| Nomenclature |
HGNC (Hugo) | LHX4 21734 |
| Cards |
Entrez_Gene (NCBI) | LHX4 LIM homeobox 4 |
Aliases | CPHD4 |
GeneCards (Weizmann) | LHX4 |
Ensembl hg19 (Hinxton) | ENSG00000121454 [Gene_View] |
Ensembl hg38 (Hinxton) | ENSG00000121454 [Gene_View]  ENSG00000121454 [Sequence] chr1:180230264-180278984 [Contig_View] LHX4 [Vega] |
ICGC DataPortal | ENSG00000121454 |
TCGA cBioPortal | LHX4 |
AceView (NCBI) | LHX4 |
Genatlas (Paris) | LHX4 |
SOURCE (Princeton) | LHX4 |
Genetics Home Reference (NIH) | LHX4 |
| Genomic and cartography |
GoldenPath hg38 (UCSC) | LHX4 - chr1:180230264-180278984 + 1q25.2 [Description] (hg38-Dec_2013) |
GoldenPath hg19 (UCSC) | LHX4 - 1q25.2 [Description] (hg19-Feb_2009) |
GoldenPath | LHX4 - 1q25.2 [CytoView hg19] LHX4 - 1q25.2 [CytoView hg38] |
ImmunoBase | ENSG00000121454 |
genome Data Viewer NCBI | LHX4 [Mapview hg19] |
OMIM | 262700 602146 |
| Gene and transcription |
Genbank (Entrez) | AB037683 AB055703 AB055704 AF179849 AF282899 |
RefSeq transcript (Entrez) | NM_033343 |
RefSeq genomic (Entrez) | |
Consensus coding sequences : CCDS (NCBI) | LHX4 |
Alternative Splicing Gallery | ENSG00000121454 |
Gene Expression | LHX4 [ NCBI-GEO ] LHX4 [ EBI - ARRAY_EXPRESS ]
LHX4 [ SEEK ] LHX4 [ MEM ] |
Gene Expression Viewer (FireBrowse) | LHX4 [ Firebrowse - Broad ] |
Genevisible | Expression of LHX4 in : [tissues]  [cell-lines]  [cancer]  [perturbations]   |
BioGPS (Tissue expression) | 89884 |
GTEX Portal (Tissue expression) | LHX4 |
Human Protein Atlas | ENSG00000121454-LHX4 [pathology] [cell] [tissue] |
| Protein : pattern, domain, 3D structure |
UniProt/SwissProt | Q969G2 [function] [subcellular_location] [family_and_domains] [pathology_and_biotech] [ptm_processing] [expression] [interaction] |
NextProt | Q969G2 [Sequence] [Exons] [Medical] [Publications] |
With graphics : InterPro | Q969G2 |
Splice isoforms : SwissVar | Q969G2 |
PhosPhoSitePlus | Q969G2 |
Domaine pattern : Prosite (Expaxy) | HOMEOBOX_1 (PS00027) HOMEOBOX_2 (PS50071) LIM_DOMAIN_1 (PS00478) LIM_DOMAIN_2 (PS50023) |
Domains : Interpro (EBI) | Homeobox-like_sf Homeobox_CS Homeobox_dom Znf_LIM |
Domain families : Pfam (Sanger) | Homeodomain (PF00046) LIM (PF00412) |
Domain families : Pfam (NCBI) | pfam00046 pfam00412 |
Domain families : Smart (EMBL) | HOX (SM00389) LIM (SM00132) |
Conserved Domain (NCBI) | LHX4 |
Blocks (Seattle) | LHX4 |
PDB (RSDB) | 5HOD |
PDB Europe | 5HOD |
PDB (PDBSum) | 5HOD |
PDB (IMB) | 5HOD |
Structural Biology KnowledgeBase | 5HOD |
SCOP (Structural Classification of Proteins) | 5HOD |
CATH (Classification of proteins structures) | 5HOD |
Superfamily | Q969G2 |
Human Protein Atlas [tissue] | ENSG00000121454-LHX4 [tissue] |
Peptide Atlas | Q969G2 |
HPRD | 03686 |
IPI | IPI00169275 |
| Protein Interaction databases |
DIP (DOE-UCLA) | Q969G2 |
IntAct (EBI) | Q969G2 |
BioGRID | LHX4 |
STRING (EMBL) | LHX4 |
ZODIAC | LHX4 |
| Ontologies - Pathways |
QuickGO | Q969G2 |
Ontology : AmiGO | chromatin RNA polymerase II transcription regulatory region sequence-specific DNA binding DNA-binding transcription factor activity, RNA polymerase II-specific DNA-binding transcription factor activity, RNA polymerase II-specific DNA-binding transcription activator activity, RNA polymerase II-specific placenta development protein binding nucleus regulation of transcription by RNA polymerase II motor neuron axon guidance methyl-CpG binding animal organ morphogenesis medial motor column neuron differentiation neuron differentiation negative regulation of apoptotic process sequence-specific DNA binding positive regulation of transcription by RNA polymerase II metal ion binding sequence-specific double-stranded DNA binding |
