|  Help  |  About  |  Contact Us

Protein Coding Gene : Pbxip1 pre B cell leukemia transcription factor interacting protein 1

Primary Identifier  MGI:2441670 Organism  mouse, laboratory
Chromosome  3 NCBI Gene Number  229534
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Enables transcription coactivator activity. Acts upstream of or within several processes, including articular cartilage development; extracellular matrix organization; and positive regulation of chondrocyte proliferation. Located in cytoplasm and nucleus. Part of chromatin and transcription regulator complex. Is expressed in brain; diaphragm; gut; heart ventricle; and spinal cord ventricular layer. Orthologous to human PBXIP1 (PBX homeobox interacting protein 1).
PHENOTYPE: Mice homozygous for a null allele exhibit proportional dwafism. Mice homozygous for a conditional allele activated in chondrocytes exhibit improved induced pathogenic osteoarthritis. [provided by MGI curators]
  • synonyms:
  • pre B cell leukemia transcription factor interacting protein 1,
  • Pbxip1,
  • RIKEN cDNA 4732463H20 gene,
  • 4732463H20Rik

Features --> Cross References

Genome

Sequence Feature Displayer

JG Browse Displayer

0 Canonical

0 CDSs

0 Exons

0 Genomic Clusters

2 Involved In Mutations

0 Strain

0 Transcripts

0 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