MARCHF10

gene
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Also known as FLJ35757MARCH-X

Summary

MARCHF10 (membrane associated ring-CH-type finger 10, HGNC:26655) is a protein-coding gene on chromosome 17q23.2, encoding Probable E3 ubiquitin-protein ligase MARCHF10 (Q8NA82). E3 ubiquitin-protein ligase.

MARCH10 is a member of the MARCH family of membrane-bound E3 ubiquitin ligases (EC 6.3.2.19). MARCH enzymes add ubiquitin (see MIM 191339) to target lysines in substrate proteins, thereby signaling their vesicular transport between membrane compartments (Morokuma et al., 2007 [PubMed 17604280]).

Source: NCBI Gene 162333 — RefSeq curated summary.

At a glance

  • Clinical variants (ClinVar): 135 total
  • MANE Select transcript: NM_152598

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:26655
Approved symbolMARCHF10
Namemembrane associated ring-CH-type finger 10
Location17q23.2
Locus typegene with protein product
StatusApproved
AliasesFLJ35757, MARCH-X
Ensembl geneENSG00000173838
Ensembl biotypeprotein_coding
OMIM613337
Entrez162333

Gene structure

Transcript identifiers

Ensembl transcripts: 14 — 11 protein_coding, 3 protein_coding_CDS_not_defined

ENST00000311269, ENST00000456609, ENST00000544856, ENST00000578346, ENST00000579620, ENST00000580520, ENST00000582358, ENST00000582568, ENST00000583600, ENST00000583803, ENST00000858437, ENST00000858438, ENST00000948244, ENST00000948245

RefSeq mRNA: 4 — MANE Select: NM_152598 NM_001100875, NM_001288779, NM_001288780, NM_152598

CCDS: CCDS11635, CCDS74122, CCDS74123

Canonical transcript exons

ENST00000311269 — 11 exons

ExonStartEnd
ENSE000011810226272248862722597
ENSE000011810266272493862725104
ENSE000011810316273593162737332
ENSE000012351286270553962705581
ENSE000012351336271123162711344
ENSE000012351596274437662744528
ENSE000012351686275983562760006
ENSE000027038946280807762808314
ENSE000035569936278848062788599
ENSE000035649186270131462701758
ENSE000035941226280164662801752

Expression profiles

Bgee: expression breadth ubiquitous, 153 present calls, max score 98.05.

FANTOM5 (CAGE): breadth tissue_specific, TPM avg 0.5136 / max 242.6837, expressed in 143 samples.

FANTOM5 promoters (6 alternative TSS)

Promoter IDTPM avgSamples expressed
1674390.214132
1674350.128562
1674380.104036
1674400.03865
1674370.01754
1674410.01106

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
left testisUBERON:000453398.05gold quality
right testisUBERON:000453498.03gold quality
right uterine tubeUBERON:000130296.82gold quality
testisUBERON:000047394.46gold quality
olfactory segment of nasal mucosaUBERON:000538688.64gold quality
spermCL:000001985.77gold quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099184.76gold quality
adenohypophysisUBERON:000219684.32gold quality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047384.23gold quality
pituitary glandUBERON:000000783.37gold quality
bronchial epithelial cellCL:000232879.52gold quality
buccal mucosa cellCL:000233679.01gold quality
bronchusUBERON:000218577.99gold quality
fallopian tubeUBERON:000388973.82gold quality
nerveUBERON:000102172.99gold quality
tibial nerveUBERON:000132372.99gold quality
nasal cavity mucosaUBERON:000182672.69gold quality
oviduct epitheliumUBERON:000480471.80gold quality
adult organismUBERON:000702371.72gold quality
right lungUBERON:000216771.66gold quality
nasal cavity epitheliumUBERON:000538470.29gold quality
caudate nucleusUBERON:000187370.12gold quality
myocardiumUBERON:000234969.93gold quality
nucleus accumbensUBERON:000188268.04gold quality
putamenUBERON:000187467.91gold quality
left uterine tubeUBERON:000130367.33gold quality
pancreatic ductal cellCL:000207966.86silver quality
metanephros cortexUBERON:001053366.81gold quality
islet of LangerhansUBERON:000000666.40gold quality
left ventricle myocardiumUBERON:000656666.39gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3yes8.59

