exist independently of the rest of the protein chain. These domains in human HOXB3 often fold into stable, three-dimensional structures and are associated with specific biological functions, such as binding to DNA, other proteins, or small molecules.
  • RNA polymerase II transcription regulatory region sequence-specific binding transcriptional activator activity
  • RNA polymerase II transcription factor activity, sequence-specific DNA binding
  • transcription regulator
  • Domain of unknown function (DUF4074)
  • double-stranded DNA binding
  • nucleic acid binding
  • homeolike domain
  • sequence-specific DNA binding
  • homeodomain

Pathways

Biological processes and signaling networks where the HOXB3 gene in human plays a role, providing insight into its function and relevance in health or disease.

Top Findings

The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
disease
  • obesity
  • insomnia
  • glossopharyngeal-vagus nerve fusion
  • acute myeloid leukemia
  • diverticular disease
  • cleft lip
  • overnutrition
  • Cornelia de Lange syndrome
regulated by
regulates
role in cell
  • proliferation
  • number
  • differentiation
  • cell cycle progression
  • colony formation
  • quantity
  • transcription in
  • transactivation in
  • morphogenesis in

Subcellular Expression

Locations within the cell where the protein is known or predicted to be active, providing insight into its function and cellular context.
  • Nucleus
  • nucleoplasm
  • chromatin

Gene Ontology Annotations

Describes the biological processes, cellular components, and molecular functions associated with the human HOXB3 gene, providing context for its role in the cell.

Biological Process

Functions and activities the gene product is involved in
  • glossopharyngeal nerve morphogenesis
  • anterior/posterior pattern specification
  • rhombomere development
  • positive regulation of transcription from RNA polymerase II promoter
  • face development
  • hemopoietic progenitor cell differentiation
  • embryonic skeletal system morphogenesis
  • regulation of transcription from RNA polymerase II promoter
  • definitive hemopoiesis
  • negative regulation of transcription from RNA polymerase II promoter
  • thyroid gland development
  • angiogenesis
  • regulation of neurogenesis
  • cartilage development

Cellular Component

Where in the cell the gene product is active
  • nucleus
  • chromatin
  • nucleoplasm

Molecular Function

What the gene product does at the molecular level
  • RNA polymerase II core promoter proximal region sequence-specific DNA binding
  • RNA polymerase II transcription regulatory region sequence-specific DNA binding transcription factor activity involved in positive regulation of transcription
  • sequence-specific DNA binding RNA polymerase II transcription factor activity

Gene-Specific Assays for Results You Can Trust

Streamline your workflow with assays designed for this gene. Our targeted dPCR and qPCR assays help you generate meaningful data – efficiently and accurately.