LAYN

gene
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Also known as FLJ30977FLJ31092

Summary

LAYN (layilin, HGNC:29471) is a protein-coding gene on chromosome 11q23.1, encoding Layilin (Q6UX15). Receptor for hyaluronate.

Enables hyaluronic acid binding activity. Located in focal adhesion.

Source: NCBI Gene 143903 — RefSeq curated summary.

At a glance

  • GWAS associations: 10
  • Clinical variants (ClinVar): 78 total
  • MANE Select transcript: NM_178834

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:29471
Approved symbolLAYN
Namelayilin
Location11q23.1
Locus typegene with protein product
StatusApproved
AliasesFLJ30977, FLJ31092
Ensembl geneENSG00000204381
Ensembl biotypeprotein_coding
OMIM618843
Entrez143903

Gene structure

Transcript identifiers

Ensembl transcripts: 14 — 12 protein_coding, 1 nonsense_mediated_decay, 1 protein_coding_CDS_not_defined

ENST00000375614, ENST00000375615, ENST00000436913, ENST00000525126, ENST00000525866, ENST00000528102, ENST00000528924, ENST00000530962, ENST00000533265, ENST00000533999, ENST00000851628, ENST00000851629, ENST00000851630, ENST00000935731

RefSeq mRNA: 4 — MANE Select: NM_178834 NM_001258390, NM_001258391, NM_001318799, NM_178834

CCDS: CCDS31676, CCDS58178, CCDS58179

Canonical transcript exons

ENST00000375614 — 7 exons

ExonStartEnd
ENSE00003503128111554561111554593
ENSE00003504896111560095111561745
ENSE00003537210111549618111549775
ENSE00003560918111540720111540928
ENSE00003573304111543923111544220
ENSE00003679299111555207111555290
ENSE00003789150111557541111557643

Expression profiles

Bgee: expression breadth ubiquitous, 225 present calls, max score 96.36.

FANTOM5 (CAGE): breadth ubiquitous, TPM avg 18.5099 / max 288.0773, expressed in 1310 samples.

FANTOM5 promoters (4 alternative TSS)

Promoter IDTPM avgSamples expressed
11662717.98651307
1166280.2612158
1166290.2236110
1166260.038610

Top tissues by expression

248 total, by Bgee expression score (0-100, higher = more expressed):

TissueAnatomy IDExpression scoreQuality
deciduaUBERON:000245096.36gold quality
stromal cell of endometriumCL:000225593.81gold quality
amniotic fluidUBERON:000017393.38gold quality
ascending aortaUBERON:000149690.67gold quality
thoracic aortaUBERON:000151590.58gold quality
epithelial cell of pancreasCL:000008390.39gold quality
descending thoracic aortaUBERON:000234590.32gold quality
muscle layer of sigmoid colonUBERON:003580588.54gold quality
smooth muscle tissueUBERON:000113588.24gold quality
urethraUBERON:000005788.16gold quality
left ovaryUBERON:000211987.97gold quality
aortaUBERON:000094787.54gold quality
olfactory segment of nasal mucosaUBERON:000538687.45gold quality
gall bladderUBERON:000211087.23gold quality
right ovaryUBERON:000211886.59gold quality
left lobe of thyroid glandUBERON:000112086.26gold quality
thyroid glandUBERON:000204686.16gold quality
calcaneal tendonUBERON:000370186.07gold quality
corpus callosumUBERON:000233685.99gold quality
body of uterusUBERON:000985385.81gold quality
left uterine tubeUBERON:000130385.70gold quality
right lobe of thyroid glandUBERON:000111985.36gold quality
tibial arteryUBERON:000761085.30gold quality
popliteal arteryUBERON:000225085.29gold quality
ovaryUBERON:000099285.25gold quality
germinal epithelium of ovaryUBERON:000130485.25gold quality
visceral pleuraUBERON:000240184.82gold quality
myometriumUBERON:000129684.57gold quality
mucosa of stomachUBERON:000119984.49gold quality
C1 segment of cervical spinal cordUBERON:000646984.06gold quality

Single-cell (SCXA)

Detected in 4 experiment(s), a significant marker in 4.

