Identity
HGNC
LOCATION
3q12.1
LOCUSID
ALIAS
NS4ATP1,PCH11
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: 55773
MIM: 617687
HGNC: 25622
Ensembl: ENSG00000036054
Variants:
dbSNP: 55773
ClinVar: 55773
TCGA: ENSG00000036054
COSMIC: TBC1D23
RNA/Proteins
Expression (GTEx)
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 37903274 | 2023 | FAM91A1-TBC1D23 complex structure reveals human genetic variations susceptible for PCH. | 3 |
| 37903274 | 2023 | FAM91A1-TBC1D23 complex structure reveals human genetic variations susceptible for PCH. | 3 |
| 34363324 | 2021 | TBC1 domain family member 23 interacts with Ras-related protein Rab-11A to promote poor prognosis of non-small-cell lung cancer via β1-integrin. | 3 |
| 34363324 | 2021 | TBC1 domain family member 23 interacts with Ras-related protein Rab-11A to promote poor prognosis of non-small-cell lung cancer via β1-integrin. | 3 |
| 32453802 | 2020 | Structure of TBC1D23 N-terminus reveals a novel role for rhodanese domain. | 11 |
| 32453802 | 2020 | Structure of TBC1D23 N-terminus reveals a novel role for rhodanese domain. | 11 |
| 31624125 | 2019 | Structural and functional studies of TBC1D23 C-terminal domain provide a link between endosomal trafficking and PCH. | 18 |
| 31624125 | 2019 | Structural and functional studies of TBC1D23 C-terminal domain provide a link between endosomal trafficking and PCH. | 18 |
| 28823706 | 2017 | Homozygous Mutations in TBC1D23 Lead to a Non-degenerative Form of Pontocerebellar Hypoplasia. | 26 |
| 28823707 | 2017 | Homozygous Truncating Variants in TBC1D23 Cause Pontocerebellar Hypoplasia and Alter Cortical Development. | 27 |
| 29084197 | 2017 | TBC1D23 is a bridging factor for endosomal vesicle capture by golgins at the trans-Golgi. | 35 |
| 28823706 | 2017 | Homozygous Mutations in TBC1D23 Lead to a Non-degenerative Form of Pontocerebellar Hypoplasia. | 26 |
| 28823707 | 2017 | Homozygous Truncating Variants in TBC1D23 Cause Pontocerebellar Hypoplasia and Alter Cortical Development. | 27 |
| 29084197 | 2017 | TBC1D23 is a bridging factor for endosomal vesicle capture by golgins at the trans-Golgi. | 35 |
Citation
Dessen P
TBC1D23 (TBC1 domain family member 23)
Atlas Genet Cytogenet Oncol Haematol. 2003-12-01
Online version: http://atlasgeneticsoncology.org/gene/40590/tbc1d23
