SMIM10

gene
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Summary

SMIM10 (small integral membrane protein 10, HGNC:41913) is a protein-coding gene on chromosome Xq26.3, encoding Small integral membrane protein 10 (Q96HG1).

Predicted to be located in membrane.

Source: NCBI Gene 644538 — RefSeq curated summary.

At a glance

  • Clinical variants (ClinVar): 10 total
  • MANE Select transcript: NM_001163438

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:41913
Approved symbolSMIM10
Namesmall integral membrane protein 10
LocationXq26.3
Locus typegene with protein product
StatusApproved
Ensembl geneENSG00000184785
Ensembl biotypeprotein_coding
Entrez644538

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 protein_coding

ENST00000330288

RefSeq mRNA: 1 — MANE Select: NM_001163438 NM_001163438

CCDS: CCDS55502

Canonical transcript exons

ENST00000330288 — 1 exons

ExonStartEnd
ENSE00001324955134990991134992473

Expression profiles

Bgee: expression breadth ubiquitous, 176 present calls, max score 94.20.

FANTOM5 (CAGE): breadth ubiquitous, TPM avg 7.4502 / max 99.4042, expressed in 1271 samples.

FANTOM5 promoters (3 alternative TSS)

Promoter IDTPM avgSamples expressed
1976197.14191268
1976170.175393
1976180.133157

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
popliteal arteryUBERON:000225094.20gold quality
tibial arteryUBERON:000761094.19gold quality
right coronary arteryUBERON:000162594.13gold quality
calcaneal tendonUBERON:000370192.98gold quality
left coronary arteryUBERON:000162692.89gold quality
aortaUBERON:000094792.64gold quality
coronary arteryUBERON:000162191.73gold quality
thoracic aortaUBERON:000151590.99gold quality
ascending aortaUBERON:000149690.90gold quality
descending thoracic aortaUBERON:000234590.79gold quality
C1 segment of cervical spinal cordUBERON:000646990.55gold quality
right testisUBERON:000453489.16gold quality
left testisUBERON:000453388.20gold quality
buccal mucosa cellCL:000233688.07silver quality
spinal cordUBERON:000224087.76gold quality
tibial nerveUBERON:000132387.21gold quality
lower esophagus muscularis layerUBERON:003583386.77gold quality
lower esophagusUBERON:001347386.71gold quality
testisUBERON:000047386.52gold quality
esophagogastric junction muscularis propriaUBERON:003584186.36gold quality
left uterine tubeUBERON:000130386.10gold quality
left adrenal gland cortexUBERON:003582585.90gold quality
left adrenal glandUBERON:000123485.75gold quality
endocervixUBERON:000045885.26gold quality
right adrenal glandUBERON:000123385.14gold quality
mucosa of stomachUBERON:000119984.67gold quality
muscle layer of sigmoid colonUBERON:003580584.67gold quality
right adrenal gland cortexUBERON:003582784.41gold quality
body of uterusUBERON:000985384.25gold quality
adrenal cortexUBERON:000123584.16gold quality

Single-cell (SCXA)

Detected in 2 experiment(s), a significant marker in 2.

