Identity
HGNC
LOCATION
1q24.2
LOCUSID
ALIAS
TBS19,TPIT,dJ747L4.1
FUSION GENES
Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 9095
MIM: 604614
HGNC: 11596
Ensembl: ENSG00000143178
Variants:
dbSNP: 9095
ClinVar: 9095
TCGA: ENSG00000143178
COSMIC: TBX19
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000143178 | ENST00000367821 | O60806 |
| ENSG00000143178 | ENST00000431969 | H0Y5A7 |
| ENSG00000143178 | ENST00000441464 | H0Y4B1 |
Expression (GTEx)
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 37726450 | 2023 | Heterogeneity of TPIT expression in ACTH-secreting extra-pituitary neuroendocrine tumors (NETs) supports the existence of different cellular programs in pancreatic and pulmonary NETs. | 1 |
| 37726450 | 2023 | Heterogeneity of TPIT expression in ACTH-secreting extra-pituitary neuroendocrine tumors (NETs) supports the existence of different cellular programs in pancreatic and pulmonary NETs. | 1 |
| 35217793 | 2022 | T-box transcription factor 19 promotes hepatocellular carcinoma metastasis through upregulating EGFR and RAC1. | 8 |
| 35218667 | 2022 | TRIM65 determines the fate of a novel subtype of pituitary neuroendocrine tumors via ubiquitination and degradation of TPIT. | 4 |
| 36890856 | 2022 | A novel TBX19 gene mutation in patients with isolated ACTH deficiency from distinct families with a common geographical origin. | 0 |
| 35217793 | 2022 | T-box transcription factor 19 promotes hepatocellular carcinoma metastasis through upregulating EGFR and RAC1. | 8 |
| 35218667 | 2022 | TRIM65 determines the fate of a novel subtype of pituitary neuroendocrine tumors via ubiquitination and degradation of TPIT. | 4 |
| 36890856 | 2022 | A novel TBX19 gene mutation in patients with isolated ACTH deficiency from distinct families with a common geographical origin. | 0 |
| 33423260 | 2021 | [Analysis of TBX19 gene variant in a child with congenital isolated adrenocorticotropic hormone deficiency]. | 1 |
| 33423260 | 2021 | [Analysis of TBX19 gene variant in a child with congenital isolated adrenocorticotropic hormone deficiency]. | 1 |
| 30747411 | 2019 | Evaluation of growth and puberty in a child with a novel TBX19 gene mutation and review of the literature. | 3 |
| 32344415 | 2019 | A Rare Cause of Adrenal Insufficiency - Isolated ACTH Deficiency Due to TBX19 Mutation: Long-Term Follow-Up of Two Cases and Review of the Literature. | 2 |
| 30747411 | 2019 | Evaluation of growth and puberty in a child with a novel TBX19 gene mutation and review of the literature. | 3 |
| 32344415 | 2019 | A Rare Cause of Adrenal Insufficiency - Isolated ACTH Deficiency Due to TBX19 Mutation: Long-Term Follow-Up of Two Cases and Review of the Literature. | 2 |
| 29199261 | 2017 | TBX19 is overexpressed in colorectal cancer and associated with lymph node metastasis. | 7 |
Citation
Dessen P
TBX19 (T-box transcription factor 19)
Atlas Genet Cytogenet Oncol Haematol. 2016-10-01
Online version: http://atlasgeneticsoncology.org/gene/56414/tbx19-(t-box-transcription-factor-19)