ExperimentMarker?Max mean expression
E-MTAB-11121yes486.14
E-HCAD-1yes17.40
E-CURD-88yes16.30
E-ANND-3yes5.73

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

62 targeting LAYN, top 30 by miRDB confidence (max_score; target_count = how many genes the miRNA targets in total — lower means more specific):

miRNAMax scoreAvg scoremiRNA target_count
HSA-MIR-3120-5P100.0065.56965
HSA-MIR-4283100.0066.422097
HSA-MIR-4795-3P100.0074.624024
HSA-MIR-520G-5P99.9966.76658
HSA-MIR-223-3P99.9970.141140
HSA-MIR-6888-3P99.9765.951170
HSA-MIR-3065-5P99.9771.563281
HSA-MIR-50799.9770.111915
HSA-MIR-568899.9673.234504
HSA-MIR-495-3P99.9672.814197
HSA-MIR-55799.9670.011640
HSA-MIR-570-3P99.9672.414910
HSA-MIR-651-3P99.9473.485177
HSA-MIR-450B-5P99.9271.483175
HSA-MIR-627-3P99.9071.423316
HSA-MIR-153-5P99.8973.866317
HSA-MIR-3617-5P99.7569.411968
HSA-MIR-64199.7569.351975
HSA-MIR-6885-3P99.7570.363187
HSA-MIR-3680-3P99.7572.513095
HSA-MIR-130399.6569.771662
HSA-MIR-466399.6265.33957
HSA-MIR-4743-3P99.6268.122095
HSA-MIR-510-3P99.5470.062965
HSA-MIR-391599.4568.491905
HSA-MIR-19A-5P99.3666.931675
HSA-MIR-4999-5P99.3569.15926
HSA-MIR-124499.3368.38832
HSA-MIR-133A-5P99.2869.13941
HSA-MIR-450599.2767.812678

Literature-anchored findings (GeneRIF, showing 10)

  • Hyaluronan and layilin mediate loss of airway epithelial barrier function induced by cigarette smoke by decreasing E-cadherin. (PMID:23048036)
  • results indicate that LAYN would be involved in the enhancement of inflammation and degradation of cartilage in joint diseases such as RA and OA (PMID:25150153)
  • Renal biopsy samples from patients with glomerulonephritis showed high expression of LAYN in tubular epithelial cells. (PMID:26410531)
  • increased LAYN expression correlates with poor prognosis and increased immune infiltration levels in CD8+ T cells, CD4+ T cells, macrophages, neutrophils and DCs of multiple cancers, especially in colon and gastric cancers. (PMID:30761122)
  • Layilin augments integrin activation to promote antitumor immunity. (PMID:32539073)
  • Layilin promotes mitochondrial fission by cyclin-dependent kinase 1 and dynamin-related protein 1 activation in HEK293T cells. (PMID:33676182)
  • ncRNA-Regulated LAYN Serves as a Prognostic Biomarker and Correlates with Immune Cell Infiltration in Hepatocellular Carcinoma: A Bioinformatics Analysis. (PMID:36398067)
  • Comprehensive landscape of the miRNA-regulated prognostic marker LAYN with immune infiltration and stemness in pan-cancer. (PMID:37335337)
  • Elevated Layilin-Positive Monocyte Levels in the Peripheral Blood of Patients with Systemic Lupus Erythematosus Reflect Their Autoimmune Status. (PMID:37642473)
  • Role of layilin in regulating mitochondria-mediated apoptosis: a study on B cell lymphoma (BCL)-2 family proteins. (PMID:39455917)

Cross-species orthologs

4 orthologs

OrganismSymbolGene ID
danio_reriolaynaENSDARG00000035169
danio_reriolaynbENSDARG00000056835
mus_musculusLaynENSMUSG00000060594
rattus_norvegicusLaynENSRNOG00000011228

Paralogs (1): CHODL (ENSG00000154645)

Protein

Protein identifiers

LayilinQ6UX15 (reviewed: Q6UX15)

All UniProt accessions (7): A0A0D9SFG0, E9PK64, E9PMI0, E9PQU7, E9PQY8, E9PR90, Q6UX15

UniProt curated annotations — full annotation on UniProt →

Function. Receptor for hyaluronate.

