| Nomenclature |
HGNC (Hugo) | TBX15 11594 |
| Cards |
Entrez_Gene (NCBI) | TBX15 6913 T-box transcription factor 15 |
Aliases | TBX14 |
GeneCards (Weizmann) | TBX15 |
Ensembl hg19 (Hinxton) | ENSG00000092607 [Gene_View] |
Ensembl hg38 (Hinxton) | ENSG00000092607 [Gene_View]  ENSG00000092607 [Sequence] chr1:118883043-118989556 [Contig_View] TBX15 [Vega] |
ICGC DataPortal | ENSG00000092607 |
TCGA cBioPortal | TBX15 |
AceView (NCBI) | TBX15 |
Genatlas (Paris) | TBX15 |
WikiGenes | 6913 |
SOURCE (Princeton) | TBX15 |
Genetics Home Reference (NIH) | TBX15 |
| Genomic and cartography |
GoldenPath hg38 (UCSC) | TBX15 - chr1:118883043-118989556 - 1p12 [Description] (hg38-Dec_2013) |
GoldenPath hg19 (UCSC) | TBX15 - 1p12 [Description] (hg19-Feb_2009) |
GoldenPath | TBX15 - 1p12 [CytoView hg19] TBX15 - 1p12 [CytoView hg38] |
ImmunoBase | ENSG00000092607 |
Mapping of homologs : NCBI | TBX15 [Mapview hg19] TBX15 [Mapview hg38] |
OMIM | 260660 604127 |
| Gene and transcription |
Genbank (Entrez) | AK096396 AK127536 BC122553 BX537778 CA412451 |
RefSeq transcript (Entrez) | NM_001330677 NM_152380 |
RefSeq genomic (Entrez) | |
Consensus coding sequences : CCDS (NCBI) | TBX15 |
Cluster EST : Unigene | Hs.146196 [ NCBI ] |
CGAP (NCI) | Hs.146196 |
Alternative Splicing Gallery | ENSG00000092607 |
Gene Expression | TBX15 [ NCBI-GEO ] TBX15 [ EBI - ARRAY_EXPRESS ]
TBX15 [ SEEK ] TBX15 [ MEM ] |
Gene Expression Viewer (FireBrowse) | TBX15 [ Firebrowse - Broad ] |
SOURCE (Princeton) | Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60] |
Genevestigator | Expression in : [tissues]  [cell-lines]  [cancer]  [perturbations]   |
BioGPS (Tissue expression) | 6913 |
GTEX Portal (Tissue expression) | TBX15 |
Human Protein Atlas | ENSG00000092607-TBX15 [pathology] [cell] [tissue] |
| Protein : pattern, domain, 3D structure |
UniProt/SwissProt | Q96SF7 [function] [subcellular_location] [family_and_domains] [pathology_and_biotech] [ptm_processing] [expression] [interaction] |
NextProt | Q96SF7 [Sequence] [Exons] [Medical] [Publications] |
With graphics : InterPro | Q96SF7 |
Splice isoforms : SwissVar | Q96SF7 |
PhosPhoSitePlus | Q96SF7 |
Domaine pattern : Prosite (Expaxy) | TBOX_1 (PS01283) TBOX_2 (PS01264) TBOX_3 (PS50252) |
Domains : Interpro (EBI) | p53-like_TF_DNA-bd T-box_sf TF_T-box TF_T-box_CS |
Domain families : Pfam (Sanger) | T-box (PF00907) |
Domain families : Pfam (NCBI) | pfam00907 |
Domain families : Smart (EMBL) | TBOX (SM00425) |
Conserved Domain (NCBI) | TBX15 |
DMDM Disease mutations | 6913 |
Blocks (Seattle) | TBX15 |
Superfamily | Q96SF7 |
Human Protein Atlas [tissue] | ENSG00000092607-TBX15 [tissue] |
Peptide Atlas | Q96SF7 |
HPRD | 16035 |
IPI | IPI00163361 IPI00643004 IPI00844280 IPI00874142 |
| Protein Interaction databases |
DIP (DOE-UCLA) | Q96SF7 |
IntAct (EBI) | Q96SF7 |
FunCoup | ENSG00000092607 |
BioGRID | TBX15 |
STRING (EMBL) | TBX15 |
ZODIAC | TBX15 |
| Ontologies - Pathways |
QuickGO | Q96SF7 |
Ontology : AmiGO | negative regulation of transcription by RNA polymerase II negative regulation of transcription by RNA polymerase II RNA polymerase II regulatory region sequence-specific DNA binding RNA polymerase II proximal promoter sequence-specific DNA binding DNA-binding transcription factor activity, RNA polymerase II-specific DNA-binding transcription factor activity, RNA polymerase II-specific RNA polymerase II activating transcription factor binding DNA-binding transcription repressor activity, RNA polymerase II-specific DNA-binding transcription activator activity, RNA polymerase II-specific cell fate specification protein binding nucleus protein homodimerization activity positive regulation of transcription by RNA polymerase II protein heterodimerization activity embryonic cranial skeleton morphogenesis Tle3-Aes complex Tle3-Aes complex |
