LENG9

gene
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Summary

LENG9 (leukocyte receptor cluster member 9, HGNC:16306) is a protein-coding gene on chromosome 19q13.42, encoding Leukocyte receptor cluster member 9 (Q96B70).

Predicted to enable zinc ion binding activity.

Source: NCBI Gene 94059 — RefSeq curated summary.

At a glance

  • Clinical variants (ClinVar): 134 total
  • MANE Select transcript: NM_001301782

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:16306
Approved symbolLENG9
Nameleukocyte receptor cluster member 9
Location19q13.42
Locus typegene with protein product
StatusApproved
Ensembl geneENSG00000275183
Ensembl biotypeprotein_coding
Entrez94059

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 protein_coding

ENST00000611161

RefSeq mRNA: 1 — MANE Select: NM_001301782 NM_001301782

CCDS: CCDS77358

Canonical transcript exons

ENST00000611161 — 1 exons

ExonStartEnd
ENSE000037204215446173254463778

Expression profiles

Bgee: expression breadth ubiquitous, 131 present calls, max score 85.24.

FANTOM5 (CAGE): breadth ubiquitous, TPM avg 4.5170 / max 73.8720, expressed in 1582 samples.

FANTOM5 promoters (3 alternative TSS)

Promoter IDTPM avgSamples expressed
1826553.63231466
1826540.4792243
1826530.4055145

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
body of pancreasUBERON:000115085.24gold quality
mucosa of transverse colonUBERON:000499182.82gold quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099178.79silver quality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047377.52gold quality
pancreasUBERON:000126477.35gold quality
duodenumUBERON:000211475.69gold quality
apex of heartUBERON:000209875.29gold quality
body of stomachUBERON:000116174.45gold quality
lower esophagus mucosaUBERON:003583474.22gold quality
transverse colonUBERON:000115774.16gold quality
descending thoracic aortaUBERON:000234573.69gold quality
esophagus mucosaUBERON:000246973.59gold quality
thoracic aortaUBERON:000151573.38gold quality
ascending aortaUBERON:000149673.25gold quality
stromal cell of endometriumCL:000225573.15gold quality
granulocyteCL:000009473.08gold quality
minor salivary glandUBERON:000183072.42gold quality
saliva-secreting glandUBERON:000104472.38gold quality
prostate glandUBERON:000236772.35gold quality
stomachUBERON:000094572.10gold quality
left coronary arteryUBERON:000162672.06gold quality
fundus of stomachUBERON:000116071.70gold quality
esophagusUBERON:000104371.63gold quality
left adrenal glandUBERON:000123471.58gold quality
small intestineUBERON:000210871.49gold quality
bloodUBERON:000017871.48gold quality
small intestine Peyer’s patchUBERON:000345471.45gold quality
right coronary arteryUBERON:000162571.29gold quality
right adrenal glandUBERON:000123371.28gold quality
colonUBERON:000115571.21gold quality

Single-cell (SCXA)

Detected in 1 experiment(s), a significant marker in 0.

ExperimentMarker?Max mean expression
E-ANND-3no0.13

Regulation

Is transcription factor: no

Cross-species orthologs

3 orthologs

OrganismSymbolGene ID
danio_rerioleng9ENSDARG00000062374
mus_musculusLeng9ENSMUSG00000043432
rattus_norvegicusLeng9ENSRNOG00000069605

Paralogs (1): NUP42 (ENSG00000136243)

Protein

Protein identifiers

Leukocyte receptor cluster member 9Q96B70 (reviewed: Q96B70)

All UniProt accessions (1): A0A087WVD1

UniProt curated annotations — full annotation on UniProt →

RefSeq proteins (1): NP_001288711* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR000571Znf_CCCHDomain
IPR009097Cyclic_PdiesteraseHomologous_superfamily
IPR019510AKAP7-like_phosphoesteraseDomain
IPR040459MJ1316Domain
IPR042653Leng9Family

Pfam: PF00642, PF04457, PF10469

UniProt features (8 total): region of interest 4, sequence variant 2, chain 1, zinc finger region 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q96B70-F166.330.22

