Homo sapiens Protein: PRRX2
Summary
InnateDB Protein IDBP-89218.5
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol PRRX2
Protein Name paired related homeobox 2
Synonyms
Species Homo sapiens
Ensembl Protein ENSP00000361547
InnateDB Gene IDBG-89216 (PRRX2)
Protein Structure
UniProt Annotation
Function May play a role in the scarless healing of cutaneous wounds during the first two trimesters of development. {ECO:0000269PubMed:9665387}.
Subcellular Localization Nucleus {ECO:0000255PROSITE- ProRule:PRU00108, ECO:0000255PROSITE-ProRule:PRU00138}.
Disease Associations
Tissue Specificity In fetal skin, highest expression found in cells of mesodermal origin within the dermal papilla of the developing hair shaft. Not detected in epidermis or dermis. In adult skin, weakly expressed within the basal layers of the epidermis. Not expressed in dermis. {ECO:0000269PubMed:9665387}.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
Gene Ontology

Molecular Function
Accession GO Term
GO:0003677 DNA binding
GO:0003700 sequence-specific DNA binding transcription factor activity
GO:0043565 sequence-specific DNA binding
Biological Process
GO:0002053 positive regulation of mesenchymal cell proliferation
GO:0006355 regulation of transcription, DNA-templated
GO:0030326 embryonic limb morphogenesis
GO:0042472 inner ear morphogenesis
GO:0042474 middle ear morphogenesis
GO:0045880 positive regulation of smoothened signaling pathway
GO:0048701 embryonic cranial skeleton morphogenesis
GO:0048704 embryonic skeletal system morphogenesis
GO:0048844 artery morphogenesis
GO:0051216 cartilage development
Cellular Component
GO:0005634 nucleus
Protein Structure and Domains
PDB ID
InterPro IPR001356 Homeobox domain
IPR003654 OAR domain
IPR009057 Homeodomain-like
PFAM PF00046
PF03826
PRINTS
PIRSF
SMART SM00389
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q99811
PhosphoSite PhosphoSite-Q99811
TrEMBL
UniProt Splice Variant
Entrez Gene 51450
UniGene
RefSeq NP_057391
HUGO HGNC:21338
OMIM 604675
CCDS CCDS6926
HPRD 05244
IMGT
EMBL AF061970 AL590369 BC014645 CH471090 U81600
GenPept AAB39864 AAF17708 AAH14645 CAI14511 EAW87901