Homo sapiens Protein: LHX3
Summary
InnateDB Protein IDBP-92195.7
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol LHX3
Protein Name LIM homeobox 3
Synonyms CPHD3; LIM3; M2-LHX3;
Species Homo sapiens
Ensembl Protein ENSP00000360811
InnateDB Gene IDBG-92191 (LHX3)
Protein Structure
UniProt Annotation
Function Acts as a transcriptional activator. Binds to and activates the promoter of the alpha-glycoprotein gene, and synergistically enhances transcription from the prolactin promoter in cooperation with POU1F1/Pit-1 (By similarity). Required for the establishment of the specialized cells of the pituitary gland and the nervous system. Involved in the development of interneurons and motor neurons in cooperation with LDB1 and ISL1. {ECO:0000250, ECO:0000269PubMed:21149718}.
Subcellular Localization Nucleus {ECO:0000305}.
Disease Associations Pituitary hormone deficiency, combined, 3 (CPHD3) [MIM:221750]: Combined pituitary hormone deficiency is defined as the impaired production of growth hormone and one or more of the other five anterior pituitary hormones. CPHD3 is characterized by a complete deficit in all but one (adrenocorticotropin) anterior pituitary hormone and a rigid cervical spine leading to limited head rotation. {ECO:0000269PubMed:10835633, ECO:0000269PubMed:17327381}. 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 9 experimentally validated interaction(s) in this database.
They are also associated with 2 interaction(s) predicted by orthology.
Experimentally validated
Total 9 [view]
Protein-Protein 9 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 2 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0001076 RNA polymerase II transcription factor binding transcription factor activity
GO:0003677 DNA binding
GO:0003700 sequence-specific DNA binding transcription factor activity
GO:0005515 protein binding
GO:0008270 zinc ion binding
GO:0043565 sequence-specific DNA binding
Biological Process
GO:0001890 placenta development
GO:0006366 transcription from RNA polymerase II promoter
GO:0008045 motor neuron axon guidance
GO:0009887 organ morphogenesis
GO:0009953 dorsal/ventral pattern formation
GO:0021520 spinal cord motor neuron cell fate specification
GO:0021521 ventral spinal cord interneuron specification
GO:0021526 medial motor column neuron differentiation
GO:0021527 spinal cord association neuron differentiation
GO:0021983 pituitary gland development
GO:0030154 cell differentiation
GO:0030324 lung development
GO:0043066 negative regulation of apoptotic process
GO:0045893 positive regulation of transcription, DNA-templated
GO:0045944 positive regulation of transcription from RNA polymerase II promoter
GO:0048839 inner ear development
Cellular Component
GO:0005622 intracellular
GO:0005634 nucleus
GO:0005667 transcription factor complex
Protein Structure and Domains
PDB ID
InterPro IPR001356 Homeobox domain
IPR001781 Zinc finger, LIM-type
IPR009057 Homeodomain-like
PFAM PF00046
PF00412
PRINTS
PIRSF
SMART SM00389
SM00132
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q9UBR4
PhosphoSite PhosphoSite-Q9UBR4
TrEMBL F1T0D9
UniProt Splice Variant
Entrez Gene 8022
UniGene
RefSeq NP_055379
HUGO HGNC:6595
OMIM 600577
CCDS CCDS6995
HPRD 02783
IMGT
EMBL AB593065 AB593066 AF096169 AF156888 AF156889 AF214637 AF367085 AF367086 AF367087 AF367088 AF367089 AH008761 AL138781 CH471090
GenPept AAF17291 AAF17292 AAF26412 AAF36808 AAF36809 AAL26314 BAJ84012 BAJ84013 CAI16878 CAI16879 EAW88205 EAW88206