LSM12
Protein LSM12
Also known as: FLJ30656, LSM12_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q3MHD2
- Gene
- LSM12
- Ensembl
- ENSG00000161654
- Chromosome
- 17
- Canonical length
- 195 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Cytosol
OverviewNCBI Gene
Predicted to enable RNA binding activity. Located in cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
195 residues, UniProt reviewed canonical sequence.
>Q3MHD2|LSM12
1 MAAPPGEYFS VGSQVSCRTC QEQRLQGEVV AFDYQSKMLA LKCPSSSGKP NHADILLINL
61 QYVSEVEIIN DRTETPPPLA SLNVSKLASK ARTEKEEKLS QAYAISAGVS LEGQQLFQTI
121 HKTIKDCKWQ EKNIVVMEEV VITPPYQVEN CKGKEGSALS HVRKIVEKHF RDVESQKILQ
181 RSQAQQPQKE AALSSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against LSM12 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)
- 0.39
- Highest tissue expression
- 32 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 32 nTPM
- retina: 29 nTPM
- bone marrow: 28 nTPM
- liver: 27 nTPM
- esophagus: 24 nTPM
- epididymis: 24 nTPM
Single-cell type
- tuft cells: 58 nCPM
- cone photoreceptor cells: 54 nCPM
- myonuclei: 44 nCPM
- rod photoreceptor cells: 37 nCPM
- renal collecting duct intercalated cells: 37 nCPM
- early spermatids: 27 nCPM
Immune cell
- intermediate monocyte: 80 nTPM
- non-classical monocyte: 79 nTPM
- plasmacytoid DC: 72 nTPM
- myeloid DC: 71 nTPM
- classical monocyte: 62 nTPM
- total PBMC: 61 nTPM
Brain region
- cerebral cortex: 38 nTPM
- hypothalamus: 37 nTPM
- midbrain: 36 nTPM
- thalamus: 33 nTPM
- medulla oblongata: 32 nTPM
- pons: 32 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)
- 0.27
- gnomAD pLI
- 0.97
- gnomAD missense Z
- 1.89
- DepMap mean gene effect
- -0.49
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of LSM12 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 LSM12 as an antibody target. Whether an autoantibody or antibody against LSM12 could matter depends on whether native LSM12 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
LSM12 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 LSM12 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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