Subunit / interactions. Interacts with NF2, RDX and TLN1.

Subcellular location. Membrane.

Domain organisation. The C-terminal domain interacts with the N-terminal domain of RDX.

Isoforms (3)

UniProt IDNamesCanonical?
Q6UX15-11yes
Q6UX15-22
Q6UX15-33

RefSeq proteins (4): NP_001245319, NP_001245320, NP_001305728, NP_849156* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR001304C-type_lectin-likeDomain
IPR016186C-type_lectin-like/link_sfHomologous_superfamily
IPR016187CTDL_foldHomologous_superfamily
IPR051505C-type_lectin_domainFamily

Pfam: PF00059

UniProt features (27 total): repeat 5, region of interest 5, splice variant 3, modified residue 2, disulfide bond 2, topological domain 2, sequence conflict 2, signal peptide 1, chain 1, glycosylation site 1, sequence variant 1, transmembrane region 1, domain 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q6UX15-F169.270.34

Functional residue map

Curated UniProt residues grouped by drug-discovery relevance — catalytic, ligand-binding, modification, and mutation-validated positions. Source: UniProtKB sequence features.

Post-translational modifications (2): 286, 299

Disulfide bonds (2): 71–184, 150–176

Glycosylation sites (1): 117

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 85 (showing top): BENPORATH_ES_WITH_H3K27ME3, GOCC_CELL_SURFACE, GOCC_RUFFLE, CAGCTG_AP4_Q5, ATF1_Q6, GOMF_GLYCOSAMINOGLYCAN_BINDING, RYTTCCTG_ETS2_B, NERF_Q2, GOCC_ANCHORING_JUNCTION, MGGAAGTG_GABP_B, GOCC_CELL_LEADING_EDGE, GOMF_HYALURONIC_ACID_BINDING, HAMAI_APOPTOSIS_VIA_TRAIL_UP, DODD_NASOPHARYNGEAL_CARCINOMA_DN, CHEN_METABOLIC_SYNDROM_NETWORK

GO Biological Process (0):

GO Molecular Function (3): hyaluronic acid binding (GO:0005540), carbohydrate binding (GO:0030246), protein binding (GO:0005515)

GO Cellular Component (4): ruffle (GO:0001726), focal adhesion (GO:0005925), cell surface (GO:0009986), membrane (GO:0016020)

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
binding2
cellular anatomical structure2
carboxylic acid binding1
cell leading edge1
plasma membrane bounded cell projection1
cell-substrate junction1

Protein interactions and networks

STRING

596 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
LAYNTLN1Q9Y490947
LAYNTLN2Q9Y4G6940
LAYNNF2P35240828
LAYNRDXP35241758
LAYNLYVE1Q9Y5Y7546
LAYNMAGEH1Q9H213515
LAYNMSNP26038510
LAYNHMMRO75330507
LAYNEZRP15311481
LAYNTIGITQ495A1479
LAYNHAVCR2Q8TDQ0475
LAYNLAG3P18627471
LAYNGZMKP49863448
LAYNCTLA4P16410448
LAYNCCR8P51685446

IntAct

5 interactions, top by confidence:

ABTypeScore
KCNE3RIOK3psi-mi:“MI:0914”(association)0.530
LPAR1TMEM223psi-mi:“MI:0914”(association)0.530
SNAP23psi-mi:“MI:0914”(association)0.350
Ppsi-mi:“MI:0914”(association)0.350

BioGRID (30): LAYN (Reconstituted Complex), LAYN (Two-hybrid), LAYN (Two-hybrid), LAYN (Two-hybrid), DEFB121 (Two-hybrid), PPAPDC2 (Two-hybrid), LAYN (Affinity Capture-RNA), LAYN (Two-hybrid), NACA (Proximity Label-MS), TXNL1 (Proximity Label-MS), POLR1A (Proximity Label-MS), NACAP1 (Proximity Label-MS), BTF3 (Proximity Label-MS), HSPA8 (Proximity Label-MS), HSPA6 (Proximity Label-MS)

