C1QL1
C1q-related factor
Also known as: C1QRF, C1QRF_HUMAN, C1QTNF14, CRF, CTRP14
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O75973
- Gene
- C1QL1
- Ensembl
- ENSG00000131094
- Chromosome
- 17
- Canonical length
- 258 aa
- Protein class
- Plasma proteins, Predicted secreted proteins
- Subcellular location
- Vesicles,Cytosol
- Secretome location
- Secreted in brain
OverviewNCBI Gene
Predicted to enable signaling receptor binding activity. Predicted to be involved in locomotory behavior. Predicted to act upstream of or within maintenance of synapse structure; motor learning; and neuron remodeling. Predicted to be located in several cellular components, including climbing fiber; extracellular region; and presynapse. Predicted to be part of collagen trimer. Predicted to be active in cerebellar climbing fiber to Purkinje cell synapse and synaptic cleft. [provided by Alliance of Genome Resources, Apr 2025]
Canonical amino-acid sequenceUniProt
258 residues, UniProt reviewed canonical sequence.
>O75973|C1QL1
1 MLLVLVVLIP VLVSSGGPEG HYEMLGTCRM VCDPYPARGP GAGARTDGGD ALSEQSGAPP
61 PSTLVQGPQG KPGRTGKPGP PGPPGDPGPP GPVGPPGEKG EPGKPGPPGL PGAGGSGAIS
121 TATYTTVPRV AFYAGLKNPH EGYEVLKFDD VVTNLGNNYD AASGKFTCNI PGTYFFTYHV
181 LMRGGDGTSM WADLCKNGQV RASAIAQDAD QNYDYASNSV ILHLDAGDEV FIKLDGGKAH
241 GGNSNKYSTF SGFIIYSDLocalizationUniProt · AlphaFold · HPA
Whether an antibody against C1QL1 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Secreted
- Secreted
- Yes
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.5
- Highest tissue expression
- 42 nTPM
Expression across tissuesHPA
Tissue
- amygdala: 42 nTPM
- hypothalamus: 34 nTPM
- cerebral cortex: 34 nTPM
- hippocampal formation: 31 nTPM
- midbrain: 31 nTPM
- spinal cord: 27 nTPM
Single-cell type
- retinal horizontal cells: 435 nCPM
- oligodendrocyte progenitor cells: 186 nCPM
- retinal amacrine cells: 111 nCPM
- pancreatic islet cells: 82 nCPM
- podocytes: 74 nCPM
- mesothelial cells: 38 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- medulla oblongata: 286 nTPM
- cerebral cortex: 95 nTPM
- midbrain: 91 nTPM
- spinal cord: 73 nTPM
- cerebellum: 59 nTPM
- white matter: 54 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 1.91
- gnomAD pLI
- 0
- gnomAD missense Z
- 1.25
- DepMap mean gene effect
- 0.01
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- locomotory behavior
- maintenance of synapse structure
- motor learning
- neuron remodeling
- regulation of synapse pruning
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of C1QL1 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads C1QL1 as an antibody target. Whether an autoantibody or antibody against C1QL1 could matter depends on whether native C1QL1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
C1QL1 is annotated as secreted, so native C1QL1 circulates and is directly accessible to antibodies. Secreted and cell-surface proteins are the autoantibody targets most likely to act like drugs, blocking or depleting the native protein.
Annotation status
The present source text does not explicitly label C1QL1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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