SMIM32
gene geneOn this page
Summary
SMIM32 (small integral membrane protein 32, HGNC:53640) is a protein-coding gene on chromosome 5q31.1, encoding Small integral membrane protein 32 (A0A1B0GUA5).
Predicted to be located in membrane.
Source: NCBI Gene 389332 — RefSeq curated summary.
At a glance
- MANE Select transcript:
NM_001350994
Identifiers
Gene identifiers
| Field | Value |
|---|---|
| HGNC ID | HGNC:53640 |
| Approved symbol | SMIM32 |
| Name | small integral membrane protein 32 |
| Location | 5q31.1 |
| Locus type | gene with protein product |
| Status | Approved |
| Ensembl gene | ENSG00000271824 |
| Ensembl biotype | protein_coding |
| Entrez | 389332 |
Gene structure
Transcript identifiers
Ensembl transcripts: 1 — 1 protein_coding
ENST00000607574
RefSeq mRNA: 1 — MANE Select: NM_001350994
NM_001350994
CCDS: CCDS87324
Canonical transcript exons
ENST00000607574 — 1 exons
| Exon | Start | End |
|---|---|---|
| ENSE00003696591 | 136191468 | 136193162 |
Expression profiles
Bgee: expression breadth broad, 92 present calls, max score 91.30.
FANTOM5 (CAGE): breadth tissue_specific, TPM avg 0.3270 / max 31.0395, expressed in 128 samples.
FANTOM5 promoters (1 alternative TSS)
| Promoter ID | TPM avg | Samples expressed |
|---|---|---|
| 63590 | 0.3270 | 128 |
Top tissues by expression
235 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| kidney epithelium | UBERON:0004819 | 91.30 | silver quality |
| adult mammalian kidney | UBERON:0000082 | 87.32 | gold quality |
| kidney | UBERON:0002113 | 81.33 | gold quality |
| duodenum | UBERON:0002114 | 81.23 | gold quality |
| mucosa of transverse colon | UBERON:0004991 | 78.78 | gold quality |
| vena cava | UBERON:0004087 | 77.51 | gold quality |
| heart right ventricle | UBERON:0002080 | 76.90 | gold quality |
| skeletal muscle tissue of biceps brachii | UBERON:0004502 | 75.42 | gold quality |
| nasal cavity epithelium | UBERON:0005384 | 73.23 | gold quality |
| renal medulla | UBERON:0000362 | 73.04 | gold quality |
| jejunal mucosa | UBERON:0000399 | 72.55 | silver quality |
| colonic mucosa | UBERON:0000317 | 72.18 | gold quality |
| adult organism | UBERON:0007023 | 71.55 | gold quality |
| metanephros cortex | UBERON:0010533 | 71.50 | gold quality |
| cortex of kidney | UBERON:0001225 | 71.40 | gold quality |
| cartilage tissue | UBERON:0002418 | 71.14 | gold quality |
| putamen | UBERON:0001874 | 71.12 | gold quality |
| jejunum | UBERON:0002115 | 70.98 | silver quality |
| metanephros | UBERON:0000081 | 70.63 | gold quality |
| mucosa of sigmoid colon | UBERON:0004993 | 70.42 | gold quality |
| myocardium | UBERON:0002349 | 70.38 | gold quality |
| lateral nuclear group of thalamus | UBERON:0002736 | 69.64 | gold quality |
| pharyngeal mucosa | UBERON:0000355 | 69.62 | gold quality |
| Brodmann (1909) area 46 | UBERON:0006483 | 69.46 | silver quality |
| upper arm skin | UBERON:0004263 | 69.41 | gold quality |
| body of tongue | UBERON:0011876 | 68.82 | gold quality |
| thymus | UBERON:0002370 | 68.81 | gold quality |
| ileal mucosa | UBERON:0000331 | 68.39 | gold quality |
| prefrontal cortex | UBERON:0000451 | 68.33 | gold quality |
| layer of synovial tissue | UBERON:0007616 | 68.18 | gold quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 1.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | yes | 5.08 |
Regulation
Is transcription factor: no
Cross-species orthologs
2 orthologs
| Organism | Symbol | Gene ID |
|---|---|---|
| mus_musculus | Smim32 | ENSMUSG00000110086 |
| rattus_norvegicus | Smim32 | ENSRNOG00000077112 |
Protein
Protein identifiers
Small integral membrane protein 32 — A0A1B0GUA5 (reviewed: A0A1B0GUA5)
All UniProt accessions (1): A0A1B0GUA5
UniProt curated annotations — full annotation on UniProt →
Subcellular location. Membrane.
RefSeq proteins (1): NP_001337923* (*=MANE)
Domains & families (InterPro)
UniProt features (2 total): chain 1, transmembrane region 1
Structure
Experimental structures (PDB)
0 structures.
