IER5L

gene
On this page

Also known as bA247A12.2

Summary

IER5L (immediate early response 5 like, HGNC:23679) is a protein-coding gene on chromosome 9q34.11, encoding Immediate early response gene 5-like protein (Q5T953).

At a glance

  • GWAS associations: 5
  • Clinical variants (ClinVar): 80 total
  • MANE Select transcript: NM_203434

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:23679
Approved symbolIER5L
Nameimmediate early response 5 like
Location9q34.11
Locus typegene with protein product
StatusApproved
AliasesbA247A12.2
Ensembl geneENSG00000188483
Ensembl biotypeprotein_coding
Entrez389792

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 protein_coding

ENST00000372491

RefSeq mRNA: 1 — MANE Select: NM_203434 NM_203434

CCDS: CCDS43888

Canonical transcript exons

ENST00000372491 — 1 exons

ExonStartEnd
ENSE00001457937129175552129178261

Expression profiles

Bgee: expression breadth ubiquitous, 207 present calls, max score 94.11.

FANTOM5 (CAGE): breadth ubiquitous, TPM avg 111.6698 / max 1617.1585, expressed in 1807 samples.

FANTOM5 promoters (1 alternative TSS)

Promoter IDTPM avgSamples expressed
102734111.66981807

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
kidney epitheliumUBERON:000481994.11gold quality
vena cavaUBERON:000408792.60silver quality
left ventricle myocardiumUBERON:000656690.85gold quality
descending thoracic aortaUBERON:000234590.03gold quality
cardiac muscle of right atriumUBERON:000337989.89gold quality
endocervixUBERON:000045889.51gold quality
tendon of biceps brachiiUBERON:000818888.47gold quality
ascending aortaUBERON:000149687.80gold quality
thoracic aortaUBERON:000151587.71gold quality
aortaUBERON:000094787.37gold quality
popliteal arteryUBERON:000225087.19gold quality
tibial arteryUBERON:000761087.15gold quality
pericardiumUBERON:000240787.03gold quality
deciduaUBERON:000245086.37gold quality
cortical plateUBERON:000534385.71gold quality
left coronary arteryUBERON:000162684.99gold quality
metanephros cortexUBERON:001053384.92gold quality
coronary arteryUBERON:000162184.89gold quality
tracheaUBERON:000312684.62silver quality
right coronary arteryUBERON:000162584.59gold quality
pancreatic ductal cellCL:000207984.23silver quality
peritoneumUBERON:000235883.97gold quality
omental fat padUBERON:001041483.97gold quality
ectocervixUBERON:001224983.89gold quality
left uterine tubeUBERON:000130383.60gold quality
upper arm skinUBERON:000426383.52gold quality
seminal vesicleUBERON:000099883.29gold quality
right ovaryUBERON:000211883.08gold quality
adipose tissue of abdominal regionUBERON:000780883.07gold quality
saphenous veinUBERON:000731882.95gold quality

Single-cell (SCXA)

Detected in 3 experiment(s), a significant marker in 3.

ExperimentMarker?Max mean expression
E-GEOD-135922yes21.52
E-ANND-3yes6.19
E-GEOD-137537yes6.19

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

83 targeting IER5L, 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-340-5P100.0072.504437
HSA-MIR-4476100.0068.182030
HSA-MIR-6876-5P100.0067.682126
HSA-MIR-3163100.0077.238605
HSA-MIR-1252-5P100.0069.802774
HSA-MIR-548AW99.9972.573559
HSA-MIR-513B-5P99.9969.962150
HSA-MIR-1213699.9872.815713
HSA-MIR-807599.9767.20962
HSA-MIR-3065-5P99.9771.563281
HSA-MIR-146A-5P99.9668.93988
HSA-MIR-146B-5P99.9669.13977
HSA-MIR-1468-3P99.9672.743797
HSA-MIR-4666A-3P99.9671.713434
HSA-MIR-7153-5P99.9468.891006
HSA-MIR-311999.9271.342390
HSA-MIR-338-5P99.9272.342951
HSA-MIR-6768-5P99.9267.361942
HSA-MIR-454-3P99.9174.011925
HSA-MIR-3529-3P99.9073.553045
HSA-MIR-130A-3P99.9073.311861
HSA-MIR-130B-3P99.9073.271850
HSA-MIR-301A-3P99.9073.151839
HSA-MIR-301B-3P99.9073.191836
HSA-MIR-366699.9073.241833
HSA-MIR-429599.9073.111838
HSA-MIR-95-5P99.8972.173973
HSA-MIR-182-5P99.8774.032589
HSA-MIR-477999.8666.501583
HSA-MIR-76599.8468.242442

Literature-anchored findings (GeneRIF, showing 2)

  • The results suggest that IER2, IER5, and IER5L proteins are target protein-specific regulators of PP2A (protein phosphatase 2A) activity and modulate cell proliferation through CDC25A (cell division cycle 25A protein) activity. (PMID:30599213)
  • Predictive value of immediate early response 5 like (IER5L) in the prognosis and immune checkpoint blockade therapy of non-small cell lung cancer patients. (PMID:38552564)

Cross-species orthologs

3 orthologs

OrganismSymbolGene ID
danio_rerioier5lENSDARG00000054906
mus_musculusIer5lENSMUSG00000089762
rattus_norvegicusIer5lENSRNOG00000073054

Paralogs (2): IER2 (ENSG00000160888), IER5 (ENSG00000162783)

Protein

Protein identifiers

Immediate early response gene 5-like proteinQ5T953 (reviewed: Q5T953)

All UniProt accessions (1): Q5T953

UniProt curated annotations — full annotation on UniProt →

Similarity. Belongs to the IER family.