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 75 (showing top): AAAYRNCTG_UNKNOWN, CAGCTG_AP4_Q5, HFH4_01, E4F1_Q6, GATA4_Q3, CREBP1CJUN_01, RNCTGNYNRNCTGNY_UNKNOWN, RAY_TUMORIGENESIS_BY_ERBB2_CDC25A_DN, TEF_Q6, MARTENS_TRETINOIN_RESPONSE_DN, RP58_01, BRUINS_UVC_RESPONSE_VIA_TP53_GROUP_C, GSE14415_INDUCED_VS_NATURAL_TREG_UP, HOXA10_TARGET_GENES, ID2_TARGET_GENES

GO Biological Process (0):

GO Molecular Function (2): zinc ion binding (GO:0008270), metal ion binding (GO:0046872)

GO Cellular Component (0):

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
transition metal ion binding1
cation binding1

Protein interactions and networks

STRING

324 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
LENG9CDC42EP5Q6NZY7636
LENG9LENG8Q96PV6614
LENG9TTYH1Q9H313551
LENG9DENND10Q8TCE6425
LENG9ZC3HAV1LQ96H79420
LENG9TMCO4Q5TGY1419
LENG9PHYHIPQ92561417
LENG9ASCC1Q8N9N2417
LENG9TARM1B6A8C7413
LENG9ZMAT4Q9H898409
LENG9LENG1Q96BZ8404
LENG9GLB1L2Q8IW92391
LENG9LAIR1Q6GTX8386
LENG9C1orf159Q96HA4369
LENG9RBM26Q5T8P6363

IntAct

5 interactions, top by confidence:

ABTypeScore
CARNMT1NUP42psi-mi:“MI:0914”(association)0.640
FOXS1DDX39Apsi-mi:“MI:0914”(association)0.350
CDC5Lpsi-mi:“MI:0914”(association)0.350

BioGRID (10): LENG9 (Affinity Capture-MS), LENG9 (Affinity Capture-MS), LENG9 (Affinity Capture-MS), LENG9 (Affinity Capture-MS), LENG9 (Reconstituted Complex), LENG9 (Affinity Capture-MS), LENG9 (Affinity Capture-MS), LENG9 (Affinity Capture-MS), LENG9 (Affinity Capture-MS), LENG9 (Protein-RNA)

ESM2 similar proteins: A4GXA9, A7E3N7, A8VU90, D3KCC4, D3ZZN9, G3V8H4, O08672, O95382, Q13608, Q13671, Q14296, Q17RN3, Q28616, Q3UR50, Q3UR97, Q3V3V9, Q4KM32, Q53GL7, Q56A04, Q58CQ5, Q58EX7, Q5BK61, Q5NVA9, Q62893, Q643R3, Q66H85, Q6F5E8, Q6NVH7, Q6ZW31, Q7T0L4, Q80UU1, Q80XL1, Q8BJW7, Q8BTN6, Q8CIE4, Q8CJ00, Q8K592, Q8N2G8, Q8NAG6, Q8VCI7

Diamond homologs: O15504, Q5RB98, Q8BTN6, Q96B70

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance119
Likely benign15
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

44 predictions. Top by Δscore:

VariantEffectΔscore
19:54463492:T:TAdonor_gain0.6000
19:54462760:T:TAdonor_gain0.4400
19:54462835:C:Gacceptor_gain0.4400
19:54463133:C:CTacceptor_gain0.4300
19:54463263:G:Cdonor_gain0.4100
19:54463134:A:Cacceptor_gain0.4000
19:54463262:AGC:Adonor_gain0.3900
19:54463441:T:TAdonor_gain0.3500
19:54463006:TCGG:Tdonor_gain0.3400
19:54463007:CGGC:Cdonor_gain0.3400
19:54463048:T:TAdonor_gain0.3400
19:54462808:T:TAdonor_gain0.3300
19:54463269:C:CTdonor_gain0.3000
19:54463030:C:CAdonor_gain0.2900
19:54462765:G:Adonor_gain0.2700
19:54462809:C:Adonor_gain0.2700
19:54462954:C:CAdonor_gain0.2700
19:54462983:G:Tdonor_gain0.2700
19:54463082:C:CTacceptor_gain0.2700
19:54463266:C:CTdonor_gain0.2700
19:54462979:T:TAdonor_gain0.2600
19:54463262:AG:Adonor_gain0.2600
19:54462745:C:CAdonor_gain0.2500
19:54462922:T:TAdonor_gain0.2500
19:54463068:T:TAdonor_gain0.2500
19:54463321:T:TAdonor_gain0.2500
19:54462040:T:Adonor_gain0.2400
19:54462761:C:Adonor_gain0.2400
19:54463069:C:Adonor_gain0.2400
19:54463141:C:CTacceptor_gain0.2400

