1. Gene
  2. BSX - brain specific homeobox Gene

BSX - brain specific homeobox Gene

Homo sapiens

Also known as BSX1

Gene ID: 390259 | Gene type: protein coding

About BSX

Cytogenetic location: 11q24.1 Genomic coordinates (GRCh38): 11:122,977,570-122,981,834 (from NCBI)

This gene has 1 transcript (splice variant), 126 orthologues and 9 paralogues. Low expression observed in reference dataset.

Summary

Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to act upstream of or within several processes, including eating behavior; mammary gland involution; and positive regulation of transcription by RNA polymerase II. Predicted to be located in cytoplasm. Predicted to be part of chromatin. [provided by Alliance of Genome Resources, Apr 2022]

BSX Products(1)

mRNA Protein Name
NM_001098169.2 NP_001091639.1 brain-specific homeobox protein homolog
Gene Ontology
  • Molecular Function
Molecular Function GO Annotation Evidence Reference Source
enables sequence-specific double-stranded DNA binding IDA
IDA: Inferred from direct assay
28473536 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

BSX Protein Structure

Homeobox

Homeobox: Homeobox domain (111 - 167)

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

brain-specific homeobox protein homolog

Related Diseases

Diseases Alias
Jacobsen Syndrome

Chromosome 11q Deletion Syndrome

Partial 11q Monosomy Syndrome

Jacobsen Distal 11q Deletion Syndrome

JBS

11q Partial Monosomy Syndrome

Chromosome 11q Deletion

11q Deletion

11q Monosomy

Deletion 11q

Monosomy 11q

Partial Monosomy 11q

11q Deletion Disorder

11q Deletion Syndrome

11q Terminal Deletion Disorder

11q- Deletion Syndrome

11q23 Deletion Disorder

Jacobsen Thrombocytopenia

11q Terminal Deletion Syndrome

Del(11)(Q23.3)

Del(11)(Qter)

Distal Deletion 11q

Distal Monosomy 11q

Monosomy 11qter

Telomeric Deletion 11q

Paris-Trousseau Thrombocytopenia

Exocervical Carcinoma

Carcinoma Of Exocervix

Carcinoma Of The Exocervix

Autoimmune Glomerulonephritis
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
Rattus norvegicus BSX RGD RGD:1565120
Canis familiaris BSX VGNC VGNC:38543
Macaca mulatta BSX VGNC VGNC:107427
Felis catus BSX VGNC VGNC:60192
Bos taurus BSX VGNC VGNC:26582
Mus musculus BSX MGD MGI:2669849