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

22 targeting MARCHF10, 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-223-3P99.9970.141140
HSA-MIR-30A-3P99.8769.742928
HSA-MIR-30D-3P99.8769.922917
HSA-MIR-30E-3P99.8769.682942
HSA-MIR-449299.8768.253611
HSA-MIR-132199.8465.301811
HSA-MIR-473999.8465.251832
HSA-MIR-4756-5P99.8464.981809
HSA-MIR-378G99.7164.901106
HSA-MIR-29B-2-5P99.6768.981726
HSA-MIR-545-5P99.6670.182308
HSA-MIR-613299.6065.831554
HSA-MIR-6836-5P99.6065.621538
HSA-MIR-432899.5771.064094
HSA-MIR-1207-5P99.4969.112983
HSA-MIR-3191-3P99.4563.94356
HSA-MIR-942-3P98.8169.04876
HSA-MIR-513B-3P98.7668.121577
HSA-MIR-58398.7167.441791
HSA-MIR-446398.5666.051071
HSA-MIR-6810-5P98.2966.21975
HSA-MIR-6880-5P98.0865.591282

Cross-species orthologs

2 orthologs

OrganismSymbolGene ID
mus_musculusMarchf10ENSMUSG00000078627
rattus_norvegicusMarchf10ENSRNOG00000007084

Paralogs (1): MARCHF7 (ENSG00000136536)

Protein

Protein identifiers

Probable E3 ubiquitin-protein ligase MARCHF10Q8NA82 (reviewed: Q8NA82)

Alternative names: Membrane-associated RING finger protein 10, Membrane-associated RING-CH protein X, RING finger protein 190, RING-type E3 ubiquitin transferase MARCHF10

All UniProt accessions (7): Q8NA82, A0A140VKA1, G3V1Q5, J3KTK3, J3KTN9, J3QLJ2, J3QRH7

UniProt curated annotations — full annotation on UniProt →

Function. E3 ubiquitin-protein ligase. E3 ubiquitin ligases accept ubiquitin from an E2 ubiquitin-conjugating enzyme in the form of a thioester and then directly transfer the ubiquitin to targeted substrates.

Domain organisation. The RING-CH-type zinc finger domain is required for E3 ligase activity.

Pathway. Protein modification; protein ubiquitination.

RefSeq proteins (4): NP_001094345, NP_001275708, NP_001275709, NP_689811* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR011016Znf_RING-CHDomain
IPR013083Znf_RING/FYVE/PHDHomologous_superfamily
IPR042583MARCH10_RING_CH-C4HC3Domain
IPR052297RING-CH-type_E3_ubiq-ligaseFamily

Pfam: PF12906

UniProt features (23 total): binding site 8, region of interest 4, compositionally biased region 4, sequence variant 3, sequence conflict 2, chain 1, zinc finger region 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q8NA82-F150.330.08

Functional residue map

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

Ligand- & substrate-binding residues (8): 659; 662; 677; 679; 687; 690; 711; 714

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 68 (showing top): TCF4_Q5, TGACATY_UNKNOWN, GOBP_POST_TRANSLATIONAL_PROTEIN_MODIFICATION, PPARA_01, NIKOLSKY_BREAST_CANCER_17Q21_Q25_AMPLICON, IVANOVA_HEMATOPOIESIS_STEM_CELL_LONG_TERM, STAT5A_01, GOMF_ACYLTRANSFERASE_ACTIVITY, GOMF_AMINOACYLTRANSFERASE_ACTIVITY, GOMF_UBIQUITIN_LIKE_PROTEIN_LIGASE_ACTIVITY, HSF2_01, DODD_NASOPHARYNGEAL_CARCINOMA_DN, MEISSNER_NPC_HCP_WITH_H3K4ME2, MIKKELSEN_IPS_HCP_WITH_H3_UNMETHYLATED, HSF1_01

GO Biological Process (1): protein ubiquitination (GO:0016567)

GO Molecular Function (5): zinc ion binding (GO:0008270), ubiquitin protein ligase activity (GO:0061630), protein binding (GO:0005515), transferase activity (GO:0016740), metal ion binding (GO:0046872)

GO Cellular Component (0):

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
protein modification by small protein conjugation1
transition metal ion binding1
ubiquitin-protein transferase activity1
ubiquitin-like protein ligase activity1
binding1
catalytic activity1
cation binding1

