LGALS14

gene
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Also known as PPL13CLC2

Summary

LGALS14 (galectin 14, HGNC:30054) is a protein-coding gene on chromosome 19q13.2, encoding Placental protein 13-like (Q8TCE9). Binds beta-galactoside and lactose.

This gene is predominantly expressed in placenta. The encoded protein belongs to the galectin (galaptin/S-lectin) family. The members of galectin family contain one or two carbohydrate recognition domains, which can bind beta-galactoside. Two alternatively spliced transcript variants encoding distinct isoforms have been observed.

Source: NCBI Gene 56891 — RefSeq curated summary.

At a glance

  • GWAS associations: 1
  • Clinical variants (ClinVar): 25 total
  • MANE Select transcript: NM_020129

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:30054
Approved symbolLGALS14
Namegalectin 14
Location19q13.2
Locus typegene with protein product
StatusApproved
AliasesPPL13, CLC2
Ensembl geneENSG00000006659
Ensembl biotypeprotein_coding
OMIM607260
Entrez56891

Gene structure

Transcript identifiers

Ensembl transcripts: 3 — 3 protein_coding

ENST00000360675, ENST00000392052, ENST00000601802

RefSeq mRNA: 2 — MANE Select: NM_020129 NM_020129, NM_203471

CCDS: CCDS12542, CCDS46073

Canonical transcript exons

ENST00000392052 — 4 exons

ExonStartEnd
ENSE000003416493970717839707388
ENSE000024677613970659739706673
ENSE000030610013970919739709444
ENSE000031862633970448139704543

Expression profiles

Bgee: expression breadth broad, 59 present calls, max score 90.98.

FANTOM5 (CAGE): breadth tissue_specific, TPM avg 0.5529 / max 271.6595, expressed in 38 samples.

FANTOM5 promoters (4 alternative TSS)

Promoter IDTPM avgSamples expressed
1758040.426834
1758030.083910
1758010.027911
1758020.01437

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
placentaUBERON:000198790.98gold quality
pancreatic ductal cellCL:000207963.33silver quality
deciduaUBERON:000245062.08silver quality
tibialis anteriorUBERON:000138561.44silver quality
olfactory bulbUBERON:000226461.39gold quality
type B pancreatic cellCL:000016961.27gold quality
ileal mucosaUBERON:000033161.07gold quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099155.30gold quality
adrenal tissueUBERON:001830353.59gold quality
epithelial cell of pancreasCL:000008353.55gold quality
hair follicleUBERON:000207352.43gold quality
smooth muscle tissueUBERON:000113550.86gold quality
thymusUBERON:000237049.92gold quality
skin of hipUBERON:000155449.72silver quality
quadriceps femorisUBERON:000137749.59gold quality
Brodmann (1909) area 46UBERON:000648349.30gold quality
cervix squamous epitheliumUBERON:000692249.20gold quality
myocardiumUBERON:000234948.87gold quality
muscle tissueUBERON:000238548.76gold quality
granulocyteCL:000009448.62silver quality
cardiac muscle of right atriumUBERON:000337948.55gold quality
CA1 field of hippocampusUBERON:000388148.50gold quality
cervix epitheliumUBERON:000480148.44gold quality
vastus lateralisUBERON:000137948.25gold quality
left ventricle myocardiumUBERON:000656648.24gold quality
oviduct epitheliumUBERON:000480448.21gold quality
orbitofrontal cortexUBERON:000416748.20gold quality
upper arm skinUBERON:000426348.06gold quality
tongue squamous epitheliumUBERON:000691947.92gold quality
mucosa of urinary bladderUBERON:000125947.80gold quality

Single-cell (SCXA)

Detected in 1 experiment(s), a significant marker in 1.

ExperimentMarker?Max mean expression
E-ANND-3yes2.78

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

9 targeting LGALS14, 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-6513-3P99.5969.771102
HSA-MIR-580-5P99.2870.941776
HSA-MIR-670-3P99.0368.882404
HSA-MIR-4650-3P99.0168.391062
HSA-MIR-4778-5P97.9668.061634
HSA-MIR-6783-5P97.6767.211528
HSA-MIR-468996.9765.791209
HSA-MIR-6782-5P96.4564.42612
HSA-MIR-6858-5P96.0564.591020

Literature-anchored findings (GeneRIF, showing 3)

  • cloning and expression in placenta - base sequence and amino acid sequences are given (PMID:11997112)
  • CIC-2 siRNA could inhibit the cell proliferation of a human glioma cell line U-87. (PMID:16831268)
  • Structure-function studies of galectin-14, an important effector molecule in embryology. (PMID:32525264)

