Homo sapiens Protein: GLI2
Summary
InnateDB Protein IDBP-68276.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol GLI2
Protein Name GLI family zinc finger 2
Synonyms HPE9; PHS2; THP1; THP2;
Species Homo sapiens
Ensembl Protein ENSP00000354586
InnateDB Gene IDBG-68270 (GLI2)
Protein Structure
UniProt Annotation
Function Acts as a transcriptional activator. May play a role during embryogenesis. Binds to the DNA sequence 5'-GAACCACCCA-3' which is part of the TRE-2S regulatory element that augments the Tax-dependent enhancer of human T-cell leukemia virus type 1. Is involved in the smoothened (SHH) signaling pathway. {ECO:0000269PubMed:18455992}.
Subcellular Localization Nucleus {ECO:0000250}. Cytoplasm {ECO:0000250}. Note=In keratinocytes, it is sequestered in the cytoplasm by SUFU. In the absence of SUFU, it translocates to the nucleus (By similarity). {ECO:0000250}.
Disease Associations Holoprosencephaly 9 (HPE9) [MIM:610829]: A structural anomaly of the brain, in which the developing forebrain fails to correctly separate into right and left hemispheres. Holoprosencephaly is genetically heterogeneous and associated with several distinct facies and phenotypic variability. Holoprosencephaly type 9 is characterized by defective anterior pituitary formation and pan-hypopituitarism, with or without overt forebrain cleavage abnormalities, and holoprosencephaly-like midfacial hypoplasia. {ECO:0000269PubMed:14581620, ECO:0000269PubMed:17096318}. 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 20 experimentally validated interaction(s) in this database.
They are also associated with 12 interaction(s) predicted by orthology.
Experimentally validated
Total 20 [view]
Protein-Protein 11 [view]
Protein-DNA 9 [view]
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 12 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0003700 sequence-specific DNA binding transcription factor activity
GO:0005515 protein binding
GO:0008270 zinc ion binding
GO:0043565 sequence-specific DNA binding
GO:0046872 metal ion binding
Biological Process
GO:0000122 negative regulation of transcription from RNA polymerase II promoter
GO:0001501 skeletal system development
GO:0001649 osteoblast differentiation
GO:0001822 kidney development
GO:0002076 osteoblast development
GO:0006351 transcription, DNA-templated
GO:0006355 regulation of transcription, DNA-templated
GO:0007224 smoothened signaling pathway
GO:0007389 pattern specification process
GO:0007411 axon guidance
GO:0007418 ventral midline development
GO:0007442 hindgut morphogenesis
GO:0007507 heart development
GO:0008283 cell proliferation
GO:0009913 epidermal cell differentiation
GO:0009954 proximal/distal pattern formation
GO:0021508 floor plate formation
GO:0021513 spinal cord dorsal/ventral patterning
GO:0021517 ventral spinal cord development
GO:0021696 cerebellar cortex morphogenesis
GO:0021775 smoothened signaling pathway involved in ventral spinal cord interneuron specification
GO:0021965 spinal cord ventral commissure morphogenesis
GO:0021983 pituitary gland development
GO:0030324 lung development
GO:0030879 mammary gland development
GO:0030902 hindbrain development
GO:0033089 positive regulation of T cell differentiation in thymus
GO:0035295 tube development
GO:0042475 odontogenesis of dentin-containing tooth
GO:0045740 positive regulation of DNA replication
GO:0045893 positive regulation of transcription, DNA-templated
GO:0045944 positive regulation of transcription from RNA polymerase II promoter
GO:0048566 embryonic digestive tract development
GO:0048589 developmental growth
GO:0048666 neuron development
GO:0048754 branching morphogenesis of an epithelial tube
Cellular Component
GO:0005634 nucleus
Protein Structure and Domains
PDB ID
InterPro IPR007087 Zinc finger, C2H2
IPR015880 Zinc finger, C2H2-like
PFAM PF00096
PRINTS
PIRSF
SMART SM00355
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt P10070
PhosphoSite PhosphoSite-P10070
TrEMBL Q6RSW2
UniProt Splice Variant
Entrez Gene 2736
UniGene Hs.111867
RefSeq NP_005261
HUGO HGNC:4318
OMIM 165230
CCDS CCDS33283
HPRD 01312
IMGT
EMBL AB007295 AB007296 AB007297 AB007298 AB209354 AC016764 AC017033 AY493737 D14827 D14828 DQ004397 DQ004398 DQ086814 M20672 M20673
GenPept AAA35898 AAS72889 AAY58316 AAY58317 AAY87165 BAA03568 BAA03569 BAA25665 BAA25666 BAA25667 BAA25668 BAD92591