Protein interactions and networks

STRING

634 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
MARCHF10MARCHF11A6NNE9742
MARCHF10MARCHF9Q86YJ5643
MARCHF10MARCHF3Q86UD3627
MARCHF10MARCHF4Q9P2E8582
MARCHF10EFCAB3Q8N7B9570
MARCHF10TSSK4Q6SA08514
MARCHF10QRICH1Q2TAL8510
MARCHF10CFAP100Q494V2471
MARCHF10TEKT4Q8WW24466
MARCHF10ROPN1Q9HAT0464
MARCHF10CFAP44Q96MT7462
MARCHF10CABYRO75952462
MARCHF10METTL2AQ96IZ6453
MARCHF10ODF2Q5BJF6452
MARCHF10SPATA6Q9NWH7447

IntAct

34 interactions, top by confidence:

ABTypeScore
UNC45AMARCHF10psi-mi:“MI:0915”(physical association)0.780
MARCHF10UNC45Apsi-mi:“MI:0915”(physical association)0.780
MARCHF10NTAQ1psi-mi:“MI:0915”(physical association)0.560
MARCHF10ANLNpsi-mi:“MI:0915”(physical association)0.560
NTAQ1MARCHF10psi-mi:“MI:0915”(physical association)0.560
ANLNMARCHF10psi-mi:“MI:0915”(physical association)0.560
GCD7MARCHF10psi-mi:“MI:0915”(physical association)0.560
MARCHF10GCD7psi-mi:“MI:0915”(physical association)0.560
MARCHF10psi-mi:“MI:0915”(physical association)0.560
MARCHF10HTRA2psi-mi:“MI:0915”(physical association)0.560
MARCHF10JPH3psi-mi:“MI:0915”(physical association)0.560
MARCHF10SPRED1psi-mi:“MI:0915”(physical association)0.560
SRPK2MARCHF10psi-mi:“MI:0217”(phosphorylation reaction)0.440
MARCHF10Dlg4psi-mi:“MI:0407”(direct interaction)0.440
CTBP1MARCHF10psi-mi:“MI:0915”(physical association)0.370

BioGRID (10): MARCH10 (Two-hybrid), MARCH10 (Two-hybrid), MARCH10 (Two-hybrid), MARCH10 (Two-hybrid), MARCH10 (Two-hybrid), MARCH10 (Affinity Capture-MS), MARCH10 (Two-hybrid), APP (Reconstituted Complex), MARCH10 (Biochemical Activity), MARCH10 (Two-hybrid)

ESM2 similar proteins: A0A1B0GTS1, A0A1B0GWH4, A1A4L6, A1YGI6, A6NDR6, B8QB46, F1MJR8, F1QDF8, O35892, O35893, P09015, P15036, P15037, P23497, P52729, P59598, Q32NH9, Q3KRF1, Q3UM89, Q4G112, Q4V7E1, Q5M7N6, Q5ND04, Q5XIV2, Q5ZHX5, Q66IG8, Q6P1R3, Q6PCX9, Q6PJQ5, Q708W2, Q76I76, Q76I79, Q76N89, Q7M6U3, Q8AXQ4, Q8BVK9, Q8IUE0, Q8IUE1, Q8IWB6, Q8IXJ9

Diamond homologs: A0JN69, F4JKK0, P32225, P40318, P90489, Q0IH10, Q0P496, Q0VD59, Q1LVZ2, Q28EX7, Q28IK8, Q32L65, Q3TZ87, Q5I0I2, Q5PQ35, Q5R9W2, Q5T0T0, Q5XH39, Q5XI50, Q5XIE5, Q5XIV2, Q68FA7, Q6NZQ8, Q80TE3, Q86UD3, Q86YJ5, Q8BRX9, Q8NA82, Q8TCQ1, Q93227, Q99M02, Q9DBD2, Q9DHV7, Q9H992, Q9P0N8, Q9P2E8, Q9WV66, A6NNE9, A6P320, O60103

SIGNOR signaling

1 interactions.

