Seroatlas · Human Serome Atlas

LRRC63

Leucine-rich repeat-containing protein 63

Also known as: LRC63_HUMAN

Cross-references: UniProt · GeneCards · NCBI Gene

Protein identityUniProt · HPA

UniProt accession
Q05C16
Gene
LRRC63
Canonical length
587 aa
Protein class
Predicted intracellular proteins

OverviewNCBI Gene

No narrative summary is available for LRRC63 in this catalog release; identity and structured annotations are shown without generated factual claims.

Canonical amino-acid sequenceUniProt

587 residues, UniProt reviewed canonical sequence.

>Q05C16|LRRC63
     1  MQKPPLLLRR PLPPKFTKLS LHEKKTHTAK TGKIESLHVA FTEDETTSIK MDRTRFPDVL
    61  RNQSLTPINI QNIFLDHCVQ ERVTAISSPQ KSTKHVREQI PDTATGSIFF PHCNSASTRI
   121  FGKQTNKMES SRKFKTMKDV YTEKRLENIL ILSSKFSKPK STPGSVIAQK LEKMHPKHQP
   181  LPESPGYTYQ HISRDLSATV PSPPPMTVSM KPEGQWPEHF KSTATLTLRV TEFPGFVSLP
   241  TPVLPRKPHR QSVIETLVTE NGNIESVPKQ IPPRPPEGLT KTEKIESEIH VVRGEGFKTV
   301  AATRYETITA MTNLAIVNCQ VYGRNALNLK GFFILNCPDL TPLAFQLIYL NLSFNDLHYF
   361  PTEILCLKNL QILKLRNNPI KEIPSEIQQL EFLRIFTIAF NLITVLPIGL FSLSYLEELD
   421  VSYNELTFIP NEIQKLRSLE KLTVDGNELS FFPHGILKLN LTKIQFENNF THPCFWRDNY
   481  LNNPQQLTQI ISLFIVQNKL HKFYDKIPVE VQKLLKCTSR CEWCHGPKFG EGFRVIRSCD
   541  IFGASQLPVM FYVCSPSCYR RIKESSFVLD GSPSRRIALD VELSKEL

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against LRRC63 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)
0.5
Highest tissue expression
9.9 nTPM

Expression across tissuesHPA

Tissue

  • spinal cord: 9.9 nTPM
  • midbrain: 3.5 nTPM
  • testis: 3.2 nTPM
  • epididymis: 2.2 nTPM
  • retina: 2.2 nTPM
  • hippocampal formation: 1.6 nTPM

Single-cell type

  • oligodendrocytes: 203 nCPM
  • early spermatids: 130 nCPM
  • ependymal cells: 96 nCPM
  • late primary spermatocytes: 76 nCPM
  • respiratory ciliated cells: 73 nCPM
  • fallopian tube ciliated cells: 48 nCPM

Immune cell

  • plasmacytoid DC: 0.5 nTPM
  • memory CD8 T-cell: 0.3 nTPM
  • naive CD4 T-cell: 0.2 nTPM
  • naive CD8 T-cell: 0.2 nTPM
  • gdT-cell: 0.1 nTPM
  • MAIT T-cell: 0.1 nTPM

Brain region

  • white matter: 20 nTPM
  • medulla oblongata: 14 nTPM
  • pons: 10 nTPM
  • cerebellum: 9.8 nTPM
  • basal ganglia: 9.6 nTPM
  • spinal cord: 9.4 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)
0.95
gnomAD pLI
0
gnomAD missense Z
0.96
DepMap mean gene effect
0.12
DepMap dependency class
none

OntologyGO

Biological processes

Protein domainsUniProt · Pfam · InterPro

KeywordsUniProt

Antibody and autoantibody relevanceSeroatlas analysis

Seroatlas reads LRRC63 as an antibody target. Whether an autoantibody or antibody against LRRC63 could matter depends on whether native LRRC63 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

LRRC63 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 LRRC63 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/LRRC63. 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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