Isoforms (2)

UniProt IDNamesCanonical?
Q5T953-11yes
Q5T953-22

RefSeq proteins (1): NP_982258* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR008653IERFamily

Pfam: PF05760

UniProt features (10 total): region of interest 3, compositionally biased region 3, splice variant 2, chain 1, sequence variant 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q5T953-F158.000.09

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 159 (showing top): E2F_Q4, E2F_Q4_01, E2F4DP1_01, GAUSSMANN_MLL_AF4_FUSION_TARGETS_C_UP, AP2_Q3, FOXO1_01, USF_C, CAGCTG_AP4_Q5, CEBP_Q2, E2F1DP1_01, E2F_Q3, E2F1DP2_01, GATA3_01, KINSEY_TARGETS_OF_EWSR1_FLII_FUSION_DN, SCHAEFFER_PROSTATE_DEVELOPMENT_6HR_DN

GO Biological Process (0):

GO Molecular Function (0):

GO Cellular Component (0):

Protein interactions and networks

STRING

450 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
IER5LSLC35F3Q8IY50425
IER5LPGM2L1Q6PCE3419
IER5LTM9SF4Q92544414
IER5LNAA25Q14CX7403
IER5LPGBD4Q96DM1402
IER5LPHAXQ9H814398
IER5LANO8Q9HCE9385
IER5LZBTB2Q8N680383
IER5LGET3O43681381
IER5LCELSR3Q9NYQ7376
IER5LRBBP8NLQ8NC74371
IER5LPUS7LQ9H0K6365
IER5LCCDC90BQ9GZT6365
IER5LYOD1Q5VVQ6360
IER5LC10orf71Q711Q0354

IntAct

6 interactions, top by confidence:

ABTypeScore
PPP2R1ASTRNpsi-mi:“MI:0914”(association)0.880
PPP2R2BMYO9Apsi-mi:“MI:0914”(association)0.640
MAPTSHTN1psi-mi:“MI:0914”(association)0.350

BioGRID (5): IER5L (Affinity Capture-RNA), IER5L (Affinity Capture-MS), IER5L (Affinity Capture-MS), IER5L (Affinity Capture-RNA), IER5L (Affinity Capture-RNA)

ESM2 similar proteins: A6NEQ2, A6NJT0, A7MB34, A8MYZ6, G3UXB3, O02755, O02756, O08934, O35392, O70218, O70220, O89113, P16443, P17542, P17676, P22091, P49716, P50548, P82976, P97830, Q00322, Q00911, Q01822, Q03484, Q10586, Q15270, Q32PF6, Q5PQP0, Q5T953, Q5TGY3, Q5VY09, Q60843, Q60925, Q64305, Q6PAL7, Q70KY4, Q7RTS3, Q80VF6, Q8WY41, Q96RK0

Diamond homologs: B7SXM5, O89113, P17950, Q5PQP0, Q5T953, Q5VY09, Q66IT9, Q6NYT3, Q6P7D3, Q6PBC9, Q99J55, Q9BTL4

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance77
Likely benign1
Benign2

Top pathogenic / likely-pathogenic (0)

SpliceAI

32 predictions. Top by Δscore:

VariantEffectΔscore
9:129176972:C:CTacceptor_gain0.5200
9:129176571:C:CCacceptor_gain0.4900
9:129176818:C:Adonor_gain0.4500
9:129176973:A:Tacceptor_gain0.4400
9:129176836:C:Adonor_gain0.4100
9:129176966:C:CTacceptor_gain0.4000
9:129176959:G:Tacceptor_gain0.3700
9:129176570:A:ACacceptor_gain0.3500
9:129176762:T:TAdonor_gain0.3200
9:129176594:G:GTacceptor_gain0.2800
9:129176595:T:TTacceptor_gain0.2800
9:129176972:C:Tacceptor_gain0.2800
9:129177127:T:TAdonor_gain0.2700
9:129176967:G:Tacceptor_gain0.2600
9:129176958:C:Tacceptor_gain0.2500
9:129176197:G:Tacceptor_gain0.2400
9:129176759:C:Adonor_gain0.2400
9:129177118:T:TAdonor_gain0.2400
9:129176569:CA:Cacceptor_gain0.2300
9:129176597:G:GTacceptor_gain0.2300
9:129177106:T:TAdonor_gain0.2300
9:129176568:TCA:Tacceptor_gain0.2200
9:129176569:CAC:Cacceptor_gain0.2200
9:129176730:AGCC:Adonor_gain0.2200
9:129177825:CG:Cdonor_gain0.2200
9:129176730:AGC:Adonor_gain0.2100
9:129176958:C:CTacceptor_gain0.2100
9:129177121:T:TAdonor_gain0.2100
9:129177147:G:Adonor_gain0.2100
9:129176570:ACTAC:Aacceptor_gain0.2000

