ACTR3C

gene
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Also known as ARP11

Summary

ACTR3C (actin related protein 3C, HGNC:37282) is a protein-coding gene on chromosome 7q36.1, encoding Actin-related protein 3C (Q9C0K3). May play a role in the suppression of metastatic potential in lung adenoma carcinoma cells.

Predicted to enable ATP binding activity and actin binding activity. Predicted to contribute to actin filament binding activity. Located in extracellular exosome.

Source: NCBI Gene 653857 — RefSeq curated summary.

At a glance

  • GWAS associations: 1
  • Clinical variants (ClinVar): 45 total — 2 pathogenic
  • MANE Select transcript: NM_001164458

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:37282
Approved symbolACTR3C
Nameactin related protein 3C
Location7q36.1
Locus typegene with protein product
StatusApproved
AliasesARP11
Ensembl geneENSG00000106526
Ensembl biotypeprotein_coding
Entrez653857

Gene structure

Transcript identifiers

Ensembl transcripts: 25 — 25 protein_coding

ENST00000252071, ENST00000477367, ENST00000477871, ENST00000478393, ENST00000539352, ENST00000683684, ENST00000865059, ENST00000865060, ENST00000865061, ENST00000865062, ENST00000865063, ENST00000865064, ENST00000865065, ENST00000865066, ENST00000865067, ENST00000865068, ENST00000865069, ENST00000865070, ENST00000916821, ENST00000944427, ENST00000944428, ENST00000944429, ENST00000944430, ENST00000944431, ENST00000944432

RefSeq mRNA: 2 — MANE Select: NM_001164458 NM_001164458, NM_001164459

CCDS: CCDS47744

Canonical transcript exons

ENST00000683684 — 8 exons

ExonStartEnd
ENSE00001403670150248948150249054
ENSE00002468905150286367150286540
ENSE00002491228150284753150284845
ENSE00002512088150289450150289593
ENSE00003665482150295252150295347
ENSE00003786250150293312150293419
ENSE00003918085150323469150323545
ENSE00003918770150247212150247569

Expression profiles

Bgee: expression breadth ubiquitous, 173 present calls, max score 85.11.

FANTOM5 (CAGE): breadth ubiquitous, TPM avg 3.2429 / max 60.4568, expressed in 921 samples.

FANTOM5 promoters (6 alternative TSS)

Promoter IDTPM avgSamples expressed
867692.0879736
867700.5533262
867680.3971207
867710.159173
867670.031114
2049980.01425

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
right lobe of liverUBERON:000111485.11gold quality
liverUBERON:000210781.74gold quality
islet of LangerhansUBERON:000000681.58gold quality
body of pancreasUBERON:000115081.41gold quality
right adrenal gland cortexUBERON:003582781.22gold quality
left adrenal gland cortexUBERON:003582580.94gold quality
right adrenal glandUBERON:000123380.56gold quality
pancreasUBERON:000126480.37gold quality
left adrenal glandUBERON:000123480.26gold quality
metanephros cortexUBERON:001053379.78gold quality
adult mammalian kidneyUBERON:000008279.61gold quality
adrenal cortexUBERON:000123579.53gold quality
adrenal glandUBERON:000236979.26gold quality
kidney epitheliumUBERON:000481978.87gold quality
rectumUBERON:000105277.74gold quality
bone marrow cellCL:000209277.09gold quality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047376.01gold quality
esophagus mucosaUBERON:000246975.28gold quality
kidneyUBERON:000211375.22gold quality
olfactory segment of nasal mucosaUBERON:000538675.12gold quality
adrenal tissueUBERON:001830374.94gold quality
cortex of kidneyUBERON:000122574.08gold quality
mucosa of transverse colonUBERON:000499173.94gold quality
gall bladderUBERON:000211073.36gold quality
oviduct epitheliumUBERON:000480473.18gold quality
adenohypophysisUBERON:000219672.90gold quality
body of stomachUBERON:000116172.45gold quality
pituitary glandUBERON:000000772.28gold quality
minor salivary glandUBERON:000183071.87gold quality
colonic epitheliumUBERON:000039771.83gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3yes6.33