ExperimentMarker?Max mean expression
E-HCAD-6yes52.82
E-ANND-3yes5.58

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

53 targeting SMIM10, 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-3064-3P100.0070.091254
HSA-MIR-548C-3P99.9974.017587
HSA-MIR-3692-3P99.9870.272139
HSA-MIR-4715-3P99.9866.03670
HSA-MIR-60799.9773.625593
HSA-MIR-551B-5P99.9671.283493
HSA-MIR-1250-3P99.9670.044038
HSA-MIR-548Y99.9471.283514
HSA-MIR-335-3P99.9373.364958
HSA-MIR-367199.9073.043897
HSA-MIR-153-5P99.8973.866317
HSA-MIR-5582-3P99.8672.484221
HSA-MIR-576-5P99.8470.462582
HSA-MIR-808099.8267.521342
HSA-MIR-6756-5P99.8267.972466
HSA-MIR-3150A-3P99.7664.441640
HSA-MIR-6763-5P99.7664.681767
HSA-MIR-7856-5P99.7569.992901
HSA-MIR-494-3P99.7071.452795
HSA-MIR-130399.6569.771662
HSA-MIR-317599.6566.302031
HSA-MIR-4743-3P99.6268.122095
HSA-MIR-6758-3P99.5767.551078
HSA-MIR-432899.5771.064094
HSA-MIR-57899.4668.361787
HSA-MIR-4652-3P99.3370.022742
HSA-MIR-2115-3P99.3169.682026
HSA-MIR-397899.2468.392201
HSA-MIR-4477B99.2370.491733
HSA-MIR-6734-3P99.1566.271627

Literature-anchored findings (GeneRIF, showing 1)

  • Therefore, these data suggest that SMIM10 exerts an oncosuppressive role in melanoma cells.Taken together, our results unveil the potential of S. cerevisiae to study hBRAFV600E, to populate the network of its functional interactors and, in doing so, to uncover new cancer-associated genes with therapeutic potential (PMID:30237439)

Cross-species orthologs

1 orthologs

OrganismSymbolGene ID
danio_reriosmim10l3ENSDARG00000100331

Paralogs (4): SMIM10L2A (ENSG00000178947), SMIM10L2B (ENSG00000196972), SMIM10L1 (ENSG00000256537), SMIM10L3 (ENSG00000286075)

Protein

Protein identifiers

Small integral membrane protein 10Q96HG1 (reviewed: Q96HG1)

All UniProt accessions (1): Q96HG1

UniProt curated annotations — full annotation on UniProt →

Subcellular location. Membrane.

RefSeq proteins (1): NP_001156910* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR029367SMIM10Family

Pfam: PF15118

UniProt features (2 total): chain 1, transmembrane region 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q96HG1-F167.050.00

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 35 (showing top): GSE45365_CD8A_DC_VS_CD11B_DC_IFNAR_KO_MCMV_INFECTION_UP, chrXq26, RYBP_TARGET_GENES, ZNF2_TARGET_GENES, ZNF592_TARGET_GENES, ZNF618_TARGET_GENES, ZNF660_TARGET_GENES, ZSCAN30_TARGET_GENES, MIR7856_5P, MIR3978, MIR4743_3P, MIR4297, MIR3977, MIR4330, GSE12366_NAIVE_VS_MEMORY_BCELL_UP

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

6 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
SMIM10BRAFP15056257
SMIM10MUC15Q8N3870
SMIM10TOMM6Q96B490

IntAct

0 interactions, top by confidence:

ESM2 similar proteins: A0A023PXF2, A0A0C4DGP1, A0LE50, A6X974, C0QIZ2, I2HB70, O30141, O60756, P05678, P0C5L6, P0DQF8, P0DXX6, P11304, P17142, P34249, P36153, P38470, P38726, P39550, P39566, P40326, P40365, P40521, P40551, P40575, P40895, P47020, P53056, P54949, P59471, P87264, P92534, P93284, P93302, Q02918, Q03913, Q04909, Q12506, Q3E7Z1, Q5QFB9

Diamond homologs: A0A0C4DGP1, P0DMW3, P0DMW4, P0DMW5, Q5U425, Q96HG1

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance10
Likely benign0
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

85 predictions. Top by Δscore:

VariantEffectΔscore
X:134991490:A:AGacceptor_gain0.5400
X:134991491:G:GGacceptor_gain0.5400
X:134991331:TGCAG:Tdonor_loss0.5000
X:134991333:CAG:Cdonor_loss0.5000
X:134991334:AG:Adonor_loss0.5000
X:134991335:GG:Gdonor_loss0.5000
X:134991336:G:GAdonor_loss0.5000
X:134991337:T:Gdonor_loss0.5000
X:134991316:T:Gdonor_gain0.4500
X:134991995:C:Gacceptor_gain0.4500
X:134991028:G:GTdonor_gain0.4200
X:134991333:C:Tdonor_gain0.3900
X:134991073:GGTCG:Gdonor_gain0.3700
X:134991074:GTCGG:Gdonor_gain0.3700
X:134991075:TCGGT:Tdonor_gain0.3700
X:134991315:A:AGdonor_gain0.3600
X:134991925:A:Cacceptor_gain0.3500
X:134991074:GTCG:Gdonor_gain0.3300
X:134991492:T:Gacceptor_gain0.3300
X:134991994:A:AGacceptor_gain0.3300
X:134992032:A:AGacceptor_gain0.3300
X:134992033:G:GGacceptor_gain0.3300
X:134991491:GTAT:Gacceptor_gain0.3200
X:134991338:A:Gdonor_loss0.3000
X:134991491:GTATA:Gacceptor_gain0.2900
X:134991083:TC:Tdonor_gain0.2800
X:134991899:TGG:Tacceptor_gain0.2800
X:134991921:CCCAA:Cacceptor_gain0.2800
X:134991491:GT:Gacceptor_gain0.2700
X:134991076:C:CAdonor_gain0.2600

AlphaMissense

518 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
X:134991219:T:CF42L0.924
X:134991221:C:AF42L0.924
X:134991221:C:GF42L0.924
X:134991255:T:CF54L0.886
X:134991257:C:AF54L0.886
X:134991257:C:GF54L0.886
X:134991285:T:CF64L0.817
X:134991287:C:AF64L0.817
X:134991287:C:GF64L0.817
X:134991265:C:AA57D0.719
X:134991252:T:CF53L0.712
X:134991254:C:AF53L0.712
X:134991254:C:GF53L0.712
X:134991227:G:CK44N0.706
X:134991227:G:TK44N0.706
X:134991269:G:CW58C0.685
X:134991269:G:TW58C0.685
X:134991267:T:AW58R0.670
X:134991267:T:CW58R0.670
X:134991232:T:AL46H0.661
X:134991255:T:AF54I0.659
X:134991307:C:AA71D0.647
X:134991220:T:GF42C0.644
X:134991220:T:CF42S0.636
X:134991276:C:AR61S0.617
X:134991235:C:AT47K0.607
X:134991256:T:GF54C0.599
X:134991313:T:AV73E0.586

dbSNP variants (sampled 300 via entrez): RS1000713221 (X:134991831 T>C), RS1002215013 (X:134990821 C>T), RS1002568923 (X:134990169 A>G), RS1002928843 (X:134992039 G>A), RS1004186601 (X:134990030 T>C), RS1004217889 (X:134989361 T>G), RS1004238998 (X:134990747 T>A), RS1004551165 (X:134992636 T>G), RS1005678328 (X:134989592 C>T), RS1005921312 (X:134989039 G>C,T), RS1011768781 (X:134992566 G>A), RS1011911147 (X:134989428 C>T), RS1012950181 (X:134992026 T>C), RS1013331536 (X:134991317 T>C), RS1013481295 (X:134991724 A>AG)

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

0 associations (top):

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

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

CTD chemical–gene interactions

11 total (human), top 11 by PubMed support.

ChemicalActions (top 5)PubMed papers
bisphenol Adecreases methylation1
S-(1,2-dichlorovinyl)cysteineaffects response to substance, increases expression1
Sunitinibdecreases expression1
Benzo(a)pyreneaffects methylation1
Diethylstilbestroldecreases expression1
Estradiolaffects cotreatment, decreases expression1
Lipopolysaccharidesdecreases expression, affects response to substance, increases expression1
Nickeldecreases expression1
Tobacco Smoke Pollutiondecreases expression1
Tretinoindecreases expression1
Aflatoxin B1decreases 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.