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: 714
MIM: 120575
HGNC: 1245
Ensembl: ENSG00000159189
Variants:
dbSNP: 714
ClinVar: 714
TCGA: ENSG00000159189
COSMIC: C1QC
RNA/Proteins
Expression (GTEx)
Pathways
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 34320915 | 2022 | Neuroinflammation and psychiatric disorders: Relevance of C1q, translocator protein (18 kDa) (TSPO), and neurosteroids. | 8 |
| 35765947 | 2022 | Complement C1QC as a potential prognostic marker and therapeutic target in colon carcinoma based on single-cell RNA sequencing and immunohistochemical analysis. | 7 |
| 34320915 | 2022 | Neuroinflammation and psychiatric disorders: Relevance of C1q, translocator protein (18 kDa) (TSPO), and neurosteroids. | 8 |
| 35765947 | 2022 | Complement C1QC as a potential prognostic marker and therapeutic target in colon carcinoma based on single-cell RNA sequencing and immunohistochemical analysis. | 7 |
| 33131194 | 2021 | C1q-binding DSA and allograft outcomes in pediatric kidney transplant recipients. | 4 |
| 33131194 | 2021 | C1q-binding DSA and allograft outcomes in pediatric kidney transplant recipients. | 4 |
| 33182045 | 2020 | Clinical and prognostic significance of C1q deposition in IgAN patients-a retrospective study. | 2 |
| 33182045 | 2020 | Clinical and prognostic significance of C1q deposition in IgAN patients-a retrospective study. | 2 |
| 31019999 | 2019 | C1QA and C1QC modify age-at-onset in familial amyloid polyneuropathy patients. | 7 |
| 31019999 | 2019 | C1QA and C1QC modify age-at-onset in familial amyloid polyneuropathy patients. | 7 |
| 24157463 | 2014 | Rothmund-Thomson syndrome and glomerulonephritis in a homozygous C1q-deficient patient due to a Gly164Ser C1qC mutation. | 1 |
| 25109258 | 2014 | Complement activation in patients with neuromyelitis optica. | 32 |
| 24157463 | 2014 | Rothmund-Thomson syndrome and glomerulonephritis in a homozygous C1q-deficient patient due to a Gly164Ser C1qC mutation. | 1 |
| 25109258 | 2014 | Complement activation in patients with neuromyelitis optica. | 32 |
| 23607884 | 2013 | Genetic variants in the region of the C1q genes are associated with rheumatoid arthritis. | 17 |
Citation
Dessen P
C1QC (complement C1q C chain)
Atlas Genet Cytogenet Oncol Haematol. 2011-02-01
Online version: http://atlasgeneticsoncology.org/gene/52054/c1qc
