FNDC10

gene
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Summary

FNDC10 (fibronectin type III domain containing 10, HGNC:42951) is a protein-coding gene on chromosome 1p36.33, encoding Fibronectin type III domain-containing protein 10 (F2Z333).

Predicted to be located in membrane.

Source: NCBI Gene 643988 — RefSeq curated summary.

At a glance

  • GWAS associations: 1
  • Clinical variants (ClinVar): 2 total — 1 pathogenic
  • Phenotypes (HPO): 1
  • MANE Select transcript: NM_001242659

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:42951
Approved symbolFNDC10
Namefibronectin type III domain containing 10
Location1p36.33
Locus typegene with protein product
StatusApproved
Ensembl geneENSG00000228594
Ensembl biotypeprotein_coding
Entrez643988

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 protein_coding

ENST00000422725

RefSeq mRNA: 1 — MANE Select: NM_001242659 NM_001242659

CCDS: CCDS55559

Canonical transcript exons

ENST00000422725 — 1 exons

ExonStartEnd
ENSE0000179273715980121600135

Expression profiles

Bgee: expression breadth ubiquitous, 191 present calls, max score 89.91.

FANTOM5 (CAGE): breadth ubiquitous, TPM avg 2.8952 / max 40.9479, expressed in 1131 samples.

FANTOM5 promoters (3 alternative TSS)

Promoter IDTPM avgSamples expressed
98072.1223973
98060.5972303
98050.175797

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
pancreatic ductal cellCL:000207989.91silver quality
right adrenal gland cortexUBERON:003582787.55gold quality
right adrenal glandUBERON:000123387.16gold quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099186.74gold quality
left adrenal gland cortexUBERON:003582586.69gold quality
left adrenal glandUBERON:000123486.26gold quality
hypothalamusUBERON:000189886.01gold quality
adrenal cortexUBERON:000123585.75gold quality
right frontal lobeUBERON:000281085.74gold quality
anterior cingulate cortexUBERON:000983585.30gold quality
Brodmann (1909) area 9UBERON:001354083.64gold quality
adrenal glandUBERON:000236983.31gold quality
dorsolateral prefrontal cortexUBERON:000983483.04gold quality
amygdalaUBERON:000187682.36gold quality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047381.85gold quality
apex of heartUBERON:000209881.09gold quality
tibialis anteriorUBERON:000138580.93silver quality
stromal cell of endometriumCL:000225580.32gold quality
ileal mucosaUBERON:000033180.15gold quality
neocortexUBERON:000195080.15gold quality
cerebral cortexUBERON:000095679.98gold quality
Ammon’s hornUBERON:000195479.60gold quality
frontal cortexUBERON:000187079.37gold quality
primary visual cortexUBERON:000243679.34gold quality
C1 segment of cervical spinal cordUBERON:000646979.32gold quality
nucleus accumbensUBERON:000188279.26gold quality
substantia nigraUBERON:000203879.11gold quality
forebrainUBERON:000189078.95gold quality
temporal lobeUBERON:000187178.70gold quality
kidney epitheliumUBERON:000481978.61gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3yes3.44

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

45 targeting FNDC10, 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-3134100.0066.43777
HSA-MIR-453499.9966.581907
HSA-MIR-118499.9968.191458
HSA-MIR-4715-3P99.9866.03670
HSA-MIR-808299.9567.271170
HSA-MIR-4731-5P99.8967.232537
HSA-MIR-124-3P99.8973.743043
HSA-MIR-506-3P99.8973.553057
HSA-MIR-10395-5P99.8667.35676
HSA-MIR-6875-3P99.8270.262983
HSA-MIR-518A-5P99.7069.012209
HSA-MIR-52799.7069.012209
HSA-MIR-10394-5P99.6566.831852
HSA-MIR-120599.6566.761826
HSA-MIR-425199.4069.193363
HSA-MIR-4685-5P99.2565.991563
HSA-MIR-6837-5P99.2565.471632
HSA-MIR-478499.1567.411733
HSA-MIR-6768-3P99.1467.381319
HSA-MIR-465199.0667.572002
HSA-MIR-3619-5P99.0068.872308
HSA-MIR-60898.9367.832013
HSA-MIR-3150B-3P98.8167.211728
HSA-MIR-76098.8166.651392
HSA-MIR-331-3P98.7664.91793
HSA-MIR-6761-5P98.7168.031504
HSA-MIR-214-3P98.7168.122128
HSA-MIR-6804-5P98.3965.771084
HSA-MIR-4704-3P98.2869.331300
HSA-MIR-4664-5P98.1765.071020