AEffectBMechanism
Ub:E2“up-regulates activity”MARCHF10ubiquitination

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance89
Likely benign19
Benign17

Top pathogenic / likely-pathogenic (0)

SpliceAI

2615 predictions. Top by Δscore:

VariantEffectΔscore
17:62711225:ACTT:Adonor_loss1.0000
17:62711226:CTTA:Cdonor_loss1.0000
17:62711227:TTACC:Tdonor_loss1.0000
17:62711228:TACC:Tdonor_loss1.0000
17:62711229:A:Cdonor_loss1.0000
17:62711229:AC:Adonor_gain1.0000
17:62711230:CC:Cdonor_gain1.0000
17:62711230:CCCT:Cdonor_gain1.0000
17:62788595:CAAGC:Cacceptor_gain1.0000
17:62801641:ATTAC:Adonor_loss1.0000
17:62801642:TTAC:Tdonor_loss1.0000
17:62801643:TA:Tdonor_loss1.0000
17:62801644:AC:Adonor_loss1.0000
17:62801645:CCTGA:Cdonor_loss1.0000
17:62711224:GACTT:Gdonor_loss0.9900
17:62711229:A:ACdonor_gain0.9900
17:62711230:C:CCdonor_gain0.9900
17:62711240:TTCC:Tdonor_gain0.9900
17:62711341:GTGCC:Gacceptor_loss0.9900
17:62711342:TGCC:Tacceptor_loss0.9900
17:62711343:GCC:Gacceptor_loss0.9900
17:62711345:C:Aacceptor_loss0.9900
17:62711345:C:CCacceptor_gain0.9900
17:62722482:TCTTA:Tdonor_loss0.9900
17:62722483:CTTAC:Cdonor_loss0.9900
17:62722484:TTACC:Tdonor_loss0.9900
17:62722485:TACC:Tdonor_loss0.9900
17:62722486:ACCT:Adonor_loss0.9900
17:62722487:CC:Cdonor_loss0.9900
17:62722599:T:Cacceptor_gain0.9900

AlphaMissense

5344 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
17:62724960:C:AW694C0.996
17:62724960:C:GW694C0.996
17:62724962:A:GW694R0.995
17:62724962:A:TW694R0.995
17:62724974:A:GC690R0.994
17:62724985:A:TV686D0.994
17:62722561:C:GC714S0.993
17:62722562:A:TC714S0.993
17:62724958:A:GL695P0.992
17:62724972:G:CC690W0.991
17:62724973:C:GC690S0.991
17:62724974:A:TC690S0.991
17:62725067:A:GC659R0.991
17:62725060:A:GI661T0.990
17:62725066:C:GC659S0.990
17:62725067:A:TC659S0.990
17:62722562:A:GC714R0.989
17:62725007:A:GC679R0.989
17:62724996:G:CS682R0.988
17:62724996:G:TS682R0.988
17:62724998:T:GS682R0.988
17:62724970:A:GL691P0.987
17:62725057:C:GC662S0.986
17:62725058:A:GC662R0.986
17:62725058:A:TC662S0.986
17:62725065:A:CC659W0.985
17:62722560:A:CC714W0.984
17:62722570:C:TC711Y0.984
17:62722571:A:GC711R0.984
17:62724981:A:CH687Q0.984

dbSNP variants (sampled 300 via entrez): RS1000026204 (17:62787256 A>C), RS1000085879 (17:62701049 T>C), RS1000088082 (17:62740769 G>C), RS1000091224 (17:62799645 C>T), RS1000152299 (17:62701234 T>C), RS1000159338 (17:62787032 A>C), RS1000182228 (17:62701508 G>T), RS1000226476 (17:62768881 T>C), RS1000251984 (17:62737620 T>C), RS1000335183 (17:62757060 A>C), RS1000336203 (17:62725842 C>T), RS1000364693 (17:62739941 G>T), RS1000373874 (17:62779917 C>A), RS1000397620 (17:62773135 G>A), RS1000424940 (17:62707002 G>A)

Disease associations

OMIM: gene MIM:613337 | disease phenotypes: MIM:618906

GenCC curated gene-disease

Mondo (1): intellectual developmental disorder with autistic features and language delay, with or without seizures (MONDO:0030051)

Orphanet (0):

HPO phenotypes

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

GWAS associations

0 associations (top):

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

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

CTD chemical–gene interactions

12 total (human), top 12 by PubMed support.

ChemicalActions (top 5)PubMed papers
ethyl-p-hydroxybenzoatedecreases expression1
sodium arseniteincreases expression1
benzo(e)pyreneincreases methylation1
abrineincreases expression1
Resveratrolaffects cotreatment, decreases expression1
Air Pollutantsincreases abundance, increases expression1
Benzo(a)pyreneaffects methylation, decreases methylation, increases methylation1
Copperaffects cotreatment, decreases expression1
Methapyrileneincreases methylation1
Smokeincreases expression1
Tobacco Smoke Pollutiondecreases expression1
Particulate Matterincreases abundance, increases expression1

Clinical trials (associated diseases)

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