AlphaMissense

3017 scored. Top likely-pathogenic:

dbSNP variants (sampled 300 via entrez): RS1000015318 (19:54465694 G>A), RS1000128531 (19:54461898 T>C), RS1000338246 (19:54464182 C>T), RS1000481171 (19:54462022 A>G,T), RS1001362910 (19:54464228 G>A), RS1001394184 (19:54464388 G>A), RS10017 (19:54465172 C>A,T), RS1002589142 (19:54461267 G>A,C), RS1003119682 (19:54464556 C>CG), RS1003131003 (19:54464407 CTG>C), RS1003477553 (19:54463534 G>A), RS1003622646 (19:54461483 C>T), RS1003729542 (19:54465138 T>C), RS1003946265 (19:54465740 A>G), RS1004124365 (19:54465242 C>A,G)

Disease associations

OMIM: gene `` | disease phenotypes:

GenCC curated gene-disease

Mondo (1): myoepithelial tumor (MONDO:0002380)

Orphanet (0):

HPO phenotypes

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

GWAS associations

0 associations (top):

MeSH disease descriptors (1)

DescriptorNameTree numbers
D009208MyoepitheliomaC04.557.435.585

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

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

CTD chemical–gene interactions

19 total (human), top 19 by PubMed support.

ChemicalActions (top 5)PubMed papers
aristolochic acid Idecreases expression1
GSK-J4decreases expression1
aminomethylphosphonic acid (AMPA)decreases expression1
sodium arsenitedecreases expression1
ferrous chloridedecreases expression1
di-n-butylphosphoric acidaffects expression1
perfluoro-n-nonanoic acidincreases expression1
jinfukangincreases expression1
Glyphosatedecreases expression1
Air Pollutantsincreases expression, increases abundance1
Cisplatinincreases expression1
Glucosedecreases expression1
Niclosamideincreases expression1
Smokeincreases abundance, increases expression1
Urethanedecreases expression1
2,4-Dichlorophenoxyacetic Aciddecreases expression1
Cadmium Chloridedecreases expression1
Okadaic Acidincreases expression1
Lactic Acidincreases expression1

Clinical trials (associated diseases)

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

TrialPhaseStatusTitle
NCT03600649PHASE1UNKNOWNClinical Trial of SP-2577 (Seclidemstat) in Patients With Relapsed or Refractory Ewing or Ewing-related Sarcomas
NCT05266196PHASE1/PHASE2UNKNOWNA Rollover Protocol to Allow for Continued Access to the LSD1 Inhibitor Seclidemstat (SP-2577)
NCT06239272PHASE1/PHASE2RECRUITINGNRSTS2021, A Risk Adapted Study Evaluating Maintenance Pazopanib, Limited Margin, Dose-Escalated Radiation Therapy and Selinexor in Non-Rhabdomyosarcoma Soft Tissue Sarcoma (NRSTS)
NCT06625190PHASE1/PHASE2RECRUITINGAlpha/Beta T and B Cell Depletion With Zoledronic Acid for Solid Tumors
NCT06244420Not specifiedCOMPLETEDMalignant Myoepithelioma of Bone and Soft Tissues: Diagnostic Imaging and Histology in Relation to Prognosis
  • Disease cohort memberships (association, not causation — diseases whose associated-gene cohort lists this gene; a subset are also under Associated diseases): myoepithelial tumor