CELF3
CUGBP Elav-like family member 3
Also known as: BRUNOL1, CAGH4, CELF3_HUMAN, ERDA4, MGC57297, TNRC4
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q5SZQ8
- Gene
- CELF3
- Ensembl
- ENSG00000159409
- Chromosome
- 1
- Canonical length
- 465 aa
- Protein class
- 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. Multiple alternatively spliced transcript variants encoding different isoforms have been identified in this gene. [provided by RefSeq, Feb 2010]
Canonical amino-acid sequenceUniProt
465 residues, UniProt reviewed canonical sequence.
>Q5SZQ8|CELF3
1 MKEPDAIKLF VGQIPRHLEE KDLKPIFEQF GRIFELTVIK DKYTGLHKGC AFLTYCARDS
61 ALKAQSALHE QKTLPGMNRP IQVKPADSES RGEDRKLFVG MLGKQQTDED VRKMFEPFGT
121 IDECTVLRGP DGTSKGCAFV KFQTHAEAQA AINTLHSSRT LPGASSSLVV KFADTEKERG
181 LRRMQQVATQ LGMFSPIALQ FGAYSAYTQA LMQQQAALVA AHSAYLSPMA TMAAVQMQHM
241 AAINANGLIA TPITPSSGTS TPPAIAATPV SAIPAALGVN GYSPVPTQPT GQPAPDALYP
301 NGVHPYPAQS PAAPVDPLQQ AYAGMQHYTA AYPAAYSLVA PAFPQPPALV AQQPPPPPQQ
361 QQQQQQQQQQ QQQREGPDGC NIFIYHLPQE FTDSEILQMF VPFGHVISAK VFVDRATNQS
421 KCFGFVSFDN PASAQAAIQA MNGFQIGMKR LKVQLKRPKD ANRPYLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CELF3 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)
- 0.47
- Highest tissue expression
- 105 nTPM
Expression across tissuesHPA
Tissue
- pituitary gland: 105 nTPM
- cerebellum: 99 nTPM
- basal ganglia: 85 nTPM
- cerebral cortex: 81 nTPM
- hippocampal formation: 72 nTPM
- amygdala: 71 nTPM
Single-cell type
- retinal bipolar cells: 101 nCPM
- lactotrophs: 86 nCPM
- adrenal medulla cells: 75 nCPM
- neuroendocrine cells: 55 nCPM
- thyrotrophs: 53 nCPM
- cone photoreceptor cells: 44 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
- cerebral cortex: 123 nTPM
- hippocampal formation: 118 nTPM
- amygdala: 105 nTPM
- basal ganglia: 102 nTPM
- hypothalamus: 97 nTPM
- cerebellum: 62 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)
- 0.39
- gnomAD pLI
- 0.77
- gnomAD missense Z
- 3.3
- DepMap mean gene effect
- -0.03
- 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
- flagellated sperm motility
- lncRNA transcription
- mRNA splice site recognition
- positive regulation of mRNA splicing, via spliceosome
- regulation of alternative mRNA splicing, via spliceosome
- RNA splicing
- spermatogenesis
- nuclear body organization
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads CELF3 as an antibody target. Whether an autoantibody or antibody against CELF3 could matter depends on whether native CELF3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CELF3 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 CELF3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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