Ontology : EGO-EBI | chromatin RNA polymerase II transcription regulatory region sequence-specific DNA binding DNA-binding transcription factor activity, RNA polymerase II-specific DNA-binding transcription factor activity, RNA polymerase II-specific DNA-binding transcription activator activity, RNA polymerase II-specific placenta development protein binding nucleus regulation of transcription by RNA polymerase II motor neuron axon guidance methyl-CpG binding animal organ morphogenesis medial motor column neuron differentiation neuron differentiation negative regulation of apoptotic process sequence-specific DNA binding positive regulation of transcription by RNA polymerase II metal ion binding sequence-specific double-stranded DNA binding |
NDEx Network | LHX4 |
Atlas of Cancer Signalling Network | LHX4 |
Wikipedia pathways | LHX4 |
| Orthology - Evolution |
OrthoDB | 89884 |
GeneTree (enSembl) | ENSG00000121454 |
Phylogenetic Trees/Animal Genes : TreeFam | LHX4 |
HOGENOM | Q969G2 |
Homologs : HomoloGene | LHX4 |
Homology/Alignments : Family Browser (UCSC) | LHX4 |
| Gene fusions - Rearrangements |
Fusion : Mitelman | CCT8/LHX4 [21q21.3/1q25.2]   |
Fusion : Mitelman | IGH/LHX4 [14q32.33/1q25.2]   |
Fusion Portal | CCT8 21q21.3 LHX4 1q25.2 BRCA |
Fusion : Quiver | LHX4 |
| Polymorphisms : SNP and Copy number variants |
NCBI Variation Viewer | LHX4 [hg38] |
dbVar | LHX4 |
ClinVar | LHX4 |
Monarch | LHX4 |
1000_Genomes | LHX4 |
Exome Variant Server | LHX4 |
GNOMAD Browser | ENSG00000121454 |
Varsome Browser | LHX4 |
Genomic Variants (DGV) | LHX4 [DGVbeta] |
DECIPHER | LHX4 [patients] [syndromes] [variants] [genes] |
CONAN: Copy Number Analysis | LHX4 |
| Mutations |
ICGC Data Portal | LHX4 |
TCGA Data Portal | LHX4 |
Broad Tumor Portal | LHX4 |
OASIS Portal | LHX4 [ Somatic mutations - Copy number] |
Somatic Mutations in Cancer : COSMIC | LHX4 [overview] [genome browser] [tissue] [distribution] |
Somatic Mutations in Cancer : COSMIC3D | LHX4 |
Mutations and Diseases : HGMD | LHX4 |
LOVD (Leiden Open Variation Database) | Whole genome datasets |
LOVD (Leiden Open Variation Database) | LOVD - Leiden Open Variation Database |
LOVD (Leiden Open Variation Database) | LOVD 3.0 shared installation |
BioMuta | search LHX4 |
DgiDB (Drug Gene Interaction Database) | LHX4 |
DoCM (Curated mutations) | LHX4 (select the gene name) |
CIViC (Clinical Interpretations of Variants in Cancer) | LHX4 (select a term) |
intoGen | LHX4 |
Cancer3D | LHX4(select the gene name) |
Impact of mutations | [PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser] |
| Diseases |
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OMIM | 262700 602146 |
Orphanet | 19033 11716 12620 12618 |
DisGeNET | LHX4 |
Medgen | LHX4 |
Genetic Testing Registry | LHX4
|
NextProt | Q969G2 [Medical] |
GENETests | LHX4 |
Target Validation | LHX4 |
Huge Navigator |
LHX4 [HugePedia] |
ClinGen | LHX4 (curated) |
| Clinical trials, drugs, therapy |
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MyCancerGenome | LHX4 |
Protein Interactions : CTD | |
Pharm GKB Gene | PA134962876 |
Pharos | Q969G2 |
Clinical trial | LHX4 |
| Miscellaneous |
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canSAR (ICR) | LHX4 (select the gene name) |
Harmonizome | LHX4 |
DataMed Index | LHX4 |
| Probes |
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| Litterature |
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PubMed | 40 Pubmed reference(s) in Entrez |
GeneRIFs | Gene References Into Functions (Entrez) |
EVEX | LHX4 |