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: 8675
MIM: 603666
HGNC: 11431
Ensembl: ENSG00000124222
Variants:
dbSNP: 8675
ClinVar: 8675
TCGA: ENSG00000124222
COSMIC: STX16
RNA/Proteins
Expression (GTEx)
Pathways
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 38095637 | 2024 | Intrafamilial phenotypic heterogeneity in siblings with pseudohypoparathyroidism 1B due to maternal STX16 deletion. | 0 |
| 38095637 | 2024 | Intrafamilial phenotypic heterogeneity in siblings with pseudohypoparathyroidism 1B due to maternal STX16 deletion. | 0 |
| 33269569 | 2022 | Analysis of defects in GNAS and STX16 genes in a Chinese family with pseudohypoparathyroidism. | 1 |
| 34477200 | 2022 | Progression of PTH Resistance in Autosomal Dominant Pseudohypoparathyroidism Type Ib Due to Maternal STX16 Deletions. | 5 |
| 33269569 | 2022 | Analysis of defects in GNAS and STX16 genes in a Chinese family with pseudohypoparathyroidism. | 1 |
| 34477200 | 2022 | Progression of PTH Resistance in Autosomal Dominant Pseudohypoparathyroidism Type Ib Due to Maternal STX16 Deletions. | 5 |
| 33247854 | 2021 | Preferential Maternal Transmission of STX16-GNAS Mutations Responsible for Autosomal Dominant Pseudohypoparathyroidism Type Ib (PHP1B): Another Example of Transmission Ratio Distortion. | 4 |
| 33247854 | 2021 | Preferential Maternal Transmission of STX16-GNAS Mutations Responsible for Autosomal Dominant Pseudohypoparathyroidism Type Ib (PHP1B): Another Example of Transmission Ratio Distortion. | 4 |
| 27338644 | 2016 | Macrosomia, obesity, and macrocephaly as first clinical presentation of PHP1b caused by STX16 deletion. | 10 |
| 27338644 | 2016 | Macrosomia, obesity, and macrocephaly as first clinical presentation of PHP1b caused by STX16 deletion. | 10 |
| 25843330 | 2015 | Growth hormone deficiency in monozygotic twins with autosomal dominant pseudohypoparathyroidism type Ib. | 5 |
| 25843330 | 2015 | Growth hormone deficiency in monozygotic twins with autosomal dominant pseudohypoparathyroidism type Ib. | 5 |
| 23095209 | 2013 | Neuromuscular symptoms in a patient with familial pseudohypoparathyroidism type Ib diagnosed by methylation-specific multiplex ligation-dependent probe amplification. | 6 |
| 23677696 | 2013 | VAMP4 is required to maintain the ribbon structure of the Golgi apparatus. | 17 |
| 24109596 | 2013 | Syntaxin 16 is a master recruitment factor for cytokinesis. | 20 |
Citation
Dessen P
STX16 (syntaxin 16)
Atlas Genet Cytogenet Oncol Haematol. 2014-08-01
Online version: http://atlasgeneticsoncology.org/gene/54674/stx16-(syntaxin-16)
