Homo sapiens Protein: PAX1
Summary
InnateDB Protein IDBP-232980.5
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol PAX1
Protein Name paired box 1
Synonyms HUP48; OFC2;
Species Homo sapiens
Ensembl Protein ENSP00000381499
InnateDB Gene IDBG-59158 (PAX1)
Protein Structure
UniProt Annotation
Function This protein is a transcriptional activator. It may play a role in the formation of segmented structures of the embryo. May play an important role in the normal development of the vertebral column (By similarity). {ECO:0000250}.
Subcellular Localization Nucleus.
Disease Associations Otofaciocervical syndrome 2 (OFC2) [MIM:615560]: A disorder characterized by facial dysmorphism, cup-shaped low-set ears, preauricular fistulas, hearing loss, branchial defects, skeletal anomalies including vertebral defects, low-set clavicles, winged scapulae, sloping shoulders, and mild intellectual disability. {ECO:0000269PubMed:23851939}. Note=The disease is caused by mutations affecting the gene represented in this entry.
Tissue Specificity
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 4 experimentally validated interaction(s) in this database.
They are also associated with 3 interaction(s) predicted by orthology.
Experimentally validated
Total 4 [view]
Protein-Protein 3 [view]
Protein-DNA 1 [view]
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 3 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0003677 DNA binding
Biological Process
GO:0001501 skeletal system development
GO:0001756 somitogenesis
GO:0006355 regulation of transcription, DNA-templated
GO:0006366 transcription from RNA polymerase II promoter
GO:0007389 pattern specification process
GO:0008283 cell proliferation
GO:0043367 CD4-positive, alpha-beta T cell differentiation
GO:0043374 CD8-positive, alpha-beta T cell differentiation
GO:0045944 positive regulation of transcription from RNA polymerase II promoter
GO:0048538 thymus development
GO:0060017 parathyroid gland development
GO:0060349 bone morphogenesis
GO:0061056 sclerotome development
Cellular Component
GO:0005634 nucleus
Protein Structure and Domains
PDB ID
InterPro IPR001523 Paired domain
IPR009057 Homeodomain-like
PFAM PF00292
PRINTS PR00027
PIRSF
SMART SM00351
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt P15863
PhosphoSite PhosphoSite-P15863
TrEMBL
UniProt Splice Variant
Entrez Gene 5075
UniGene Hs.122310
RefSeq NP_006183
HUGO HGNC:8615
OMIM 167411
CCDS CCDS13146
HPRD 01332
IMGT
EMBL AK303335 AL035562 AY740018 BC069134 X15044
GenPept AAH69134 AAU21037 BAG64398 CAA33146 CAB46996 CAX12115