CELF1
CUGBP Elav-like family member 1
Also known as: BRUNOL2, CELF1_HUMAN, CUG-BP, CUGBP, CUGBP1, EDEN-BP, hNab50, NAB50, NAPOR
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q92879
- Gene
- CELF1
- Ensembl
- ENSG00000149187
- Chromosome
- 11
- Canonical length
- 486 aa
- Protein class
- Plasma proteins, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm
OverviewNCBI Gene
Members of the CELF/BRUNOL protein family contain two N-terminal RNA recognition motif (RRM) domains, one C-terminal RRM domain, and a divergent segment of 160-230 aa between the second and third RRM domains. Members of this protein family regulate pre-mRNA alternative splicing and may also be involved in mRNA editing, and translation. This gene may play a role in myotonic dystrophy type 1 (DM1) via interactions with the dystrophia myotonica-protein kinase (DMPK) gene. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
486 residues, UniProt reviewed canonical sequence.
>Q92879|CELF1
1 MNGTLDHPDQ PDLDAIKMFV GQVPRTWSEK DLRELFEQYG AVYEINVLRD RSQNPPQSKG
61 CCFVTFYTRK AALEAQNALH NMKVLPGMHH PIQMKPADSE KNNAVEDRKL FIGMISKKCT
121 ENDIRVMFSS FGQIEECRIL RGPDGLSRGC AFVTFTTRAM AQTAIKAMHQ AQTMEGCSSP
181 MVVKFADTQK DKEQKRMAQQ LQQQMQQISA ASVWGNLAGL NTLGPQYLAL YLQLLQQTAS
241 SGNLNTLSSL HPMGGLNAMQ LQNLAALAAA ASAAQNTPSG TNALTTSSSP LSVLTSSGSS
301 PSSSSSNSVN PIASLGALQT LAGATAGLNV GSLAGMAALN GGLGSSGLSN GTGSTMEALT
361 QAYSGIQQYA AAALPTLYNQ NLLTQQSIGA AGSQKEGPEG ANLFIYHLPQ EFGDQDLLQM
421 FMPFGNVVSA KVFIDKQTNL SKCFGFVSYD NPVSAQAAIQ SMNGFQIGMK RLKVQLKRSK
481 NDSKPYLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CELF1 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
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.48
- Highest tissue expression
- 62 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 62 nTPM
- cerebellum: 49 nTPM
- tongue: 49 nTPM
- liver: 48 nTPM
- parathyroid gland: 40 nTPM
- bone marrow: 40 nTPM
Single-cell type
- neutrophils: 636 nCPM
- neutrophil progenitors: 399 nCPM
- hepatocytes: 336 nCPM
- choroid plexus epithelial cells: 330 nCPM
- sertoli cells: 320 nCPM
- monocytes: 305 nCPM
Immune cell
- eosinophil: 23 nTPM
- non-classical monocyte: 18 nTPM
- MAIT T-cell: 16 nTPM
- naive B-cell: 15 nTPM
- neutrophil: 15 nTPM
- memory CD8 T-cell: 14 nTPM
Brain region
- cerebellum: 132 nTPM
- basal ganglia: 107 nTPM
- amygdala: 92 nTPM
- choroid plexus: 91 nTPM
- cerebral cortex: 89 nTPM
- hippocampal formation: 88 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)
- 0.17
- gnomAD pLI
- 1
- gnomAD missense Z
- 3.34
- DepMap mean gene effect
- -0.19
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- embryo development ending in birth or egg hatching
- germ cell development
- mRNA destabilization
- mRNA processing
- mRNA splice site recognition
- negative regulation of cell population proliferation
- negative regulation of gene expression
- positive regulation of gene expression
- post-transcriptional gene silencing
- regulation of alternative mRNA splicing, via spliceosome
- regulation of inflammatory response
- regulation of RNA splicing
- regulatory ncRNA-mediated post-transcriptional gene silencing
Molecular functions
- BRE binding
- mRNA 3'-UTR binding
- mRNA binding
- mRNA regulatory element binding translation repressor activity
- pre-mRNA binding
- RNA binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of CELF1 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 CELF1 as an antibody target. Whether an autoantibody or antibody against CELF1 could matter depends on whether native CELF1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CELF1 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label CELF1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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