Seroatlas · Human Serome Atlas

LIPJ

Lipase member J

Also known as: bA425M17.2, LIPJ_HUMAN, LIPL1

Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene

Protein identityUniProt · HPA

UniProt accession
Q5W064
Gene
LIPJ
Ensembl
ENSG00000204022
Chromosome
10
Canonical length
366 aa
Protein class
Predicted intracellular proteins
Subcellular location
Plasma membrane

OverviewNCBI Gene

Predicted to enable hydrolase activity, acting on ester bonds. Predicted to be involved in lipid catabolic process. Predicted to be active in intracellular membrane-bounded organelle. [provided by Alliance of Genome Resources, Apr 2025]

Canonical amino-acid sequenceUniProt

366 residues, UniProt reviewed canonical sequence.

>Q5W064|LIPJ
     1  MNISQIISYW GYPDEEYDIV TEDGYILGLY RIPYWRTDNN KNLAQRVVVY LQHGLLTSAS
    61  SWISNLPNNS LGFILADAGY DVWMGNSRGN TWSRKHLYLE TSSKEFWAFS FDEMAKYDLP
   121  ASIDFTVKQT RQEEIFYVGH SQGTTIGFIT FSTISKIAER IKIFFALAPV FSTKYLKSPL
   181  IRMTYKWKSI VMAFSGNKDF LPKTSFKKFI GSKLCPLQIF DKICLNILFM MFGYDPKNLN
   241  MSRLDVYFSH NPAGTSVQNM LHWSQLLNST HLKAYDWGSP DLNLVHYNQT TSPLYNMTNM
   301  NVATAIWNGK SDLLADPEDV NILHSEITNH IYYKTISYYN HIDSLFGLDV YDQVYHEIID
   361  IIQDNL

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against LIPJ 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
Unknown
Secreted
No
Transmembrane segments
0
Mean surface accessibility (rSASA)
0.21
Highest tissue expression
6.5 nTPM

Expression across tissuesHPA

Tissue

  • testis: 6.5 nTPM
  • epididymis: 0.8 nTPM
  • fallopian tube: 0.6 nTPM
  • cerebellum: 0.5 nTPM
  • liver: 0.5 nTPM
  • thyroid gland: 0.5 nTPM

Single-cell type

  • late primary spermatocytes: 85 nCPM
  • early spermatids: 41 nCPM
  • ependymal cells: 28 nCPM
  • tuft cells: 12 nCPM
  • late spermatids: 9 nCPM
  • thymic myoid cells: 8.2 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

  • medulla oblongata: 2.7 nTPM
  • cerebellum: 2.3 nTPM
  • midbrain: 1.3 nTPM
  • spinal cord: 0.9 nTPM
  • choroid plexus: 0.8 nTPM
  • hippocampal formation: 0.7 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)
1.21
gnomAD pLI
0
gnomAD missense Z
0.2
DepMap mean gene effect
0.09
DepMap dependency class
none

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

Protein domainsUniProt · Pfam · InterPro

KeywordsUniProt

Antibody and autoantibody relevanceSeroatlas analysis

Seroatlas reads LIPJ as an antibody target. Whether an autoantibody or antibody against LIPJ could matter depends on whether native LIPJ is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

LIPJ 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 LIPJ as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/LIPJ. Study-independent annotations aggregated from UniProt, Human Protein Atlas, PubMed, IEDB, Pfam, InterPro, Gene Ontology, AlphaFold, gnomAD, DepMap, ClinVar, TCGA. Catalog release seroatlas-reviewed-human-uniprot-20260313.

Seroatlas is the reference for exploring autoantibody and antibody serology at the human-protein level: the autoreactome and human serome, multiplex serology (HuProt, HuScan, VirScan, PhIP-Seq).

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