MOB3C

gene
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Also known as MOB1E

Summary

MOB3C (MOB kinase activator 3C, HGNC:29800) is a protein-coding gene on chromosome 1p33, encoding MOB kinase activator 3C (Q70IA8). May regulate the activity of kinases.

The protein encoded by this gene is similar to the yeast Mob1 protein. Yeast Mob1 binds Mps1p, a protein kinase essential for spindle pole body duplication and mitotic checkpoint regulation. Alternatively spliced transcript variants encoding distinct isoforms have been observed.

Source: NCBI Gene 148932 — RefSeq curated summary.

At a glance

  • GWAS associations: 3
  • Clinical variants (ClinVar): 57 total
  • MANE Select transcript: NM_201403

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:29800
Approved symbolMOB3C
NameMOB kinase activator 3C
Location1p33
Locus typegene with protein product
StatusApproved
AliasesMOB1E
Ensembl geneENSG00000142961
Ensembl biotypeprotein_coding
OMIM620804
Entrez148932

Gene structure

Transcript identifiers

Ensembl transcripts: 8 — 8 protein_coding

ENST00000271139, ENST00000319928, ENST00000371940, ENST00000871612, ENST00000871613, ENST00000871614, ENST00000936346, ENST00000961858

RefSeq mRNA: 2 — MANE Select: NM_201403 NM_145279, NM_201403

CCDS: CCDS540

Canonical transcript exons

ENST00000319928 — 4 exons

ExonStartEnd
ENSE000018438384660771946609684
ENSE000019051264661671146616811
ENSE000035611154661290446613371
ENSE000036757144661000246610204

Expression profiles

Bgee: expression breadth ubiquitous, 242 present calls, max score 90.24.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
body of pancreasUBERON:000115090.24gold quality
granulocyteCL:000009488.69gold quality
apex of heartUBERON:000209887.85gold quality
tibialis anteriorUBERON:000138587.37silver quality
gastrocnemiusUBERON:000138887.17gold quality
muscle of legUBERON:000138386.91gold quality
right coronary arteryUBERON:000162586.81gold quality
descending thoracic aortaUBERON:000234586.57gold quality
omental fat padUBERON:001041486.37gold quality
peritoneumUBERON:000235886.34gold quality
pancreasUBERON:000126485.96gold quality
adipose tissue of abdominal regionUBERON:000780885.80gold quality
esophagogastric junction muscularis propriaUBERON:003584185.69gold quality
hindlimb stylopod muscleUBERON:000425285.65gold quality
pancreatic ductal cellCL:000207985.56silver quality
leukocyteCL:000073885.43gold quality
thoracic aortaUBERON:000151585.41gold quality
monocyteCL:000057685.34gold quality
ascending aortaUBERON:000149685.26gold quality
lower esophagusUBERON:001347384.99gold quality
lower esophagus muscularis layerUBERON:003583384.99gold quality
bloodUBERON:000017884.79gold quality
coronary arteryUBERON:000162184.77gold quality
left coronary arteryUBERON:000162684.76gold quality
right atrium auricular regionUBERON:000663184.72gold quality
vena cavaUBERON:000408784.63gold quality
lower esophagus mucosaUBERON:003583484.57gold quality
cardiac atriumUBERON:000208184.21gold quality
esophagusUBERON:000104383.97gold quality
ileal mucosaUBERON:000033183.89gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3yes4.13

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

89 targeting MOB3C, 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-8485100.0077.574731
HSA-MIR-4533100.0069.482758
HSA-MIR-4481100.0066.421669
HSA-MIR-4455100.0065.481587
HSA-MIR-196A-1-3P99.9972.152772
HSA-MIR-4745-5P99.9865.951028
HSA-MIR-807599.9767.20962
HSA-MIR-426799.9666.532368
HSA-MIR-7107-3P99.9366.73627
HSA-MIR-6753-3P99.9366.57637
HSA-MIR-515-5P99.9269.822343
HSA-MIR-519E-5P99.9269.622358
HSA-MIR-329-3P99.9166.561234
HSA-MIR-362-3P99.9166.381267
HSA-MIR-137-3P99.8774.742401
HSA-MIR-394199.8670.542735
HSA-MIR-3934-3P99.7665.511351
HSA-MIR-2681-5P99.7567.641655
HSA-MIR-4524A-3P99.7266.852406
HSA-MIR-10393-3P99.7266.56961
HSA-MIR-6801-5P99.7266.50981
HSA-MIR-320299.6667.702737
HSA-MIR-452799.6667.43714
HSA-MIR-3679-3P99.6469.881599
HSA-MIR-182799.6368.573265
HSA-MIR-24-3P99.5969.971934
HSA-MIR-211399.5871.221521
HSA-MIR-3942-3P99.5769.032854
HSA-MIR-642A-5P99.5165.101152
HSA-MIR-312899.5067.851258