Cross-species orthologs

3 orthologs

OrganismSymbolGene ID
danio_reriofndc10ENSDARG00000078657
mus_musculusFndc10ENSMUSG00000074738
rattus_norvegicusRps15al2ENSRNOG00000030447

Protein

Protein identifiers

Fibronectin type III domain-containing protein 10F2Z333 (reviewed: F2Z333)

All UniProt accessions (1): F2Z333

UniProt curated annotations — full annotation on UniProt →

Subcellular location. Membrane.

RefSeq proteins (1): NP_001229588* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR034446Fndc10Family

Pfam: PF17742

UniProt features (8 total): topological domain 2, glycosylation site 2, signal peptide 1, chain 1, transmembrane region 1, domain 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-F2Z333-F177.510.38

Functional residue map

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

Glycosylation sites (2): 86, 109

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 36 (showing top): GSE45365_CTRL_VS_MCMV_INFECTION_NK_CELL_UP, chr1p36, GSE13522_CTRL_VS_T_CRUZI_Y_STRAIN_INF_SKIN_IFNAR_KO_UP, ZNF563_TARGET_GENES, MIR608, MIR4651, MIR4534, MIR3192_5P, MIR8082, MANNO_MIDBRAIN_NEUROTYPES_HSERT, HARALAMBIEVA_PBMC_M_M_R_II_AGE_11_22YO_VACCINATED_VS_UNVACCINATED_7YR_DN, HE_LIM_SUN_FETAL_LUNG_C1_SMG_CELL, GSE24142_ADULT_VS_FETAL_DN2_THYMOCYTE_UP, WP_1P36_COPY_NUMBER_VARIATION_SYNDROME, PULVER_FOREY_CELLCYCLE_PEAKING_EG1

GO Biological Process (0):

GO Molecular Function (0):

GO Cellular Component (1): membrane (GO:0016020)

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
cellular anatomical structure1

Protein interactions and networks

STRING

416 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
FNDC10FNDC7Q5VTL7616
FNDC10FANK1Q8TC84456
FNDC10LRFN5Q96NI6428
FNDC10CRTAC1Q9NQ79419
FNDC10FLRT1Q9NZU1404
FNDC10IGFN1Q86VF2401
FNDC10FLRT2O43155333
FNDC10FNDC9Q8TBE3324
FNDC10FNDC1Q4ZHG4321
FNDC10TARM1B6A8C7317
FNDC10ANKFN1Q8N957279
FNDC10SLPIP03973254
FNDC10CFAP97Q9P2B7247
FNDC10FNDC5Q8NAU1245
FNDC10SFRP5Q5T4F7243

IntAct

2 interactions, top by confidence:

ABTypeScore
SLC22A1FNDC10psi-mi:“MI:0914”(association)0.350

BioGRID (3): C1orf233 (Affinity Capture-MS), C1orf233 (Affinity Capture-RNA), C1orf233 (Affinity Capture-MS)

ESM2 similar proteins: A2A9Q0, A5PKD8, A9JSM3, D4A2Q0, E7ERA6, F1SAM7, F2Z333, P0CG25, Q07303, Q0IIA6, Q1RMK9, Q24JP5, Q2MJR0, Q2WF71, Q3MIP1, Q3UV16, Q3ZCQ3, Q504Y2, Q5EBM0, Q5GH56, Q5GH64, Q5GH72, Q5RJI4, Q5SZI1, Q641Q3, Q6IEE6, Q6IQX7, Q6P6N5, Q6UKI2, Q6ZMC9, Q6ZVW7, Q86UD0, Q8IUW3, Q8IZ52, Q8K064, Q8N4K4, Q8NAC3, Q8NBR0, Q8NCL9, Q8NFR9

