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: 9419
MIM: 604594
HGNC: 14312
Ensembl: ENSG00000119878
Variants:
dbSNP: 9419
ClinVar: 9419
TCGA: ENSG00000119878
COSMIC: CRIPT
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000119878 | ENST00000238892 | Q9P021 |
Expression (GTEx)
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 37013901 | 2023 | Biallelic variants in CRIPT cause a Rothmund-Thomson-like syndrome with increased cellular senescence. | 3 |
| 37013901 | 2023 | Biallelic variants in CRIPT cause a Rothmund-Thomson-like syndrome with increased cellular senescence. | 3 |
| 36148798 | 2022 | Mitotic spindle disassembly in human cells relies on CRIPT having hierarchical redox signals. | 0 |
| 36148798 | 2022 | Mitotic spindle disassembly in human cells relies on CRIPT having hierarchical redox signals. | 0 |
| 32750125 | 2021 | Divergent Evolution of a Protein-Protein Interaction Revealed through Ancestral Sequence Reconstruction and Resurrection. | 5 |
| 32750125 | 2021 | Divergent Evolution of a Protein-Protein Interaction Revealed through Ancestral Sequence Reconstruction and Resurrection. | 5 |
| 30864948 | 2019 | Intramolecular domain dynamics regulate synaptic MAGUK protein interactions. | 23 |
| 30864948 | 2019 | Intramolecular domain dynamics regulate synaptic MAGUK protein interactions. | 23 |
| 27250922 | 2016 | CRIPT exonic deletion and a novel missense mutation in a female with short stature, dysmorphic features, microcephaly, and pigmentary abnormalities. | 8 |
| 27250922 | 2016 | CRIPT exonic deletion and a novel missense mutation in a female with short stature, dysmorphic features, microcephaly, and pigmentary abnormalities. | 8 |
| 20398908 | 2010 | Comprehensive copy number variant (CNV) analysis of neuronal pathways genes in psychiatric disorders identifies rare variants within patients. | 34 |
| 20398908 | 2010 | Comprehensive copy number variant (CNV) analysis of neuronal pathways genes in psychiatric disorders identifies rare variants within patients. | 34 |
| 19086053 | 2009 | Identification of new putative susceptibility genes for several psychiatric disorders by association analysis of regulatory and non-synonymous SNPs of 306 genes involved in neurotransmission and neurodevelopment. | 39 |
| 19086053 | 2009 | Identification of new putative susceptibility genes for several psychiatric disorders by association analysis of regulatory and non-synonymous SNPs of 306 genes involved in neurotransmission and neurodevelopment. | 39 |
Citation
Dessen P
CRIPT (CXXC repeat containing interactor of PDZ3 domain)
Atlas Genet Cytogenet Oncol Haematol. 2014-11-01
Online version: http://atlasgeneticsoncology.org/gene/62088/cript-(cxxc-repeat-containing-interactor-of-pdz3-domain)