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

41 targeting ACTR3C, 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-30A-5P100.0076.313233
HSA-MIR-30B-5P100.0076.293248
HSA-MIR-30C-5P100.0076.293248
HSA-MIR-30D-5P100.0076.323233
HSA-MIR-30E-5P100.0076.323242
HSA-LET-7A-3P100.0074.033932
HSA-LET-7B-3P100.0074.083913
HSA-LET-7F-1-3P100.0074.023928
HSA-MIR-98-3P100.0074.083907
HSA-MIR-7110-3P100.0073.182486
HSA-MIR-607799.9968.042299
HSA-MIR-4715-3P99.9866.03670
HSA-MIR-520D-5P99.9873.344883
HSA-MIR-524-5P99.9873.434882
HSA-MIR-515-5P99.9269.822343
HSA-MIR-519E-5P99.9269.622358
HSA-MIR-6892-3P99.6866.401178
HSA-MIR-580-3P99.6769.231841
HSA-MIR-443799.5265.291266
HSA-MIR-216A-5P99.5068.021288
HSA-MIR-7849-3P99.4768.171224
HSA-MIR-122B-5P99.4670.811457
HSA-MIR-372-5P99.4169.112299
HSA-MIR-569599.4167.481047
HSA-MIR-6731-5P99.2867.422375
HSA-MIR-808599.2867.562362
HSA-MIR-472199.2666.05818
HSA-MIR-3925-5P99.2167.901466
HSA-MIR-4758-3P99.1263.96869
HSA-MIR-10524-5P99.0566.08963

Cross-species orthologs

3 orthologs

OrganismSymbolGene ID
danio_rerioactr3bENSDARG00000008790
mus_musculusActr3bENSMUSG00000056367
rattus_norvegicusActr3bENSRNOG00000031855

Paralogs (26): ACTR6 (ENSG00000075089), ACTB (ENSG00000075624), ACTL6B (ENSG00000077080), ACTR5 (ENSG00000101442), ACTA2 (ENSG00000107796), ACTR8 (ENSG00000113812), ACTR1B (ENSG00000115073), ACTR3 (ENSG00000115091), ACTL8 (ENSG00000117148), ACTRT1 (ENSG00000123165), ACTR10 (ENSG00000131966), ACTR3B (ENSG00000133627), ACTL6A (ENSG00000136518), ACTR2 (ENSG00000138071), ACTR1A (ENSG00000138107), ACTA1 (ENSG00000143632), ACTL7B (ENSG00000148156), ACTC1 (ENSG00000159251), ACTG2 (ENSG00000163017), ACTBL2 (ENSG00000169067), ACTRT2 (ENSG00000169717), ACTL9 (ENSG00000181786), ACTG1 (ENSG00000184009), ACTRT3 (ENSG00000184378), ACTL7A (ENSG00000187003), ACTL10 (ENSG00000288649)

Protein

Protein identifiers

Actin-related protein 3CQ9C0K3 (reviewed: Q9C0K3)

Alternative names: Actin-related protein 11

All UniProt accessions (5): Q9C0K3, A0A0A0MTI9, C9IZN3, C9J580, H7C4J1

UniProt curated annotations — full annotation on UniProt →

Function. May play a role in the suppression of metastatic potential in lung adenoma carcinoma cells.

Tissue specificity. Expressed in kidney, stomach, spleen, bone marrow, uterus, testis, placenta, skeletal muscle, mammary gland, lung, fetal liver, and fetal kidney, but not detected in small intestine, brain, and thymus. Expressed in low-metastatic lung adenocarcinoma cells but not in high-metastatic ones.

Similarity. Belongs to the actin family.