Cross-species orthologs

5 orthologs

OrganismSymbolGene ID
danio_reriomob3cENSDARG00000043705
mus_musculusMob3cENSMUSG00000028709
rattus_norvegicusMob3cENSRNOG00000037620
drosophila_melanogasterMob3FBGN0259482
caenorhabditis_elegansWBGENE00020447

Paralogs (6): MOB1A (ENSG00000114978), MOB4 (ENSG00000115540), MOB3B (ENSG00000120162), MOB3A (ENSG00000172081), MOB1B (ENSG00000173542), MOB2 (ENSG00000182208)

Protein

Protein identifiers

MOB kinase activator 3CQ70IA8 (reviewed: Q70IA8)

Alternative names: Mob1 homolog 2C, Mps one binder kinase activator-like 2C

All UniProt accessions (2): Q70IA8, X6R3L3

UniProt curated annotations — full annotation on UniProt →

Function. May regulate the activity of kinases.

Similarity. Belongs to the MOB1/phocein family.

RefSeq proteins (2): NP_660322, NP_958805* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR005301MOB_kinase_act_famFamily
IPR036703MOB_kinase_act_sfHomologous_superfamily

Pfam: PF03637

UniProt features (5 total): binding site 4, chain 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q70IA8-F189.180.72

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 (4): 82; 87; 164; 169

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 103 (showing top): GSE45365_CD8A_DC_VS_CD11B_DC_IFNAR_KO_MCMV_INFECTION_UP, CREL_01, ZHAN_MULTIPLE_MYELOMA_PR_DN, LINDGREN_BLADDER_CANCER_CLUSTER_3_DN, CAGCTG_AP4_Q5, NFKB_Q6, GOMF_KINASE_ACTIVATOR_ACTIVITY, NFKB_C, TGCTGAY_UNKNOWN, PU1_Q6, LASTOWSKA_NEUROBLASTOMA_COPY_NUMBER_DN, RGAGGAARY_PU1_Q6, ACEVEDO_METHYLATED_IN_LIVER_CANCER_DN, KRIGE_RESPONSE_TO_TOSEDOSTAT_24HR_UP, GOMF_ENZYME_ACTIVATOR_ACTIVITY

GO Biological Process (1): signal transduction (GO:0007165)

GO Molecular Function (3): protein kinase activator activity (GO:0030295), metal ion binding (GO:0046872), protein binding (GO:0005515)

GO Cellular Component (2): nucleus (GO:0005634), cytoplasm (GO:0005737)

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
cell communication1
cellular process1
signaling1
regulation of cellular process1
cellular response to stimulus1
protein kinase activity1
kinase activator activity1
protein kinase regulator activity1
cation binding1
binding1
intracellular membrane-bounded organelle1
intracellular anatomical structure1
cellular anatomical structure1

Protein interactions and networks

STRING

424 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
MOB3CMOB4Q9Y3A3663
MOB3CANKDD1BA6NHY2535
MOB3CSTK38Q15208505
MOB3CMYADML2A6NDP7505
MOB3CDPH5Q9H2P9493
MOB3CNAA20P61599492
MOB3COR2T12Q8NG77474
MOB3CTMEM218A2RU14466
MOB3COR4F6Q8NGB9449
MOB3CRNGTTO60942448
MOB3CZNF117Q03924447
MOB3CCCDC144NLQ6NUI1445
MOB3COR51Q1Q8NH59438
MOB3CMARVELD1Q9BSK0423
MOB3CABHD14BQ96IU4421

IntAct

51 interactions, top by confidence:

ABTypeScore
ZBTB10MOB3Cpsi-mi:“MI:0915”(physical association)0.670
MOB3CFAM118Apsi-mi:“MI:0915”(physical association)0.670
MOB3CZBTB10psi-mi:“MI:0915”(physical association)0.670
FAM118AMOB3Cpsi-mi:“MI:0915”(physical association)0.670
MOB3CTDO2psi-mi:“MI:0915”(physical association)0.560
NT5C2MOB3Cpsi-mi:“MI:0915”(physical association)0.560
TFCP2MOB3Cpsi-mi:“MI:0915”(physical association)0.560
TNIP1MOB3Cpsi-mi:“MI:0915”(physical association)0.560
MOB3CKRT40psi-mi:“MI:0915”(physical association)0.560
SIAH1MOB3Cpsi-mi:“MI:0915”(physical association)0.560
CMTM3MOB3Cpsi-mi:“MI:0915”(physical association)0.560
TDO2MOB3Cpsi-mi:“MI:0915”(physical association)0.560
MOB3CSIAH1psi-mi:“MI:0915”(physical association)0.560
MOB3CTFCP2psi-mi:“MI:0915”(physical association)0.560
MOB3CTNIP1psi-mi:“MI:0915”(physical association)0.560
MOB3CCMTM3psi-mi:“MI:0915”(physical association)0.560
MAU2MOB3Cpsi-mi:“MI:0915”(physical association)0.560

BioGRID (383): MOB3C (Two-hybrid), MOB3C (Two-hybrid), MOB3C (Two-hybrid), MOB3C (Two-hybrid), MOB3C (Two-hybrid), MOB3C (Two-hybrid), MOB3C (Two-hybrid), MOB3C (Two-hybrid), MOB3C (Two-hybrid), MOB3C (Affinity Capture-MS), MOB3C (Affinity Capture-MS), MOB3C (Affinity Capture-RNA), MOB3C (Biochemical Activity), MOB3C (Synthetic Lethality), MOB3C (Two-hybrid)

ESM2 similar proteins: A2BG43, A8XG63, B0BNM9, B0YN54, F4K494, F4K495, O01763, O74558, O94360, P34349, P68265, P68266, Q29RK9, Q2WBN3, Q3T1J9, Q54BM4, Q54CR8, Q54QV0, Q54XJ0, Q58D63, Q5EAA4, Q5F495, Q5R5Z0, Q5RAE0, Q5RDB1, Q6NU44, Q6PEB6, Q70IA6, Q70IA8, Q7K0E3, Q7L9L4, Q86TA1, Q8BJG4, Q8BPB0, Q8BSU7, Q8GYX0, Q8VE04, Q8VI63, Q921Y0, Q949G5

Diamond homologs: F4K494, F4K495, O74558, O94360, P40484, P43563, Q29RK9, Q2LZ59, Q2WBN3, Q3T1J9, Q54BM4, Q54CR8, Q54QV0, Q54XJ0, Q58D63, Q5ABC6, Q5EAA4, Q5R5Z0, Q5RAE0, Q70IA6, Q70IA8, Q7L9L4, Q86TA1, Q8BJG4, Q8BPB0, Q8BSU7, Q8GYX0, Q8IQG1, Q8VE04, Q8VI63, Q921Y0, Q949G5, Q95RA8, Q96BX8, Q9FHI1, Q9H8S9, Q9P601, Q9VL13

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance53
Likely benign2
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

566 predictions. Top by Δscore:

VariantEffectΔscore
1:46609681:CCCT:Cacceptor_gain1.0000
1:46609682:CCTC:Cacceptor_gain1.0000
1:46609683:CT:Cacceptor_gain1.0000
1:46609685:C:CCacceptor_gain1.0000
1:46609996:CCTCA:Cdonor_loss1.0000
1:46609997:CTCAC:Cdonor_loss1.0000
1:46609998:TCA:Tdonor_loss1.0000
1:46609999:CA:Cdonor_loss1.0000
1:46610000:A:ACdonor_gain1.0000
1:46610001:C:CCdonor_gain1.0000
1:46610001:C:CTdonor_loss1.0000
1:46610202:CTC:Cacceptor_gain1.0000
1:46610203:TC:Tacceptor_gain1.0000
1:46610204:CC:Cacceptor_gain1.0000
1:46610205:C:CCacceptor_gain1.0000
1:46610206:T:Gacceptor_loss1.0000
1:46610213:C:CTacceptor_gain1.0000
1:46610214:A:Tacceptor_gain1.0000
1:46612897:CACTC:Cdonor_loss1.0000
1:46612898:ACTCA:Adonor_loss1.0000
1:46612899:CTCAC:Cdonor_loss1.0000
1:46612900:TCA:Tdonor_loss1.0000
1:46612902:A:ACdonor_gain1.0000
1:46612902:A:Cdonor_loss1.0000
1:46612903:C:CCdonor_gain1.0000
1:46612903:CCA:Cdonor_gain1.0000
1:46612903:CCAA:Cdonor_gain1.0000
1:46616611:T:Adonor_gain1.0000
1:46616709:A:ACdonor_gain1.0000
1:46616710:C:CCdonor_gain1.0000

