TBX15 - T-box transcription factor 15 Gene
Also Known as TBX14
Species: Homo sapiens
About TBX15
This gene has 3 transcripts (splice variants), 233 orthologues, 16 paralogues and is associated with 3 phenotypes. Biased expression in fat (RPKM 11.5), liver (RPKM 10.7) and 4 other tissues.
Summary
This gene belongs to the T-box family of genes, which encode a phylogenetically conserved family of transcription factors that regulate a variety of developmental processes. All these genes contain a common T-box DNA-binding domain. Mutations in this gene are associated with Cousin syndrome.[provided by RefSeq, Oct 2009]
TBX15 Products (2)
| mRNA | Protein | Name |
|---|---|---|
| NM_001330677.2 | NP_001317606.1 | T-box transcription factor TBX15 isoform 1 |
| NM_152380.3 | NP_689593.2 | T-box transcription factor TBX15 isoform 2 |
| Molecular Function GO Annotation | Evidence | Références | Source |
|---|---|---|---|
| enables protein binding |
IPI
IPI: Inferred from physical interaction
|
25416956 | GOA |
| enables sequence-specific double-stranded DNA binding |
IDA
IDA: Inferred from direct assay
|
28473536 | GOA |
TBX15 Protein Structure
T-box: T-box (114 - 305)
- 0
- 100
- 200
- 300
- 400
- 500
- 602 a.a.
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
T-box transcription factor TBX15 |
|
TBX15 Protein-protein interaction Information
|
Type
|
Protein Name | Protein ID | Interactor | Interactor Species | Interactor ID | Detection Method | Références |
|---|---|---|---|---|---|---|---|
|
Intra
|
TBX15 | Q96SF7 | VENTX | Homo sapiens | O95231 | 25416956 | |
|
Intra
|
TBX15 | Q96SF7 | VENTX | Homo sapiens | O95231 | 31515488 | |
|
Intra
|
TBX15 | Q96SF7 | POLE2 | Homo sapiens | P56282 | 25416956 | |
|
Intra
|
TBX15 | Q96SF7 | ATXN1 | Homo sapiens | P54253 | 25416956 | |
|
Intra
|
TBX15 | Q96SF7 | ATXN1 | Homo sapiens | P54253 | 25416956 |
Related Diseases
| Diseases | Alias | |
|---|---|---|
| Cousin Syndrome |
|
|
| Acromegaloid Facial Appearance Syndrome |
|
|
| Ulnar-Mammary Syndrome |
|
|
| Cleft Palate With Or Without Ankyloglossia, X-Linked |
|
|
| Robinow Syndrome, Autosomal Recessive 1 |
|
|
| Strabismus |
|
|
| Brachydactyly |
|
Orthologs Information
| Species | Symbol | Source | ID |
|---|---|---|---|
| Bos taurus | TBX15 | VGNC | VGNC:55686 |
| Felis catus | TBX15 | VGNC | VGNC:107673 |
| Macaca mulatta | TBX15 | VGNC | VGNC:78268 |
| Mus musculus | TBX15 | MGD | MGI:1277234 |
| Rattus norvegicus | TBX15 | RGD | RGD:1308094 |
| Canis familiaris | TBX15 | VGNC | VGNC:47169 |
| Others | TBX15 | NCBI |