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: 114902
MIM: 608752
HGNC: 14344
Ensembl: ENSG00000223953
Variants:
dbSNP: 114902
ClinVar: 114902
TCGA: ENSG00000223953
COSMIC: C1QTNF5
RNA/Proteins
Expression (GTEx)
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 38246238 | 2024 | C1QTNF5 is a novel attachment factor that facilitates the entry of influenza A virus. | 0 |
| 38246238 | 2024 | C1QTNF5 is a novel attachment factor that facilitates the entry of influenza A virus. | 0 |
| 38085246 | 2023 | Longitudinal Changes of Retinal Structure in Molecularly Confirmed C1QTNF5 Patients With Late-Onset Retinal Degeneration. | 0 |
| 38085246 | 2023 | Longitudinal Changes of Retinal Structure in Molecularly Confirmed C1QTNF5 Patients With Late-Onset Retinal Degeneration. | 0 |
| 32202952 | 2022 | Evaluation of changing the pattern of CTRP5 and inflammatory markers levels in patients with coronary artery disease and type 2 diabetes mellitus. | 4 |
| 34907845 | 2022 | Increased serum myonectin and irisin levels with myonectin and FNDC5 expressions in polycystic ovary syndrome: a case control study. | 3 |
| 36457269 | 2022 | Upregulation of IL-8, osteonectin, and myonectin mRNAs by intermittent hypoxia via OCT1- and NRF2-mediated mechanisms in skeletal muscle cells. | 7 |
| 32202952 | 2022 | Evaluation of changing the pattern of CTRP5 and inflammatory markers levels in patients with coronary artery disease and type 2 diabetes mellitus. | 4 |
| 34907845 | 2022 | Increased serum myonectin and irisin levels with myonectin and FNDC5 expressions in polycystic ovary syndrome: a case control study. | 3 |
| 36457269 | 2022 | Upregulation of IL-8, osteonectin, and myonectin mRNAs by intermittent hypoxia via OCT1- and NRF2-mediated mechanisms in skeletal muscle cells. | 7 |
| 33669876 | 2021 | Autosomal Dominant Gyrate Atrophy-Like Choroidal Dystrophy Revisited: 45 Years Follow-Up and Association with a Novel C1QTNF5 Missense Variant. | 5 |
| 33785845 | 2021 | Association of serum and aqueous humor myonectin concentrations with diabetic retinopathy. | 2 |
| 33949280 | 2021 | Longitudinal phenotypic study of late-onset retinal degeneration due to a founder variant c.562C>A p.(Pro188Thr) in the C1QTNF5 gene. | 6 |
| 33990119 | 2021 | MASSIVE ADVANCING NONEXUDATIVE TYPE 1 CHOROIDAL NEOVASCULARIZATION IN CTRP5 LATE-ONSET RETINAL DEGENERATION: Longitudinal Findings on Multimodal Imaging and Implications for Age-Related Macular Degeneration. | 3 |
| 34887495 | 2021 | AMPK modulation ameliorates dominant disease phenotypes of CTRP5 variant in retinal degeneration. | 12 |
Citation
Dessen P
C1QTNF5 (C1q and TNF related 5)
Atlas Genet Cytogenet Oncol Haematol. 2003-06-01
Online version: http://atlasgeneticsoncology.org/gene/877/c1qtnf5