AlphaMissense

1433 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
1:46610067:A:CY186D0.999
1:46613022:C:AW100C0.999
1:46613022:C:GW100C0.999
1:46613024:A:GW100R0.999
1:46613024:A:TW100R0.999
1:46613030:A:GY98H0.999
1:46613104:A:GL73P0.999
1:46613113:C:GR70P0.999
1:46613147:A:GW59R0.999
1:46613147:A:TW59R0.999
1:46610062:C:AK187N0.998
1:46610062:C:GK187N0.998
1:46610078:A:TV182D0.998
1:46610135:A:TV163D0.998
1:46610144:C:GR160P0.998
1:46610150:A:GL158P0.998
1:46610194:G:CF143L0.998
1:46610194:G:TF143L0.998
1:46610196:A:GF143L0.998
1:46612918:A:GF135S0.998
1:46612960:A:GL121P0.998
1:46613023:C:GW100S0.998
1:46613118:G:CF68L0.998
1:46613118:G:TF68L0.998
1:46613120:A:GF68L0.998
1:46613140:G:TA61D0.998
1:46613145:C:AW59C0.998
1:46613145:C:GW59C0.998
1:46610068:G:CC185W0.997
1:46610070:A:GC185R0.997

dbSNP variants (sampled 300 via entrez): RS1000413335 (1:46618373 C>A,G,T), RS1000721527 (1:46612502 A>G), RS1000951570 (1:46618606 G>A), RS1001470741 (1:46618264 G>A), RS1001920197 (1:46617331 C>T), RS1002724929 (1:46609179 T>C), RS1003733781 (1:46612790 C>G,T), RS1003915758 (1:46609947 C>T), RS1004097081 (1:46617203 C>G,T), RS1004302129 (1:46617358 G>A), RS1004599705 (1:46617905 A>G), RS1004749542 (1:46611713 A>T), RS1005076575 (1:46617576 C>G), RS1005466310 (1:46614776 G>A), RS1005668448 (1:46607577 C>T)

Disease associations

OMIM: gene MIM:620804 | disease phenotypes:

GenCC curated gene-disease

Mondo (0):

Orphanet (0):

HPO phenotypes

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

GWAS associations

3 associations (top):

StudyTraitp-value
GCST003050_19Schizophrenia2.000000e-06
GCST010477_5Hypertension5.000000e-07
GCST010478_4Chronic kidney disease5.000000e-08

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

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

CTD chemical–gene interactions

28 total (human), top 28 by PubMed support.

ChemicalActions (top 5)PubMed papers
Cisplatinaffects expression, affects cotreatment, increases expression2
aristolochic acid Iincreases expression1
methylmercuric chlorideincreases expression1
alpha-pineneaffects cotreatment, decreases expression, increases oxidation, increases abundance1
sodium arseniteincreases expression1
methacrylaldehydedecreases expression, increases oxidation, increases abundance, affects cotreatment1
S-(1,2-dichlorovinyl)cysteineaffects response to substance, increases expression, affects cotreatment1
di-n-butylphosphoric acidaffects expression1
erucylphospho-N,N,N-trimethylpropylammoniumincreases expression1
jinfukangaffects cotreatment, increases expression1
Decitabineaffects expression1
Sunitinibdecreases expression1
Leflunomidedecreases expression1
Acroleinaffects cotreatment, decreases expression, increases oxidation, increases abundance1
Air Pollutantsaffects cotreatment, decreases expression, increases abundance, increases oxidation1
Atrazinedecreases expression1
Benzo(a)pyrenedecreases methylation1
Doxorubicindecreases expression1
Gallic Acidincreases expression1
Lipopolysaccharidesincreases expression, affects response to substance, affects cotreatment1
Ozoneincreases oxidation, increases abundance, affects cotreatment, decreases expression1
Silicon Dioxideincreases expression1
Smokedecreases expression1
Testosteroneincreases expression1
Tobacco Smoke Pollutionincreases expression1
Valproic Acidincreases methylation1
Cadmium Chlorideincreases expression1
Volatile Organic Compoundsincreases oxidation, affects cotreatment, decreases 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.