ESM2 similar proteins: A0JNA2, A2RRU4, A4FUY1, A5D7V5, A8MVS5, D4A6L0, E1BBQ2, O19131, O54693, O75144, P09564, P15151, P19438, P29590, P31994, P32506, P32507, P50555, P97260, Q14CZ8, Q28110, Q3TEW6, Q53EL9, Q5BJT4, Q5DRQ8, Q5T848, Q61190, Q640R3, Q6AYP5, Q6AYT8, Q6BAA4, Q6GQT6, Q6P6J9, Q6UX15, Q70EL4, Q75VT8, Q7TSK2, Q7Z692, Q8C419, Q8N126

Diamond homologs: A0ZT93, A5PMY6, A6QP79, B0VXV0, B0VXV1, D3ZWT9, O14594, P02707, P06734, P07307, P07897, P07898, P08290, P08661, P0DQV8, P10716, P13608, P13611, P16112, P20693, P22897, P24721, P41317, P48304, P49300, P49874, P50403, P55066, P55067, P55068, P70194, P81018, P81282, P82596, Q28062, Q28343, Q28670, Q29011, Q2LK54, Q2LK95

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

78 variants total. Per-class counts are floors (≥ shown; pagination cap):

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance66
Likely benign2
Benign4

Top pathogenic / likely-pathogenic (0)

SpliceAI

992 predictions. Top by Δscore:

VariantEffectΔscore
11:111540926:GTG:Gdonor_gain1.0000
11:111542801:G:GTdonor_gain1.0000
11:111554554:A:AGacceptor_gain1.0000
11:111554559:A:AGacceptor_gain1.0000
11:111554560:G:GGacceptor_gain1.0000
11:111554591:AAGGT:Adonor_loss1.0000
11:111554592:AGG:Adonor_loss1.0000
11:111554593:GGT:Gdonor_loss1.0000
11:111554594:GTA:Gdonor_loss1.0000
11:111554595:T:Adonor_loss1.0000
11:111555282:A:Tdonor_gain1.0000
11:111557538:CAGAA:Cacceptor_loss1.0000
11:111557539:A:AGacceptor_gain1.0000
11:111557540:G:GGacceptor_gain1.0000
11:111557540:GAA:Gacceptor_gain1.0000
11:111560093:A:AGacceptor_gain1.0000
11:111560094:G:GGacceptor_gain1.0000
11:111560094:GA:Gacceptor_gain1.0000
11:111560094:GAA:Gacceptor_gain1.0000
11:111540924:GAGTG:Gdonor_gain0.9900
11:111540929:G:GAdonor_loss0.9900
11:111540929:G:GGdonor_gain0.9900
11:111540930:TGAG:Tdonor_loss0.9900
11:111540931:GAGT:Gdonor_loss0.9900
11:111542797:TTAGG:Tdonor_gain0.9900
11:111549234:A:Gdonor_gain0.9900
11:111549744:G:GTdonor_gain0.9900
11:111554543:T:TAacceptor_gain0.9900
11:111554555:C:Gacceptor_gain0.9900
11:111554556:TACAG:Tacceptor_gain0.9900

AlphaMissense

2465 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
11:111549624:G:CW138C0.999
11:111549624:G:TW138C0.999
11:111549721:T:AW171R0.999
11:111549721:T:CW171R0.999
11:111549723:G:CW171C0.999
11:111549723:G:TW171C0.999
11:111544128:G:CW105C0.997
11:111544128:G:TW105C0.997
11:111544194:G:CW127C0.997
11:111544194:G:TW127C0.997
11:111549622:T:AW138R0.997
11:111549622:T:CW138R0.997
11:111549658:T:CC150R0.997
11:111549658:T:AC150S0.996
11:111549659:G:CC150S0.996
11:111549722:G:CW171S0.996
11:111549659:G:AC150Y0.995
11:111544126:T:AW105R0.994
11:111544126:T:CW105R0.994
11:111549660:C:GC150W0.994
11:111549736:T:AC176S0.994
11:111549737:G:CC176S0.994
11:111549760:T:AC184S0.994
11:111549761:G:CC184S0.994
11:111544192:T:AW127R0.993
11:111544192:T:CW127R0.993
11:111549726:T:AN172K0.993
11:111549726:T:GN172K0.993
11:111549659:G:TC150F0.992
11:111544026:C:GC71W0.991

