LSM14B
Protein LSM14 homolog B
Also known as: bA11M20.3, C20orf40, FAM61B, FLJ25473, FT005, LS14B_HUMAN, LSM13, RAP55B
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9BX40
- Gene
- LSM14B
- Ensembl
- ENSG00000149657
- Chromosome
- 20
- Canonical length
- 385 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Vesicles
OverviewNCBI Gene
Enables RNA binding activity. Predicted to be involved in several processes, including maternal mRNA clearance; meiotic cell cycle process involved in oocyte maturation; and ovarian follicle development. Predicted to be located in cytoplasmic ribonucleoprotein granule. Predicted to be part of ribonucleoprotein complex. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
385 residues, UniProt reviewed canonical sequence.
>Q9BX40|LSM14B
1 MSGSSGTPYL GSKISLISKA QIRYEGILYT IDTDNSTVAL AKVRSFGTED RPTDRPAPPR
61 EEIYEYIIFR GSDIKDITVC EPPKAQHTLP QDPAIVQSSL GSASASPFQP HVPYSPFRGM
121 APYGPLAASS LLSQQYAASL GLGAGFPSIP VGKSPMVEQA VQTGSADNLN AKKLLPGKGT
181 TGTQLNGRQA QPSSKTASDV VQPAAVQAQG QVNDENRRPQ RRRSGNRRTR NRSRGQNRPT
241 NVKENTIKFE GDFDFESANA QFNREELDKE FKKKLNFKDD KAEKGEEKDL AVVTQSAEAP
301 AEEDLLGPNC YYDKSKSFFD NISSELKTSS RRTTWAEERK LNTETFGVSG RFLRGRSSRG
361 GFRGGRGNGT TRRNPTSHRA GTGRVLocalizationUniProt · AlphaFold · HPA
Whether an antibody against LSM14B 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
- Other membrane
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.63
- Highest tissue expression
- 70 nTPM
Expression across tissuesHPA
Tissue
- cerebellum: 70 nTPM
- skeletal muscle: 67 nTPM
- testis: 49 nTPM
- tongue: 42 nTPM
- cerebral cortex: 39 nTPM
- heart muscle: 35 nTPM
Single-cell type
- late spermatids: 902 nCPM
- early spermatids: 287 nCPM
- megakaryocytes: 37 nCPM
- late primary spermatocytes: 37 nCPM
- medullary thymic epithelial cells: 31 nCPM
- thymic myoid cells: 26 nCPM
Immune cell
- eosinophil: 2.3 nTPM
- neutrophil: 0.6 nTPM
- memory B-cell: 0.5 nTPM
- naive B-cell: 0.5 nTPM
- classical monocyte: 0.4 nTPM
- memory CD8 T-cell: 0.4 nTPM
Brain region
- cerebellum: 85 nTPM
- cerebral cortex: 70 nTPM
- hippocampal formation: 66 nTPM
- basal ganglia: 64 nTPM
- amygdala: 60 nTPM
- thalamus: 60 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)
- 0.23
- gnomAD pLI
- 1
- gnomAD missense Z
- 1.69
- DepMap mean gene effect
- 0.07
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 17% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- meiotic cell cycle process involved in oocyte maturation
- membraneless organelle assembly
- oogenesis
- ovarian follicle development
- regulation of translation
- maternal mRNA clearance
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of LSM14B 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 LSM14B as an antibody target. Whether an autoantibody or antibody against LSM14B could matter depends on whether native LSM14B is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
LSM14B 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 LSM14B as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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