LUC7L2
Putative RNA-binding protein Luc7-like 2
Also known as: CGI-59, CGI-74, FLJ10657, H_NH0792N18.3, hLuc7B2, LC7L2_HUMAN, LUC7B2
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9Y383
- Gene
- LUC7L2
- Ensembl
- ENSG00000146963
- Chromosome
- 7
- Canonical length
- 392 aa
- Protein class
- Plasma proteins, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm
OverviewNCBI Gene
This gene encodes a protein that contains a C2H2-type zinc finger, coiled-coil region and arginine, serine-rich (RS) domain. A similar protein in mouse interacts with sodium channel modifier 1, and the encoded protein may be involved in the recognition of non-consensus splice donor sites in association with the U1 snRNP spliceosomal subunit. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Sep 2011]
Canonical amino-acid sequenceUniProt
392 residues, UniProt reviewed canonical sequence.
>Q9Y383|LUC7L2
1 MSAQAQMRAM LDQLMGTSRD GDTTRQRIKF SDDRVCKSHL LNCCPHDVLS GTRMDLGECL
61 KVHDLALRAD YEIASKEQDF FFELDAMDHL QSFIADCDRR TEVAKKRLAE TQEEISAEVA
121 AKAERVHELN EEIGKLLAKV EQLGAEGNVE ESQKVMDEVE KARAKKREAE EVYRNSMPAS
181 SFQQQKLRVC EVCSAYLGLH DNDRRLADHF GGKLHLGFIE IREKLEELKR VVAEKQEKRN
241 QERLKRREER EREEREKLRR SRSHSKNPKR SRSREHRRHR SRSMSRERKR RTRSKSREKR
301 HRHRSRSSSR SRSRSHQRSR HSSRDRSRER SKRRSSKERF RDQDLASCDR DRSSRDRSPR
361 DRDRKDKKRS YESANGRSED RRSSEEREAG EILocalizationUniProt · AlphaFold · HPA
Whether an antibody against LUC7L2 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
- 75 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 75 nTPM
- skeletal muscle: 60 nTPM
- thymus: 58 nTPM
- thyroid gland: 57 nTPM
- blood vessel: 56 nTPM
- spinal cord: 51 nTPM
Single-cell type
- oligodendrocytes: 315 nCPM
- bergmann glia: 248 nCPM
- brain excitatory neurons: 244 nCPM
- brain inhibitory neurons: 235 nCPM
- choroid plexus epithelial cells: 228 nCPM
- other brain neurons: 224 nCPM
Immune cell
- naive CD4 T-cell: 21 nTPM
- MAIT T-cell: 20 nTPM
- T-reg: 19 nTPM
- memory CD8 T-cell: 19 nTPM
- naive CD8 T-cell: 18 nTPM
- eosinophil: 18 nTPM
Brain region
- white matter: 78 nTPM
- cerebral cortex: 77 nTPM
- hypothalamus: 72 nTPM
- cerebellum: 63 nTPM
- thalamus: 61 nTPM
- basal ganglia: 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)
- 0.65
- gnomAD pLI
- 0
- gnomAD missense Z
- 2.19
- DepMap mean gene effect
- -0.23
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 9% 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
InteractionsUniProt · HPA
Protein binding partners of LUC7L2 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 LUC7L2 as an antibody target. Whether an autoantibody or antibody against LUC7L2 could matter depends on whether native LUC7L2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
LUC7L2 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 LUC7L2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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