Identity
HGNC
LOCATION
8q24.3
LOCUSID
ALIAS
IBP,IKBKBBP,MRT13,NIBP,T1,TRS120
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: 83696
MIM: 611966
HGNC: 30832
Ensembl: ENSG00000167632
Variants:
dbSNP: 83696
ClinVar: 83696
TCGA: ENSG00000167632
COSMIC: TRAPPC9
RNA/Proteins
Expression (GTEx)
Pathways
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 38467738 | 2024 | Expanding the genetic and phenotypic spectrum of TRAPPC9 and MID2-related neurodevelopmental disabilities: report of two novel mutations, 3D-modelling, and molecular docking studies. | 0 |
| 38467738 | 2024 | Expanding the genetic and phenotypic spectrum of TRAPPC9 and MID2-related neurodevelopmental disabilities: report of two novel mutations, 3D-modelling, and molecular docking studies. | 0 |
| 35760056 | 2022 | Neurodevelopmental Outcome and Epigenetic Changes at 2 Years Associated with the Oxygen Load Received upon Postnatal Stabilization: A Pilot Study. | 1 |
| 35760056 | 2022 | Neurodevelopmental Outcome and Epigenetic Changes at 2 Years Associated with the Oxygen Load Received upon Postnatal Stabilization: A Pilot Study. | 1 |
| 33513295 | 2021 | Identification of two novel homozygous nonsense mutations in TRAPPC9 in two unrelated consanguineous families with intellectual Disability from Iran. | 3 |
| 33921338 | 2021 | Novel Compound Heterozygous Mutation in TRAPPC9 Gene: The Relevance of Whole Genome Sequencing. | 9 |
| 34737153 | 2021 | Further insights into the spectrum phenotype of TRAPPC9 and CDK5RAP2 genes, segregating independently in a large Tunisian family with intellectual disability and microcephaly. | 2 |
| 33513295 | 2021 | Identification of two novel homozygous nonsense mutations in TRAPPC9 in two unrelated consanguineous families with intellectual Disability from Iran. | 3 |
| 33921338 | 2021 | Novel Compound Heterozygous Mutation in TRAPPC9 Gene: The Relevance of Whole Genome Sequencing. | 9 |
| 34737153 | 2021 | Further insights into the spectrum phenotype of TRAPPC9 and CDK5RAP2 genes, segregating independently in a large Tunisian family with intellectual disability and microcephaly. | 2 |
| 32046534 | 2020 | Contribution of Intellectual Disability-Related Genes to ADHD Risk and to Locomotor Activity in Drosophila. | 13 |
| 32877400 | 2020 | Trappc9 deficiency causes parent-of-origin dependent microcephaly and obesity. | 10 |
| 32046534 | 2020 | Contribution of Intellectual Disability-Related Genes to ADHD Risk and to Locomotor Activity in Drosophila. | 13 |
| 32877400 | 2020 | Trappc9 deficiency causes parent-of-origin dependent microcephaly and obesity. | 10 |
| 29187737 | 2018 | The role of CNVs in the etiology of rare autosomal recessive disorders: the example of TRAPPC9-associated intellectual disability. | 14 |
Citation
Dessen P
TRAPPC9 (trafficking protein particle complex subunit 9)
Atlas Genet Cytogenet Oncol Haematol. 2007-04-01
Online version: http://atlasgeneticsoncology.org/gene/47452/trappc9-(trafficking-protein-particle-complex-subunit-9)