AlphaMissense

2582 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
9:129176841:G:CF404L1.000
9:129176841:G:TF404L1.000
9:129176843:A:GF404L1.000
9:129176851:A:TI401N1.000
9:129176862:C:AW397C1.000
9:129176862:C:GW397C1.000
9:129176864:A:GW397R1.000
9:129176864:A:TW397R1.000
9:129176962:A:GF364S1.000
9:129176974:A:GF360S1.000
9:129176983:A:TI357N1.000
9:129176986:A:GL356S1.000
9:129177274:T:AD260V1.000
9:129177277:A:GL259P1.000
9:129177277:A:TL259Q1.000
9:129177280:T:AD258V1.000
9:129177280:T:CD258G1.000
9:129177283:A:GL257P1.000
9:129177926:C:GA43P1.000
9:129177931:C:GR41P1.000
9:129177934:A:GL40P1.000
9:129177934:A:TL40H1.000
9:129177949:A:GL35P1.000
9:129177952:A:GL34P1.000
9:129177952:A:TL34H1.000
9:129177954:G:CN33K1.000
9:129177954:G:TN33K1.000
9:129177957:C:AK32N1.000
9:129177957:C:GK32N1.000
9:129177958:T:AK32M1.000

dbSNP variants (sampled 300 via entrez): RS1000239133 (9:129177641 C>A,T), RS1000489864 (9:129178070 G>A,C), RS1001110391 (9:129177020 C>A), RS1001190649 (9:129178576 C>T), RS1001567367 (9:129178271 C>T), RS1002191369 (9:129179879 A>T), RS1002359485 (9:129176668 C>A,T), RS1002394632 (9:129175928 T>G), RS1002834360 (9:129175652 G>A), RS1003085922 (9:129175190 G>A), RS1003629144 (9:129175438 C>A,T), RS1003801729 (9:129176746 G>C,T), RS1004382602 (9:129177465 C>A,G), RS1004399552 (9:129177579 C>A), RS1005253633 (9:129179484 G>A)

Disease associations

OMIM: gene `` | disease phenotypes:

GenCC curated gene-disease

Mondo (0):

Orphanet (0):

HPO phenotypes

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

GWAS associations

5 associations (top):

StudyTraitp-value
GCST006624_81Systolic blood pressure1.000000e-09
GCST007432_89FEV13.000000e-09
GCST007576_129Chronotype3.000000e-11
GCST010083_77Hemoglobin levels1.000000e-09
GCST010143_23Meat-related diet6.000000e-11

EFO canonical traits (5, from GWAS)

EFO IDTrait name
EFO:0006335systolic blood pressure
EFO:0004314forced expiratory volume
EFO:0008328chronotype measurement
EFO:0004509hemoglobin measurement
EFO:0008111diet measurement

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

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

CTD chemical–gene interactions

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

ChemicalActions (top 5)PubMed papers
Valproic Acidincreases expression, increases methylation, affects expression, decreases expression5
Tetrachlorodibenzodioxinincreases expression3
(+)-JQ1 compoundincreases expression2
Benzo(a)pyreneincreases expression, increases methylation2
Estradiolaffects cotreatment, increases expression2
Ethinyl Estradiolaffects expression, increases expression2
Phenylmercuric Acetateaffects cotreatment, increases expression2
Smokeincreases abundance, decreases expression2
Tobacco Smoke Pollutionincreases expression2
aristolochic acid Idecreases expression1
methylmercuric chlorideincreases expression1
triphenyl phosphateaffects expression1
propionaldehydedecreases expression1
bisphenol Aaffects expression1
2-methyl-4-isothiazolin-3-oneincreases expression1
trichostatin Aincreases expression1
sodium arseniteaffects expression1
butyraldehydedecreases expression1
tobacco tardecreases expression1
S-(1,2-dichlorovinyl)cysteineincreases expression, affects response to substance1
cyanoginosin LRincreases expression1
di-n-butylphosphoric acidaffects expression1
4-(5-benzo(1,3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamideaffects cotreatment, increases expression1
dimethylarsinous aciddecreases expression1
abrinedecreases expression1
dorsomorphinaffects cotreatment, increases expression1
licochalcone Bincreases expression1
MT19c compounddecreases expression1
2-amino-7-(4-fluoro-2-(6-methoxypyridin-2-yl)phenyl)-4-methyl-7,8-dihydropyrido(4,3-d)pyrimidin-5(6H)-oneincreases activity, increases expression1
theaflavin-3,3’-digallateaffects 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.