CELF5
CUGBP Elav-like family member 5
Also known as: BRUNOL5, CELF5_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8N6W0
- Gene
- CELF5
- Ensembl
- ENSG00000161082
- Chromosome
- 19
- Canonical length
- 485 aa
- Protein class
- Predicted intracellular proteins
OverviewNCBI Gene
This gene encodes a member of the the CELF/BRUNOL protein family, which 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. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2012]
Canonical amino-acid sequenceUniProt
485 residues, UniProt reviewed canonical sequence.
>Q8N6W0|CELF5
1 MARLTESEAR RQQQQLLQPR PSPVGSSGPE PPGGQPDGMK DLDAIKLFVG QIPRHLDEKD
61 LKPLFEQFGR IYELTVLKDP YTGMHKGCAF LTYCARDSAI KAQTALHEQK TLPGMARPIQ
121 VKPADSESRG GRDRKLFVGM LNKQQSEEDV LRLFQPFGVI DECTVLRGPD GSSKGCAFVK
181 FSSHTEAQAA IHALHGSQTM PGASSSLVVK FADTDKERTL RRMQQMVGQL GILTPSLTLP
241 FSPYSAYAQA LMQQQTTVLS TSGSYLSPGV AFSPCHIQQI GAVSLNGLPA TPIAPASGLH
301 SPPLLGTTAV PGLVAPITNG FAGVVPFPGG HPALETVYAN GLVPYPAQSP TVAETLHPAF
361 SGVQQYTAMY PTAAITPIAH SVPQPPPLLQ QQQREGPEGC NLFIYHLPQE FGDTELTQMF
421 LPFGNIISSK VFMDRATNQS KCFGFVSFDN PASAQAAIQA MNGFQIGMKR LKVQLKRPKD
481 PGHPYLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CELF5 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)
- 0.49
- Highest tissue expression
- 23 nTPM
Expression across tissuesHPA
Tissue
- cerebellum: 23 nTPM
- basal ganglia: 22 nTPM
- cerebral cortex: 22 nTPM
- hypothalamus: 14 nTPM
- amygdala: 11 nTPM
- hippocampal formation: 9.2 nTPM
Single-cell type
- brain inhibitory neurons: 191 nCPM
- retinal amacrine cells: 185 nCPM
- brain excitatory neurons: 148 nCPM
- other brain neurons: 146 nCPM
- retinal bipolar cells: 141 nCPM
- oligodendrocyte progenitor 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: 89 nTPM
- hypothalamus: 75 nTPM
- basal ganglia: 75 nTPM
- hippocampal formation: 63 nTPM
- amygdala: 62 nTPM
- white matter: 39 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)
- 0.2
- gnomAD pLI
- 1
- gnomAD missense Z
- 3.69
- DepMap mean gene effect
- -0.12
- 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
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads CELF5 as an antibody target. Whether an autoantibody or antibody against CELF5 could matter depends on whether native CELF5 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CELF5 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 CELF5 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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