dbSNP variants (sampled 300 via entrez): RS1000114802 (11:111551774 G>A,C,T), RS1000154255 (11:111543899 T>C), RS1000166849 (11:111551470 G>A,T), RS1000230443 (11:111550471 C>T), RS1000341042 (11:111545083 C>T), RS1000342014 (11:111557761 T>C), RS1000457093 (11:111538422 C>A), RS1000615343 (11:111543031 G>A), RS1000678311 (11:111556504 G>A), RS1001081371 (11:111543380 G>C), RS1001254155 (11:111538290 G>A), RS1001383934 (11:111550386 C>T), RS1001457908 (11:111558547 A>C), RS1001510336 (11:111558218 TTA>T), RS1001564440 (11:111557685 T>C)

Disease associations

OMIM: gene MIM:618843 | disease phenotypes:

GenCC curated gene-disease

Mondo (0):

Orphanet (0):

HPO phenotypes

0 total (0 of 0 shown, HPO-id order):

GWAS associations

10 associations (top):

StudyTraitp-value
GCST001762_38Obesity-related traits4.000000e-06
GCST005038_73Allergic disease (asthma, hay fever or eczema)7.000000e-15
GCST007563_14Allergic disease (asthma, hay fever or eczema)1.000000e-10
GCST007564_5Asthma or allergic disease (pleiotropy)6.000000e-11
GCST007798_134Asthma2.000000e-09
GCST007799_31Asthma (adult onset)6.000000e-09
GCST008103_146Bipolar disorder3.000000e-06
GCST010135_36Oily fish consumption9.000000e-09
GCST010140_26Pork consumption9.000000e-09
GCST010142_27Fish- and plant-related diet3.000000e-09

EFO canonical traits (3, from GWAS)

EFO IDTrait name
EFO:0004626IGFBP-3 measurement
EFO:1002011adult onset asthma
EFO:0008111diet measurement

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

PharmGKB: 1 entry (VIP=true, CPIC=false)

CTD chemical–gene interactions

32 total (human), top 30 by PubMed support.

ChemicalActions (top 5)PubMed papers
Valproic Acidincreases expression, affects expression, decreases methylation, affects cotreatment8
trichostatin Aaffects cotreatment, increases expression3
mercuric bromideincreases expression, affects cotreatment2
entinostatincreases expression, affects cotreatment2
Panobinostataffects cotreatment, increases expression2
Phenylmercuric Acetateaffects cotreatment, increases expression2
p-Chloromercuribenzoic Acidaffects cotreatment, increases expression2
GSK-J4increases expression1
methylmercuric chlorideincreases expression1
propionaldehydeincreases expression1
arseniteincreases methylation1
sodium arseniteaffects cotreatment, increases abundance, increases expression1
butyraldehydeincreases expression1
manganese chlorideaffects cotreatment, increases abundance, increases expression1
pentanalincreases expression1
perfluorooctane sulfonic aciddecreases expression1
CGP 52608increases reaction, affects binding1
4-(5-benzo(1,3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamideaffects cotreatment, increases expression1
dorsomorphinaffects cotreatment, increases expression1
incobotulinumtoxinAincreases expression1
Temozolomideincreases expression1
Vorinostatincreases expression1
Aldehydesincreases expression1
Arsenicincreases abundance, increases expression, affects cotreatment1
Calcitrioldecreases expression1
Leaddecreases expression1
Manganeseincreases abundance, increases expression, affects cotreatment1
Silicon Dioxideincreases expression1
Silverincreases expression1
Tetrachlorodibenzodioxinaffects expression1

Clinical trials (associated diseases)

0 trials via MONDO — disease-level, not drug-specific.

No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.