Isoforms (2)

UniProt IDNamesCanonical?
Q9C0K3-11yes
Q9C0K3-22

RefSeq proteins (2): NP_001157930, NP_001157931 (=MANE)

Domains & families (InterPro)

IDNameType
IPR004000ActinFamily
IPR043129ATPase_NBDHomologous_superfamily

Pfam: PF00022

UniProt features (4 total): signal peptide 1, chain 1, splice variant 1, sequence conflict 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q9C0K3-F187.320.78

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 50 (showing top): GOMF_ACTIN_BINDING, GRYDER_PAX3FOXO1_ENHANCERS_IN_TADS, GOMF_CYTOSKELETAL_PROTEIN_BINDING, GOMF_ADENYL_NUCLEOTIDE_BINDING, GRYDER_PAX3FOXO1_ENHANCERS_KO_DOWN, ATF6_TARGET_GENES, FOXJ2_TARGET_GENES, FOXN3_TARGET_GENES, H1_6_TARGET_GENES, HOXB4_TARGET_GENES, HOXC6_TARGET_GENES, MAFG_TARGET_GENES, MEF2D_TARGET_GENES, NFE2L1_TARGET_GENES, NKX2_3_TARGET_GENES

GO Biological Process (0):

GO Molecular Function (4): actin binding (GO:0003779), ATP binding (GO:0005524), nucleotide binding (GO:0000166), actin filament binding (GO:0051015)

GO Cellular Component (1): extracellular exosome (GO:0070062)

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
cytoskeletal protein binding1
adenyl ribonucleotide binding1
purine ribonucleoside triphosphate binding1
nucleoside phosphate binding1
heterocyclic compound binding1
actin binding1
protein-containing complex binding1
extracellular vesicle1

Protein interactions and networks

STRING

2027 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
ACTR3CACTR2P61160976
ACTR3CDCTN2Q13561912
ACTR3CDCTN4Q9UJW0864
ACTR3CDCTN5Q9BTE1858
ACTR3CTPPPO94811847
ACTR3CCAPZA2P47755822
ACTR3CCAPZA1P52907808
ACTR3CDCTN6O00399803
ACTR3CDCTN1Q14203799
ACTR3CARPC2O15144712
ACTR3CARPC5O15511706
ACTR3CARPC3O15145686
ACTR3CACTBP02570678
ACTR3CWASP42768588
ACTR3CLRRC61Q9BV99584

IntAct

8 interactions, top by confidence:

ABTypeScore
STN1SMCO3psi-mi:“MI:0914”(association)0.530
ITGB8GET1psi-mi:“MI:0914”(association)0.530
DUSP21A2ML1psi-mi:“MI:0914”(association)0.350
DND1ATXN3psi-mi:“MI:0914”(association)0.350
MALLGPR89Apsi-mi:“MI:0914”(association)0.350
HCRTR2FADS1psi-mi:“MI:0914”(association)0.350

BioGRID (12): ACTR3C (Affinity Capture-MS), ACTR3C (Affinity Capture-MS), ACTR3C (Affinity Capture-MS), ACTR3C (Affinity Capture-MS), ACTR3C (Affinity Capture-MS), ACTR3C (Affinity Capture-MS), ACTR3C (Affinity Capture-RNA), ACTR3C (Affinity Capture-MS), ACTR3C (Affinity Capture-MS), ACTR3C (Affinity Capture-MS), ACTR3C (Affinity Capture-MS), ACTR3C (Affinity Capture-MS)

ESM2 similar proteins: A0A1L8EV45, C9WPN6, F1QGW6, F6RQL9, O73723, O77676, P00516, P0C605, P20461, P23258, P23330, P31321, P32392, P35250, P41091, P53033, P61157, P61158, P62482, P62483, P81795, P83887, P83888, Q05B83, Q0VCD2, Q13126, Q13303, Q13976, Q27955, Q2KHU8, Q2KJ81, Q2VIR3, Q32KM1, Q4V7C7, Q5R797, Q5R8R1, Q5ZHS1, Q5ZMS3, Q641P0, Q641W4

Diamond homologs: A0A1L8EV45, A2BDB0, A2X6S3, O16808, O17320, O18840, O73723, P02576, P02578, P04752, P04829, P07829, P0DM41, P0DM42, P10984, P10986, P10988, P10990, P12716, P13363, P17126, P17128, P22132, P26183, P27131, P30162, P30163, P32390, P32392, P35432, P41112, P41339, P42528, P43239, P45886, P47117, P53458, P53461, P53468, P53470

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic2
Likely pathogenic0
Uncertain significance35
Likely benign0
Benign2