Ontology : EGO-EBI | negative regulation of transcription by RNA polymerase II negative regulation of transcription by RNA polymerase II RNA polymerase II regulatory region sequence-specific DNA binding RNA polymerase II proximal promoter sequence-specific DNA binding DNA-binding transcription factor activity, RNA polymerase II-specific DNA-binding transcription factor activity, RNA polymerase II-specific RNA polymerase II activating transcription factor binding DNA-binding transcription repressor activity, RNA polymerase II-specific DNA-binding transcription activator activity, RNA polymerase II-specific cell fate specification protein binding nucleus protein homodimerization activity positive regulation of transcription by RNA polymerase II protein heterodimerization activity embryonic cranial skeleton morphogenesis Tle3-Aes complex Tle3-Aes complex |
NDEx Network | TBX15 |
Atlas of Cancer Signalling Network | TBX15 |
Wikipedia pathways | TBX15 |
| Orthology - Evolution |
OrthoDB | 6913 |
GeneTree (enSembl) | ENSG00000092607 |
Phylogenetic Trees/Animal Genes : TreeFam | TBX15 |
HOGENOM | Q96SF7 |
Homologs : HomoloGene | TBX15 |
Homology/Alignments : Family Browser (UCSC) | TBX15 |
| Gene fusions - Rearrangements |
Fusion : Mitelman | DDX20/TBX15 [1p13.2/1p12]  [t(1;1)(p12;p13)] |
Fusion : Mitelman | IGSF3/TBX15 [1p13.1/1p12]  [t(1;1)(p12;p13)] |
Fusion Portal | DDX20 1p13.2 TBX15 1p12 LAML |
Fusion Portal | IGSF3 1p13.1 TBX15 1p12 BRCA |
Fusion : Quiver | TBX15 |
| Polymorphisms : SNP and Copy number variants |
NCBI Variation Viewer | TBX15 [hg38] |
dbSNP Single Nucleotide Polymorphism (NCBI) | TBX15 |
dbVar | TBX15 |
ClinVar | TBX15 |
1000_Genomes | TBX15 |
Exome Variant Server | TBX15 |
ExAC (Exome Aggregation Consortium) | ENSG00000092607 |
GNOMAD Browser | ENSG00000092607 |
Varsome Browser | TBX15 |
Genetic variants : HAPMAP | 6913 |
Genomic Variants (DGV) | TBX15 [DGVbeta] |
DECIPHER | TBX15 [patients] [syndromes] [variants] [genes] |
CONAN: Copy Number Analysis | TBX15 |
| Mutations |
ICGC Data Portal | TBX15 |
TCGA Data Portal | TBX15 |
Broad Tumor Portal | TBX15 |
OASIS Portal | TBX15 [ Somatic mutations - Copy number] |
Somatic Mutations in Cancer : COSMIC | TBX15 [overview] [genome browser] [tissue] [distribution] |
Somatic Mutations in Cancer : COSMIC3D | TBX15 |
Mutations and Diseases : HGMD | TBX15 |
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 TBX15 |
DgiDB (Drug Gene Interaction Database) | TBX15 |
DoCM (Curated mutations) | TBX15 (select the gene name) |
CIViC (Clinical Interpretations of Variants in Cancer) | TBX15 (select a term) |
intoGen | TBX15 |
Cancer3D | TBX15(select the gene name) |
Impact of mutations | [PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser] |
| Diseases |
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OMIM | 260660 604127 |
Orphanet | 12268 |
DisGeNET | TBX15 |
Medgen | TBX15 |
Genetic Testing Registry | TBX15
|
NextProt | Q96SF7 [Medical] |
TSGene | 6913 |
GENETests | TBX15 |
Target Validation | TBX15 |
Huge Navigator |
TBX15 [HugePedia] |
snp3D : Map Gene to Disease | 6913 |
BioCentury BCIQ | TBX15 |
ClinGen | TBX15 |
| Clinical trials, drugs, therapy |
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Chemical/Protein Interactions : CTD | 6913 |
Chemical/Pharm GKB Gene | PA36357 |
Clinical trial | TBX15 |
| Miscellaneous |
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canSAR (ICR) | TBX15 (select the gene name) |
DataMed Index | TBX15 |
| Probes |
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| Litterature |
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PubMed | 20 Pubmed reference(s) in Entrez |
GeneRIFs | Gene References Into Functions (Entrez) |
CoreMine | TBX15 |
EVEX | TBX15 |
GoPubMed | TBX15 |
iHOP | TBX15 |