Diamond homologs: A2A9Q0, D4A2Q0, F2Z333

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic1
Likely pathogenic0
Uncertain significance0
Likely benign1
Benign0

Top pathogenic / likely-pathogenic (1)

Variant IDHGVSClassification
523269GRCh37/hg19 1p36.33-36.31(chr1:834101-6076140)Pathogenic

SpliceAI

98 predictions. Top by Δscore:

VariantEffectΔscore
1:1598396:GGCT:Gacceptor_gain0.7600
1:1598395:AGGCT:Aacceptor_gain0.7300
1:1598397:GCT:Gacceptor_gain0.7200
1:1598398:C:Aacceptor_gain0.7200
1:1598399:T:Aacceptor_gain0.6900
1:1599418:C:CTdonor_gain0.6700
1:1599419:C:CTdonor_gain0.6300
1:1598394:AAGGC:Aacceptor_gain0.4800
1:1598406:G:GAacceptor_gain0.4700
1:1599449:CGCCG:Cdonor_gain0.4700
1:1599471:T:TAdonor_gain0.4600
1:1599417:A:ACdonor_gain0.4200
1:1599160:C:CAdonor_gain0.4000
1:1599335:T:TAdonor_gain0.3900
1:1599287:AGGCG:Adonor_gain0.3800
1:1598380:CCC:Cacceptor_gain0.3700
1:1598381:CCC:Cacceptor_gain0.3700
1:1598389:A:Cacceptor_gain0.3600
1:1598641:AC:Adonor_gain0.3500
1:1598642:CC:Cdonor_gain0.3500
1:1599274:G:Tdonor_gain0.3500
1:1599400:C:CTdonor_gain0.3500
1:1599401:C:CTdonor_gain0.3500
1:1599445:C:Tdonor_gain0.3500
1:1599446:C:Tdonor_gain0.3500
1:1599450:G:Tdonor_gain0.3500
1:1599891:A:ACdonor_gain0.3500
1:1599292:C:CAdonor_gain0.3400
1:1599233:T:TGacceptor_gain0.3200
1:1598714:CCCT:Cdonor_loss0.3100

AlphaMissense

1415 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
1:1599412:A:GC202R0.999
1:1599426:A:TM197K0.999
1:1599498:A:CF173C0.999
1:1599660:A:CF119C0.999
1:1599680:C:AW112C0.999
1:1599680:C:GW112C0.999
1:1599737:C:AW93C0.999
1:1599737:C:GW93C0.999
1:1599852:A:CF55C0.999
1:1599426:A:CM197R0.998
1:1599498:A:GF173S0.998
1:1599627:C:TC130Y0.998
1:1599411:C:TC202Y0.997
1:1599432:C:TC195Y0.997
1:1599433:A:GC195R0.997
1:1599435:A:TI194N0.997
1:1599497:G:CF173L0.997
1:1599497:G:TF173L0.997
1:1599499:A:GF173L0.997
1:1599621:T:AD132V0.997
1:1599699:A:CF106C0.997
1:1599410:G:CC202W0.996
1:1599423:A:TL198Q0.996
1:1599429:A:TV196D0.996
1:1599626:G:CC130W0.996
1:1599628:A:GC130R0.996
1:1599654:C:TC121Y0.996
1:1599408:A:GL203P0.995
1:1599444:C:TG191D0.995
1:1599455:C:AM187I0.995

dbSNP variants (sampled 300 via entrez): RS1000869921 (1:1597932 G>C), RS1000895193 (1:1600589 G>A), RS1001276122 (1:1599364 C>G,T), RS1001357756 (1:1601939 T>C), RS1001384644 (1:1598176 C>G), RS1001493233 (1:1599684 G>A,C,T), RS1001881160 (1:1598399 T>A,C), RS1003032696 (1:1601143 G>A), RS1003148933 (1:1601325 T>C,G), RS1003368451 (1:1599332 G>C), RS1003483385 (1:1600393 C>A,T), RS1003902994 (1:1598689 C>T), RS1003956773 (1:1598468 G>A), RS1005056310 (1:1601337 C>T), RS1005380251 (1:1600617 C>A,T)