Top pathogenic / likely-pathogenic (2)

Variant IDHGVSClassification
3391897GRCh37/hg19 7q31.32-36.1(chr7:122190535-149944340)x1Pathogenic
57185GRCh38/hg38 7q35-36.1(chr7:147345844-150426340)x1Pathogenic

SpliceAI

2316 predictions. Top by Δscore:

VariantEffectΔscore
7:150284842:CAAA:Cacceptor_gain1.0000
7:150284846:C:CCacceptor_gain1.0000
7:150284851:T:Cacceptor_gain1.0000
7:150284851:T:TCacceptor_gain1.0000
7:150284853:G:Cacceptor_gain1.0000
7:150284853:G:GCacceptor_gain1.0000
7:150284855:A:ACacceptor_gain1.0000
7:150284855:A:Cacceptor_gain1.0000
7:150284859:CAA:Cacceptor_gain1.0000
7:150284860:A:Tacceptor_gain1.0000
7:150284861:A:ACacceptor_gain1.0000
7:150284861:A:Cacceptor_gain1.0000
7:150284863:A:Cacceptor_gain1.0000
7:150286361:CCTTA:Cdonor_loss1.0000
7:150286362:CTTA:Cdonor_loss1.0000
7:150286363:TTA:Tdonor_loss1.0000
7:150286364:TA:Tdonor_loss1.0000
7:150286365:A:ATdonor_loss1.0000
7:150286365:ACCT:Adonor_gain1.0000
7:150286366:C:CGdonor_loss1.0000
7:150286366:CCT:Cdonor_gain1.0000
7:150286366:CCTC:Cdonor_gain1.0000
7:150295246:TTTTA:Tdonor_loss1.0000
7:150295247:TTTA:Tdonor_loss1.0000
7:150295248:TTA:Tdonor_loss1.0000
7:150295249:TA:Tdonor_loss1.0000
7:150295250:A:AGdonor_loss1.0000
7:150295251:CCTG:Cdonor_loss1.0000
7:150295344:CTGT:Cacceptor_gain1.0000
7:150295346:GTCT:Gacceptor_loss1.0000

AlphaMissense

0 scored. Top likely-pathogenic:

dbSNP variants (sampled 300 via entrez): RS1000002215 (7:150127353 C>G), RS1000014160 (7:150032693 C>A), RS1000027285 (7:150278144 G>A,T), RS1000028133 (7:150230241 A>C), RS1000030712 (7:150174702 C>A,G), RS1000045177 (7:150032538 C>T), RS1000049177 (7:149981999 A>G), RS1000051010 (7:150082634 C>A), RS1000052030 (7:149882416 C>T), RS1000063409 (7:150324086 G>T), RS1000072646 (7:149886488 C>T), RS1000119052 (7:150084128 T>G), RS1000120777 (7:149937584 C>T), RS1000135859 (7:149989072 C>T), RS1000142761 (7:150277993 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

1 associations (top):

StudyTraitp-value
GCST004389_3Circulating chemerin levels8.000000e-14

EFO canonical traits (1, from GWAS)

EFO IDTrait name
EFO:0004573chemerin measurement

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

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

CTD chemical–gene interactions

20 total (human), top 20 by PubMed support.

ChemicalActions (top 5)PubMed papers
Benzo(a)pyreneaffects methylation, decreases methylation2
Cadmium Chloridedecreases expression, increases expression2
aristolochic acid Idecreases expression1
triphenyl phosphateaffects expression1
ethyl-p-hydroxybenzoateincreases expression1
tris(2-butoxyethyl) phosphateaffects expression1
beta-lapachoneincreases expression1
butyraldehydedecreases expression1
benzo(e)pyreneincreases methylation1
aflatoxin B2decreases methylation1
cupric oxidedecreases expression1
Arsenic Trioxideincreases expression1
Acetaminophendecreases expression1
Estradiolaffects cotreatment, decreases expression1
Methapyrileneincreases methylation1
Tobacco Smoke Pollutiondecreases expression1
Tretinoindecreases expression1
Valproic Aciddecreases expression1
Cyclosporinedecreases expression1
Aflatoxin B1increases methylation1

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.