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: 84189
MIM: 609681
HGNC: 23503
Ensembl: ENSG00000184564
Variants:
dbSNP: 84189
ClinVar: 84189
TCGA: ENSG00000184564
COSMIC: SLITRK6
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000184564 | ENST00000643778 | Q9H5Y7 |
| ENSG00000184564 | ENST00000647374 | Q9H5Y7 |
Expression (GTEx)
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 37219677 | 2023 | SLITRK6 promotes the progression of lung adenocarcinoma by regulating PI3K/AKT/mTOR signaling and Warburg effect. | 2 |
| 37353040 | 2023 | Differential expression of SLITRK6 gene as a potential therapeutic target for urothelial carcinoma in particular upper tract cancer. | 2 |
| 37219677 | 2023 | SLITRK6 promotes the progression of lung adenocarcinoma by regulating PI3K/AKT/mTOR signaling and Warburg effect. | 2 |
| 37353040 | 2023 | Differential expression of SLITRK6 gene as a potential therapeutic target for urothelial carcinoma in particular upper tract cancer. | 2 |
| 32037697 | 2020 | The role of SLITRK6 in the pathogenesis of Tourette syndrome: From the conclusion of a family-based study in the Chinese Han population. | 2 |
| 32037697 | 2020 | The role of SLITRK6 in the pathogenesis of Tourette syndrome: From the conclusion of a family-based study in the Chinese Han population. | 2 |
| 29551497 | 2018 | A novel mutation in SLITRK6 causes deafness and myopia in a Moroccan family. | 2 |
| 29551497 | 2018 | A novel mutation in SLITRK6 causes deafness and myopia in a Moroccan family. | 2 |
| 27530937 | 2017 | Human cytomegalovirus downregulates SLITRK6 expression through IE2. | 1 |
| 27530937 | 2017 | Human cytomegalovirus downregulates SLITRK6 expression through IE2. | 1 |
| 23946138 | 2014 | A homozygous SLITRK6 nonsense mutation is associated with progressive auditory neuropathy in humans. | 5 |
| 23946138 | 2014 | A homozygous SLITRK6 nonsense mutation is associated with progressive auditory neuropathy in humans. | 5 |
| 23543054 | 2013 | SLITRK6 mutations cause myopia and deafness in humans and mice. | 30 |
| 23543054 | 2013 | SLITRK6 mutations cause myopia and deafness in humans and mice. | 30 |
Citation
Dessen P
SLITRK6 (SLIT and NTRK like family member 6)
Atlas Genet Cytogenet Oncol Haematol. 2014-11-01
Online version: http://atlasgeneticsoncology.org/gene/73524/slitrk6-(slit-and-ntrk-like-family-member-6)
