Homo sapiens Protein: PROP1
Summary
InnateDB Protein IDBP-60640.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol PROP1
Protein Name PROP paired-like homeobox 1
Synonyms CPHD2; PROP-1;
Species Homo sapiens
Ensembl Protein ENSP00000311290
InnateDB Gene IDBG-60638 (PROP1)
Protein Structure
UniProt Annotation
Function Possibly involved in the ontogenesis of pituitary gonadotropes, as well as somatotropes, lactotropes and caudomedial thyrotropes.
Subcellular Localization Nucleus {ECO:0000255PROSITE- ProRule:PRU00108}.
Disease Associations Pituitary hormone deficiency, combined, 2 (CPHD2) [MIM:262600]: Combined pituitary hormone deficiency is defined as the impaired production of growth hormone and one or more of the other five anterior pituitary hormones. CPHD2 is characterized by pleiotropic deficiencies of growth hormone, thyroid-stimulating hormone, follicle-stimulating hormone, luteinizing hormone, prolactin and adrenocorticotropic hormone. {ECO:0000269PubMed:10946881, ECO:0000269PubMed:11549703, ECO:0000269PubMed:12519826, ECO:0000269PubMed:15531542, ECO:0000269PubMed:19128366, ECO:0000269PubMed:9462743, ECO:0000269PubMed:9768691}. Note=The disease is caused by mutations affecting the gene represented in this entry.
Tissue Specificity Expressed specifically in embryonic pituitary.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 12 experimentally validated interaction(s) in this database.
They are also associated with 5 interaction(s) predicted by orthology.
Experimentally validated
Total 12 [view]
Protein-Protein 12 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 5 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0000976 transcription regulatory region sequence-specific DNA binding
GO:0003677 DNA binding
GO:0003682 chromatin binding
GO:0003700 sequence-specific DNA binding transcription factor activity
GO:0005515 protein binding
GO:0008013 beta-catenin binding
GO:0008022 protein C-terminus binding
Biological Process
GO:0000122 negative regulation of transcription from RNA polymerase II promoter
GO:0001568 blood vessel development
GO:0007417 central nervous system development
GO:0009887 organ morphogenesis
GO:0009953 dorsal/ventral pattern formation
GO:0016477 cell migration
GO:0021979 hypothalamus cell differentiation
GO:0021984 adenohypophysis development
GO:0043066 negative regulation of apoptotic process
GO:0045944 positive regulation of transcription from RNA polymerase II promoter
GO:0048732 gland development
GO:0048850 hypophysis morphogenesis
GO:0060070 canonical Wnt signaling pathway
GO:0060126 somatotropin secreting cell differentiation
Cellular Component
GO:0005634 nucleus
GO:0005667 transcription factor complex
Protein Structure and Domains
PDB ID
InterPro IPR000047 Helix-turn-helix motif
IPR001356 Homeobox domain
IPR009057 Homeodomain-like
PFAM PF00046
PRINTS PR00031
PIRSF
SMART SM00389
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt O75360
PhosphoSite PhosphoSite-O75360
TrEMBL
UniProt Splice Variant
Entrez Gene 5626
UniGene Hs.158301
RefSeq NP_006252
HUGO HGNC:9455
OMIM 601538
CCDS CCDS4430
HPRD 03325
IMGT
EMBL AC136940 AF041139 AF041140 AF041141 AF076214 AF076215 BC069076
GenPept AAC27900 AAC77453 AAC77454 AAH69076