Cross-species orthologs

31 orthologs

OrganismSymbolGene ID
danio_reriolgals9l1ENSDARG00000025903
danio_reriolgals9l3ENSDARG00000041060
danio_reriolgals3bENSDARG00000044001
danio_reriosi:ch211-10a23.2ENSDARG00000060656
danio_reriolgals9l4ENSDARG00000069058
danio_reriolgals9l5ENSDARG00000087311
danio_reriosi:dkey-95h12.2ENSDARG00000092923
danio_reriolgals9l6ENSDARG00000093059
mus_musculusLgals9ENSMUSG00000001123
rattus_norvegicusLgals5ENSRNOG00000012557
rattus_norvegicusLgals9ENSRNOG00000012681
drosophila_melanogastergalectinFBGN0031213
drosophila_melanogasterCG11374FBGN0031214
drosophila_melanogasterCG13950FBGN0031289
caenorhabditis_elegansWBGENE00002264
caenorhabditis_elegansWBGENE00002266
caenorhabditis_elegansWBGENE00002269
caenorhabditis_elegansWBGENE00002270
caenorhabditis_elegansWBGENE00002271
caenorhabditis_elegansWBGENE00004165
caenorhabditis_elegansC27C7.5WBGENE00007768
caenorhabditis_elegansF46A8.3WBGENE00009746
caenorhabditis_elegansF46A8.4WBGENE00009747
caenorhabditis_elegansF46A8.5WBGENE00009748
caenorhabditis_elegansF46A8.8WBGENE00009751
caenorhabditis_elegansWBGENE00017080
caenorhabditis_elegansWBGENE00018255
caenorhabditis_elegansWBGENE00018649
caenorhabditis_elegansWBGENE00018650
caenorhabditis_elegansWBGENE00018651
caenorhabditis_elegansWBGENE00235368

Paralogs (16): LGALS2 (ENSG00000100079), LGALS1 (ENSG00000100097), LGALS13 (ENSG00000105198), CLC (ENSG00000105205), LGALS8 (ENSG00000116977), LGALSL (ENSG00000119862), LGALS3 (ENSG00000131981), LGALS12 (ENSG00000133317), LGALS9 (ENSG00000168961), LGALS9B (ENSG00000170298), LGALS4 (ENSG00000171747), LGALS9C (ENSG00000171916), LGALS7B (ENSG00000178934), LGALS7 (ENSG00000205076), LGALS16 (ENSG00000249861), GRIFIN (ENSG00000275572)

Protein

Protein identifiers

Placental protein 13-likeQ8TCE9 (reviewed: Q8TCE9)

Alternative names: Charcot-Leyden crystal protein 2, Galectin-14

All UniProt accessions (2): Q8TCE9, M0R163

UniProt curated annotations — full annotation on UniProt →

Function. Binds beta-galactoside and lactose. Strong inducer of T-cell apoptosis.

Subcellular location. Nucleus.

Tissue specificity. Highly expressed in placenta.

Isoforms (2)

UniProt IDNamesCanonical?
Q8TCE9-11yes
Q8TCE9-22

RefSeq proteins (2): NP_064514, NP_982297 (=MANE)

Domains & families (InterPro)

IDNameType
IPR001079Galectin_CRDDomain
IPR013320ConA-like_dom_sfHomologous_superfamily
IPR044156Galectin-likeFamily

Pfam: PF00337

UniProt features (18 total): strand 10, sequence variant 2, sequence conflict 2, chain 1, domain 1, helix 1, splice variant 1

Structure

Experimental structures (PDB)

2 structures.

PDBMethodResolution (Å)
6K2YX-RAY DIFFRACTION1.57
6K2ZX-RAY DIFFRACTION2

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q8TCE9-F197.270.98

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 38 (showing top): XU_HGF_TARGETS_REPRESSED_BY_AKT1_DN, BLALOCK_ALZHEIMERS_DISEASE_UP, GNF2_KISS1, KUUSELO_PANCREATIC_CANCER_19Q13_AMPLIFICATION, GNF2_TIMP2, KRIGE_RESPONSE_TO_TOSEDOSTAT_6HR_DN, PURBEY_TARGETS_OF_CTBP1_NOT_SATB1_UP, KRAS.600_UP.V1_UP, KRAS.600.LUNG.BREAST_UP.V1_UP, SKIL_TARGET_GENES, ZNF146_TARGET_GENES, GSE10325_MYELOID_VS_LUPUS_MYELOID_UP, MIR6513_3P, GSE13411_NAIVE_VS_IGM_MEMORY_BCELL_UP, GSE13485_CTRL_VS_DAY1_YF17D_VACCINE_PBMC_DN