Disease associations

OMIM: gene `` | disease phenotypes:

GenCC curated gene-disease

Mondo (1): dilated cardiomyopathy (MONDO:0005021)

Orphanet (1): Dilated cardiomyopathy (Orphanet:217604)

HPO phenotypes

1 total (1 of 1 shown, HPO-id order):

HPOTerm
HP:0001644Dilated cardiomyopathy

GWAS associations

1 associations (top):

StudyTraitp-value
GCST005951_34Body mass index3.000000e-08

EFO canonical traits (1, from GWAS)

EFO IDTrait name
EFO:0004340body mass index

MeSH disease descriptors (1)

DescriptorNameTree numbers
D002311Cardiomyopathy, DilatedC14.280.195.160; C14.280.238.070; C16.320.488.750

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

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

CTD chemical–gene interactions

22 total (human), top 22 by PubMed support.

ChemicalActions (top 5)PubMed papers
sodium arsenitedecreases expression2
Tobacco Smoke Pollutiondecreases expression2
bisphenol Aaffects expression1
2-methyl-4-isothiazolin-3-onedecreases expression1
ethyl-p-hydroxybenzoatedecreases expression1
ferrous chloridedecreases expression1
di-n-butylphosphoric acidaffects expression1
abrinedecreases expression1
jinfukangaffects cotreatment, increases expression1
Air Pollutantsdecreases expression, increases abundance1
Cisplatinaffects cotreatment, increases expression1
Doxorubicindecreases expression1
Leadaffects expression1
Methotrexatedecreases expression1
Niclosamideincreases expression1
Smokedecreases expression1
Thimerosaldecreases expression1
Thiramdecreases expression1
Valproic Acidaffects expression1
1-Methyl-4-phenylpyridiniumincreases expression1
Acrylamidedecreases expression1
Particulate Matterdecreases expression, increases abundance1

Clinical trials (associated diseases)

