HMGB3 - high mobility group box 3 Gene

Also Known as HMG4; HMG-4; HMG2A; HMG-2a

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 3149

About HMGB3

Cytogenetic location: Xq28 Genomic coordinates (GRCh38): X:150,980,507-150,990,771 (from NCBI)

This gene has 5 transcripts (splice variants), 198 orthologues, 20 paralogues and is associated with 2 phenotypes. Broad expression in placenta (RPKM 24.9), bone marrow (RPKM 7.8) and 21 other tissues.

Summary

This gene encodes a member of a family of proteins containing one or more high mobility group DNA-binding motifs. The encoded protein plays an important role in maintaining stem cell populations, and may be aberrantly expressed in tumor cells. A mutation in this gene was associated with microphthalmia, syndromic 13. There are numerous pseudogenes of this gene on multiple chromosomes. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]

HMGB3 Products (4)

mRNA Protein Name
NM_001301228.2 NP_001288157.1 high mobility group protein B3 isoform a
NM_001301229.2 NP_001288158.1 high mobility group protein B3 isoform a
NM_001301231.2 NP_001288160.1 high mobility group protein B3 isoform b
NM_005342.4 NP_005333.2 high mobility group protein B3 isoform a
Molecular Function GO Annotation Evidence References Source
enables protein binding IPI
IPI: Inferred from physical interaction
21044950 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

HMGB3 Protein Structure

HMG_box_2

HMG_box_2: HMG-box domain (6 - 78)

HMG_box

HMG_box: HMG (high mobility group) box (93 - 161)

  • 0
  • 100
  • 200 a.a.
Protein Preferred Names Protein Names

high mobility group protein B3

  • high mobility group protein 2a

HMGB3 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
HMGB3 O15347 MEOX2 Homo sapiens Q6FHY5 32296183
Intra
HMGB3 O15347 MEOX2 Homo sapiens Q6FHY5 32296183
Intra
HMGB3 O15347 MEOX2 Homo sapiens Q6FHY5 32296183
Intra
HMGB3 O15347 MEOX1 Homo sapiens P50221 32296183
Intra
HMGB3 O15347 MEOX1 Homo sapiens P50221 32296183
Intra
HMGB3 O15347 MEOX1 Homo sapiens P50221 32296183
Intra
HMGB3 O15347 PAX5 Homo sapiens Q02548 32296183
Intra
HMGB3 O15347 PAX5 Homo sapiens Q02548 32296183
Intra
HMGB3 O15347 PAX5 Homo sapiens Q02548 32296183
Intra
HMGB3 O15347 SDCBP Homo sapiens O00560 31515488
Intra
HMGB3 O15347 SDCBP Homo sapiens O00560 25416956
Intra
HMGB3 O15347 SDCBP Homo sapiens O00560 32296183
Intra
HMGB3 O15347 SDCBP Homo sapiens O00560 32296183
Intra
HMGB3 O15347 PAX6 Homo sapiens P26367 32296183
Intra
HMGB3 O15347 PAX6 Homo sapiens P26367 32296183
Intra
HMGB3 O15347 PAX6 Homo sapiens P26367 32296183
Intra
HMGB3 O15347 TERF2IP Homo sapiens Q9NYB0 21044950
Intra
HMGB3 O15347 TERF2IP Homo sapiens Q9NYB0 21044950
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant HMGB3 Proteins

Cat. No. Product Name Accession Purity
HY-P70199 HMGB3/HMG-3 Protein, Human (HEK293, His) O15347 (M1-E200) ≥ 95%, as determined by reducing SDS-PAGE.

HMGB3 Antibodies

Cat. No. Product Name Application Reactivity
HY-P83247 HMG4 Antibody (YA2992) WB, IHC-P, ICC/IF, FC, IP Human, Mouse, Rat
HY-P83247A HMG4 Antibody (YA2992)(PBS only) WB, IHC-P, ICC/IF, FC, IP Human, Mouse, Rat

Related Diseases

Diseases Alias
Microphthalmia, Syndromic 13
  • X-Linked Colobomatous Microphthalmia-Microcephaly-Intellectual Disability-Short Stature Syndrome

  • MCOPS13

  • Maine Microphthalmos

  • Colobomatous Microphthalmia With Microcephaly, Short Stature, And Psychomotor Retardation

  • Syndromic Microphthalmia 13

  • X-Linked Colobomatous Microphthalmia-Microcephaly-Short Stature-Psychomotor Retardation Syndrome

  • Microphthalmia, Syndromic, 13

  • Microphthalmia, Syndromic, Type 13

Microphthalmia
  • Microphthalmos

  • Isolated Anophthalmia-Microphthalmia Syndrome

  • Isolated Microphthalmia-Anophthalmia-Coloboma

  • Simple Microphthalmos

  • Clinical Anophthalmia

  • Isolated Anophthalmia - Microphthalmia

  • Isolated Pure Microphthalmia

  • Mac Spectrum

  • Microphthalmia-Anophthalmia-Coloboma Spectrum

  • Primitive Anophthalmia

  • Globe Of Eye Small

  • Small Eyeball

  • Hypoplasia Of Eye

  • Isolated Nanophthalmos

  • Rudimentary Eye

  • Dysplasia Of Eye

Terminal Osseous Dysplasia
  • Terminal Osseous Dysplasia And Pigmentary Defects

  • Terminal Osseous Dysplasia-Pigmentary Defects Syndrome

  • Todpd

  • TOD

  • Odpd

  • Odpf Syndrome

  • Osseous Dysplasia, Digital, With Facial Pigmentary Defects And Multiple Frenula

  • Odpf

  • Digital Osseous Dysplasia With Facial Pigmentary Defects And Multiple Frenula

  • Terminal Osseous Dysplasia With Pigmentary Defects

  • Dcd

  • Digitocutaneous Dysplasia

  • Terminal Osseous Dysplasia And Pigmentary Defect Syndrome

  • Osseous Dysplasia And Pigmentary Defects

Microcephaly
  • Microencephaly

  • Microcephalus

  • Microcephalic

  • Nanocephaly

  • Congenital Microcephaly

  • Brain Hypoplasia

  • Brain Nondevelopment

  • Cephalic Hypoplasia

  • Undeveloped Cerebrum

  • Undeveloped Brain

  • Micrencephalon

  • Micrencephaly

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Mus musculus HMGB3 MGD MGI:1098219
Rattus norvegicus HMGB3 RGD RGD:1564407
Canis familiaris HMGB3 VGNC VGNC:54164
Others HMGB3 NCBI