LRRC14
Leucine-rich repeat-containing protein 14
Also known as: KIAA0014, LRC14_HUMAN, LRRC14A
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q15048
- Gene
- LRRC14
- Ensembl
- ENSG00000160959
- Chromosome
- 8
- Canonical length
- 493 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Cytosol
OverviewNCBI Gene
This gene encodes a leucine-rich repeat-containing protein. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Dec 2012]
Canonical amino-acid sequenceUniProt
493 residues, UniProt reviewed canonical sequence.
>Q15048|LRRC14
1 MHTLVFLSTR QVLQCQPAAC QALPLLPREL FPLLFKVAFM DKKTVVLREL VHTWPFPLLS
61 FQQLLQECAH CSRALLQERP STESMQAVIL GLTARLHTSE PGASTQPLCR KHALRVLDMT
121 GLLDDGVEQD PGTMSMWDCT AAVARTCIAQ QQGGAAEPGP APIPVEVRVD LRVNRASYAF
181 LREALRSSVG SPLRLCCRDL RAEDLPMRNT VALLQLLDAG CLRRVDLRFN NLGLRGLSVI
241 IPHVARFQHL ASLRLHYVHG DSRQPSVDGE DNFRYFLAQM GRFTCLRELS MGSSLLSGRL
301 DQLLSTLQSP LESLELAFCA LLPEDLRFLA RSPHAAHLKK LDLSGNDLSG SQLAPFQGLL
361 QASAATLLHL ELTECQLADT QLLATLPILT QCASLRYLGL YGNPLSMAGL KELLRDSVAQ
421 AELRTVVHPF PVDCYEGLPW PPPASVLLEA SINEEKFARV EAELHQLLLA SGRAHVLWTT
481 DIYGRLAADY FSLLocalizationUniProt · AlphaFold · HPA
Whether an antibody against LRRC14 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)
- 0.25
- Highest tissue expression
- 19 nTPM
Expression across tissuesHPA
Tissue
- cerebral cortex: 19 nTPM
- prostate: 18 nTPM
- cerebellum: 16 nTPM
- thyroid gland: 16 nTPM
- pancreas: 15 nTPM
- endometrium: 15 nTPM
Single-cell type
- early primary spermatocytes: 29 nCPM
- differentiating spermatogonia: 28 nCPM
- epididymal principal cells: 20 nCPM
- respiratory ionocytes: 18 nCPM
- plasma cells: 15 nCPM
- enteric transient amplifying cells: 15 nCPM
Immune cell
- NK-cell: 12 nTPM
- gdT-cell: 8.4 nTPM
- plasmacytoid DC: 8.4 nTPM
- MAIT T-cell: 8 nTPM
- total PBMC: 8 nTPM
- naive B-cell: 7.9 nTPM
Brain region
- cerebellum: 40 nTPM
- hippocampal formation: 34 nTPM
- cerebral cortex: 33 nTPM
- white matter: 31 nTPM
- amygdala: 31 nTPM
- medulla oblongata: 30 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)
- 1.03
- gnomAD pLI
- 0
- gnomAD missense Z
- 1.16
- DepMap mean gene effect
- 0.02
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 14% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- negative regulation of NF-kappaB transcription factor activity
- negative regulation of toll-like receptor signaling pathway
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of LRRC14 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 LRRC14 as an antibody target. Whether an autoantibody or antibody against LRRC14 could matter depends on whether native LRRC14 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
LRRC14 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 LRRC14 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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