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

TrialPhaseStatusTitle
NCT00374465PHASE4UNKNOWNTherapy With Verapamil or Carvedilol in Chronic Heart Failure
NCT01293903PHASE4COMPLETEDStudy of Qiliqiangxin Capsule to Treat Dilated Cardiomyopathy
NCT01557140PHASE4COMPLETEDA Randomized Trial of Carvedilol in Chronic Chagas Cardiomyopathy
NCT01917149PHASE4COMPLETEDSupramaximal Titrated Inhibition of RAAS in Dilated Cardiomyopathy
NCT02115581PHASE4COMPLETEDCoenzyme Q10 Supplementation in Children With Idiopathic Dilated Cardiomyopathy
NCT06236022PHASE4RECRUITINGThe Effects of Sirolimus in Patients With Dilated Cardiomyopathy Infected With Kaposi Sarcoma-associated Virus
NCT00333827PHASE3COMPLETEDCell Therapy In Dilated Cardiomyopathy
NCT00505154PHASE3COMPLETEDEffect of Rosuvastatin on Left Ventricular Remodeling
NCT01223703PHASE3COMPLETEDPUFAs and Left Ventricular Function in Heart Failure
NCT01583114PHASE3TERMINATEDPREclinical Mutation CARriers From Families With DIlated Cardiomyopathy and ACE Inhibitors
NCT01914081PHASE3UNKNOWNResveratrol: A Potential Anti- Remodeling Agent in Heart Failure, From Bench to Bedside
NCT02989181PHASE3UNKNOWNContinues Positive Airway Pressure Treatment for Patients With Dilated Cardiomyopathy and Obstructive Sleep Apnea
NCT03439514PHASE3TERMINATEDA Study of ARRY-371797 (PF-07265803) in Patients With Symptomatic Dilated Cardiomyopathy Due to a Lamin A/C Gene Mutation
NCT05237323PHASE3COMPLETEDMicophenolate Mofetil Versus Azathioprine in Myocarditis
NCT05849766PHASE3COMPLETEDEffect of Dapagliflozin on Cardiac Structure, Function and Secondary Mitral Regurgitation in Patients with Left Ventricle Dysfunction
NCT06250257PHASE3RECRUITINGBromocriptine in Dilated Cardiomyopathy Among Women of Reproductive Age
NCT00629018PHASE2COMPLETEDSafety and Efficacy Study of Stem Cell Transplantation to Treat Dilated Cardiomyopathy
NCT00629096PHASE2COMPLETEDIntracoronary Infusion of Autologous Bone Marrow Cells for Treatment of Idiopathic Dilated Cardiomyopathy
NCT00765518PHASE2COMPLETEDUse of Ixmyelocel-T (Formerly Cardiac Repair Cell [CRC] Treatment) in Patients With Heart Failure Due to Dilated Cardiomyopathy (IMPACT-DCM)
NCT00847964PHASE2COMPLETEDSafety and Feasibility of Algisyl-LVR™ as a Method of Left Ventricular Restoration in Patients With DCM Undergoing Open-heart Surgery
NCT01020968PHASE2COMPLETEDUse of Ixmyelocel-T (Formerly Catheter-based Cardiac Repair Cell [CRC]) Treatment in Patients With Heart Failure Due to Dilated Cardiomyopathy
NCT01302171PHASE2COMPLETEDBone Marrow Derived Adult Stem Cells for Dilated Cardiomyopathy
NCT01350310PHASE2COMPLETEDSafety and Efficacy Study of Intramyocardial Stem Cell Therapy in Patients With Dilated Cardiomyopathy
NCT02133911PHASE2COMPLETEDA Pilot Trial of Ranolazine to Treat Patients With Dilated Cardiomyopathy
NCT03071653PHASE2SUSPENDEDLeft Cardiac Sympathetic Denervation for Cardiomyopathy Feasibility Pilot Study
NCT03572660PHASE2ACTIVE_NOT_RECRUITINGUse of Bone Marrow Derived Stem Cell and G-CSF With Circulatory Assistance in the Treatment of DCM
NCT03775070PHASE2COMPLETEDSimvastatin Therapy in Patients With Dilated Cardiomyopathy.
NCT04405804PHASE2UNKNOWNEarly Administration of Ivabradine in Children With Heart Failure
NCT05410873PHASE2COMPLETEDExamining the Effects of Mitochondrial Oxidative Stress in DCM
NCT06632834PHASE2RECRUITINGOutcome-targeted Therapy: Principle and Outcome Evaluation: Clinical Study and Phenotype-genotype Correlation
NCT00585546PHASE1TERMINATEDHarefield Recovery Protocol Study for Patients With Refractory Chronic Heart Failure
NCT02293603PHASE1UNKNOWNDilated cardiomYopathy iNtervention With Allogeneic MyocardIally-regenerative Cells (DYNAMIC)
NCT03062956PHASE1COMPLETEDA Single Ascending Dose Study Assessing the Safety, Tolerability, PK and PD of MYK-491
NCT03129568PHASE1COMPLETEDTranscoronary Infusion of Cardiac Progenitor Cells in Pediatric Dilated Cardiomyopathy
NCT04982081PHASE1UNKNOWNTreating Congestive HF With hiPSC-CMs Through Endocardial Injection
NCT06381466PHASE1TERMINATEDA Study to Investigate Safety, Tolerability, and Pharmacokinetics of Oral AZD0233 Compared With Placebo in Healthy Adult Participants.
NCT06464588PHASE1RECRUITINGA Phase 1 Open-Label Study of the Safety of Intravenous Allogeneic Neonatal Mesenchymal Cells (nMSCs) in Young Adult (1A) and Pediatric (1B) Patients With Dilated Cardiomyopathy (DCM)
NCT06902896PHASE1COMPLETEDSafety and Efficacy of FAP iCDC in End-stage Dilated Cardiomyopathy
NCT07137338PHASE1RECRUITINGA Phase 1 AAV Gene Therapy Trial Evaluating Safety and Preliminary Efficacy of RP-A701 in Subjects With BAG3 Dilated Cardiomyopathy
NCT07241104PHASE1RECRUITINGA Study of AZD4063 in PLN R14del Dilated Cardiomyopathy

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