GO Biological Process (1): apoptotic process (GO:0006915)

GO Molecular Function (2): carbohydrate binding (GO:0030246), protein binding (GO:0005515)

GO Cellular Component (2): nucleoplasm (GO:0005654), nucleus (GO:0005634)

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
binding2
programmed cell death1
apoptotic signaling pathway1
execution phase of apoptosis1
nuclear lumen1
cellular anatomical structure1
intracellular membrane-bounded organelle1

Protein interactions and networks

STRING

280 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
LGALS14LGALS1P09382564
LGALS14LGALS2P05162507
LGALS14ITLN2Q8WWU7474
LGALS14APOL4Q9BPW4449
LGALS14LGALS4P56470367
LGALS14GCM1Q9NP62348
LGALS14CGB5P01233348
LGALS14PAPPAQ13219325
LGALS14ERVV-2B6SEH9325
LGALS14PAPPA2Q9BXP8323
LGALS14ERVV-1B6SEH8313
LGALS14A6NFB4A6NFB4305
LGALS14LGALSLQ3ZCW2301
LGALS14ZBED10PQ96FA7297
LGALS14ZNF846Q147U1296

IntAct

195 interactions, top by confidence:

ABTypeScore
GFAPLGALS14psi-mi:“MI:0915”(physical association)0.780
IKZF3LGALS14psi-mi:“MI:0915”(physical association)0.780
LGALS14IKZF3psi-mi:“MI:0915”(physical association)0.780
LGALS14GFAPpsi-mi:“MI:0915”(physical association)0.780
TRIM27LGALS14psi-mi:“MI:0915”(physical association)0.720
LGALS14FLNApsi-mi:“MI:0915”(physical association)0.720
LGALS14CRLF3psi-mi:“MI:0915”(physical association)0.720
SPAG5LGALS14psi-mi:“MI:0915”(physical association)0.720
MID2LGALS14psi-mi:“MI:0915”(physical association)0.720
LGALS14TRIM27psi-mi:“MI:0915”(physical association)0.720
FLNALGALS14psi-mi:“MI:0915”(physical association)0.720
CRLF3LGALS14psi-mi:“MI:0915”(physical association)0.720
LGALS14MID2psi-mi:“MI:0915”(physical association)0.720
LGALS14SPAG5psi-mi:“MI:0915”(physical association)0.720

BioGRID (60): LGALS14 (Two-hybrid), LGALS14 (Two-hybrid), LGALS14 (Two-hybrid), LGALS14 (Two-hybrid), LGALS14 (Two-hybrid), LGALS14 (Two-hybrid), LGALS14 (Two-hybrid), LGALS14 (Two-hybrid), LGALS14 (Two-hybrid), LGALS14 (Two-hybrid), LGALS14 (Two-hybrid), LGALS14 (Two-hybrid), LGALS14 (Two-hybrid), LGALS14 (Two-hybrid), LNX1 (Two-hybrid)

ESM2 similar proteins: A0A3Q1N1R0, A4D1Z8, A8MUM7, D3ZGS3, O00214, O08573, O14727, O23547, O44126, O54891, O88644, O88879, P07583, P08520, P11762, P23668, P26788, P36573, P38552, P47967, P56180, P56217, P56470, P79238, P97400, P97840, Q01968, Q05315, Q09581, Q09605, Q29058, Q3MHZ8, Q62665, Q6DGJ1, Q6NVF0, Q801X7, Q8C726, Q8K419, Q8LEV3, Q8TCE9

Diamond homologs: A8MUM7, O00182, O08573, O54891, P38486, P38552, P47929, P79238, P97400, P97840, Q05315, Q29058, Q3B8N2, Q3MHZ8, Q3T0D6, Q6DKI2, Q8K419, Q8TCE9, Q9UHV8, A4D1Z8, O00214, O44126, O54974, O88644, P07583, P08520, P08699, P16110, P17931, P23668, P47845, P47953, P47967, P56217, P56470, P97590, Q09605, Q09610, Q1ECW6, Q29373

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance24
Likely benign0
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

537 predictions. Top by Δscore:

VariantEffectΔscore
19:39704544:G:GGdonor_gain1.0000
19:39707176:A:AGacceptor_gain1.0000
19:39707177:G:GGacceptor_gain1.0000
19:39707177:GCAA:Gacceptor_gain1.0000
19:39709191:TTGTA:Tacceptor_loss1.0000
19:39709192:TGTA:Tacceptor_loss1.0000
19:39709193:GTA:Gacceptor_loss1.0000
19:39709194:TA:Tacceptor_loss1.0000
19:39709195:A:Tacceptor_loss1.0000
19:39709196:GGTA:Gacceptor_gain1.0000
19:39704521:A:Tdonor_gain0.9900
19:39704539:TACCC:Tdonor_gain0.9900
19:39704540:ACCC:Adonor_gain0.9900
19:39704541:CCC:Cdonor_gain0.9900
19:39704542:CC:Cdonor_gain0.9900
19:39704543:CG:Cdonor_loss0.9900
19:39704544:G:GCdonor_loss0.9900
19:39704545:T:TCdonor_loss0.9900
19:39704546:GA:Gdonor_loss0.9900
19:39704547:A:ACdonor_loss0.9900
19:39707174:TCA:Tacceptor_loss0.9900
19:39707177:GC:Gacceptor_gain0.9900
19:39707248:C:CAacceptor_gain0.9900
19:39707255:ACTTT:Aacceptor_gain0.9900
19:39707259:T:TAacceptor_gain0.9900
19:39707385:CAAG:Cdonor_gain0.9900
19:39707385:CAAGG:Cdonor_loss0.9900
19:39707386:AAGGT:Adonor_loss0.9900
19:39707387:AG:Adonor_gain0.9900
19:39707388:GG:Gdonor_gain0.9900

AlphaMissense

909 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
19:39709227:T:CF112L0.944
19:39709229:T:AF112L0.944
19:39709229:T:GF112L0.944
19:39707350:T:CF89L0.915
19:39707352:T:AF89L0.915
19:39707352:T:GF89L0.915
19:39707239:T:CF52L0.892
19:39707241:C:AF52L0.892
19:39707241:C:GF52L0.892
19:39706651:G:TG24W0.873
19:39707384:A:CY100S0.865
19:39707257:T:CF58L0.852
19:39707259:T:AF58L0.852
19:39707259:T:GF58L0.852
19:39707240:T:CF52S0.846
19:39706646:T:GI22S0.844
19:39706646:T:AI22N0.843
19:39707383:T:CY100H0.839
19:39707332:T:CF83L0.828
19:39707334:T:AF83L0.828
19:39707334:T:GF83L0.828
19:39706646:T:CI22T0.820
19:39707246:T:CF54S0.819
19:39707203:T:CF40L0.809
19:39707205:C:AF40L0.809
19:39707205:C:GF40L0.809
19:39706640:T:AV20E0.808
19:39707204:T:CF40S0.805
19:39707281:A:CS66R0.800
19:39707283:T:AS66R0.800

dbSNP variants (sampled 300 via entrez): RS1000685691 (19:39708026 T>A), RS1000704593 (19:39707772 C>G), RS1001013504 (19:39704745 C>A,T), RS1001219566 (19:39709578 A>G), RS1002085547 (19:39704801 A>C), RS1002162946 (19:39708674 T>C,G), RS1002442612 (19:39708944 G>A,T), RS1002498144 (19:39709825 A>G), RS1003111172 (19:39706329 A>G), RS1004323780 (19:39708637 G>A), RS1004354944 (19:39708896 G>T), RS1004604038 (19:39707045 A>T), RS1004705755 (19:39709813 T>C,G), RS1004881669 (19:39704115 T>C), RS1005572677 (19:39708228 G>A)

Disease associations

OMIM: gene MIM:607260 | disease phenotypes:

GenCC curated gene-disease

Mondo (0):

Orphanet (0):

HPO phenotypes

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

GWAS associations

1 associations (top):

StudyTraitp-value
GCST004624_20Sum eosinophil basophil counts1.000000e-44

EFO canonical traits (2, from GWAS)

EFO IDTrait name
EFO:0004842eosinophil count
EFO:0005090basophil count

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

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

CTD chemical–gene interactions

8 total (human), top 8 by PubMed support.

ChemicalActions (top 5)PubMed papers
beauvericinaffects cotreatment, increases expression1
enniatinsaffects cotreatment, increases expression1
Arbutindecreases expression1
Benzo(a)pyreneincreases methylation1
Diethylhexyl Phthalateincreases expression1
Pesticidesincreases expression1
Tetrachlorodibenzodioxinincreases expression1
beta-Naphthoflavonedecreases 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.