Predicted structure (AlphaFold)
| Model | pLDDT | Fraction very-high |
|---|---|---|
| AF-A0A1B0GUA5-F1 | 61.35 | 0.17 |
Function
Pathways and Gene Ontology
Reactome pathways
0 pathways
MSigDB gene sets: 11 (showing top):
GSE45365_NK_CELL_VS_CD8A_DC_MCMV_INFECTION_UP, PEREZ_TP63_TARGETS, chr5q31, BLANCO_MELO_COVID19_SARS_COV_2_INFECTION_CALU3_CELLS_DN, DESCARTES_FETAL_LUNG_NEUROENDOCRINE_CELLS, DESCARTES_FETAL_PANCREAS_ISLET_ENDOCRINE_CELLS, HE_LIM_SUN_FETAL_LUNG_C1_PULMONARY_NE_PRECURSOR_CELL, HE_LIM_SUN_FETAL_LUNG_C1_PULMONARY_NEUROENDOCRINE_CELL, GSE29614_CTRL_VS_TIV_FLU_VACCINE_PBMC_2007_UP, GSE37416_CTRL_VS_0H_F_TULARENSIS_LVS_NEUTROPHIL_UP, GSE45365_HEALTHY_VS_MCMV_INFECTION_CD11B_DC_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:
| Category | Terms |
|---|---|
| cellular anatomical structure | 1 |
Protein interactions and networks
STRING
66 interactions, top by confidence (×1000):
| Protein A | Protein B | Partner UniProt | Score |
|---|---|---|---|
| SMIM32 | GNB4 | Q9HAV0 | 381 |
| SMIM32 | TMEM244 | Q5VVB8 | 380 |
| SMIM32 | GPR87 | Q9BY21 | 348 |
| SMIM32 | LYZL4 | Q96KX0 | 338 |
| SMIM32 | SACK1A | Q86UY5 | 336 |
| SMIM32 | C1orf115 | Q9H7X2 | 333 |
| SMIM32 | RASGEF1C | Q8N431 | 326 |
| SMIM32 | SLC25A21 | Q9BQT8 | 260 |
| SMIM32 | DUSP13B | Q9UII6 | 257 |
| SMIM32 | KIF16B | Q96L93 | 250 |
| SMIM32 | KLK10 | O43240 | 248 |
| SMIM32 | GNG2 | P59768 | 242 |
| SMIM32 | TFAP2D | Q7Z6R9 | 233 |
| SMIM32 | NR4A2 | P43354 | 225 |
| SMIM32 | ITGB6 | P18564 | 224 |
IntAct
0 interactions, top by confidence:
ESM2 similar proteins: A0A1B0GUA5, A0A1B0GVQ0, A0A286YF18, A0JNN8, A2VDX9, A5PK62, A6NGB7, A9CBA0, O09800, P04488, P06480, P06764, P07646, P0C171, P0DJK0, P0DJK1, P0DMQ5, P13291, P22389, P36342, P46695, P98162, Q08102, Q1RMT9, Q2HJ59, Q3TYP4, Q5BIR3, Q5EAA5, Q5JTB6, Q5NRQ0, Q6F5E0, Q6VUC0, Q6VUP9, Q703F0, Q765Z5, Q867A9, Q867D0, Q89448, Q8MJW9, Q8TEF2
SIGNOR signaling
0 interactions.
Disease & clinical
Clinical variants and AI predictions
ClinVar
0 variants total. Per-class counts are floors (≥ shown; pagination cap):
| Classification | Count (floor) |
|---|---|
| Pathogenic | 0 |
| Likely pathogenic | 0 |
| Uncertain significance | 0 |
| Likely benign | 0 |
| Benign | 0 |
Top pathogenic / likely-pathogenic (0)
SpliceAI
0 predictions. Top by Δscore:
AlphaMissense
638 scored. Top likely-pathogenic:
| Variant | Protein change | am_pathogenicity |
|---|---|---|
| 5:136192307:A:T | I73N | 0.968 |
| 5:136192340:A:C | L62R | 0.967 |
| 5:136192319:A:T | V69D | 0.958 |
| 5:136192322:A:T | L68H | 0.957 |
| 5:136192322:A:C | L68R | 0.955 |
| 5:136192340:A:T | L62Q | 0.948 |
| 5:136192309:G:C | F72L | 0.947 |
| 5:136192309:G:T | F72L | 0.947 |
| 5:136192311:A:G | F72L | 0.947 |
| 5:136192325:G:T | A67E | 0.945 |
| 5:136192279:G:C | F82L | 0.942 |
| 5:136192279:G:T | F82L | 0.942 |
| 5:136192281:A:G | F82L | 0.942 |
| 5:136192316:A:T | V70D | 0.933 |
| 5:136192343:A:C | L61R | 0.933 |
| 5:136192337:A:C | L63R | 0.931 |
| 5:136192328:A:T | V66E | 0.929 |
| 5:136192310:A:G | F72S | 0.926 |
| 5:136192340:A:G | L62P | 0.924 |
| 5:136192362:A:G | Y55H | 0.924 |
| 5:136192334:A:C | L64R | 0.921 |
| 5:136192352:A:T | L58H | 0.920 |
| 5:136192280:A:C | F82C | 0.913 |
| 5:136192334:A:T | L64H | 0.907 |
| 5:136192295:A:G | L77P | 0.904 |
| 5:136192352:A:C | L58R | 0.901 |
| 5:136192362:A:C | Y55D | 0.898 |
| 5:136192358:A:C | L56R | 0.891 |
| 5:136192378:C:A | K49N | 0.881 |
| 5:136192378:C:G | K49N | 0.881 |
dbSNP variants (sampled 300 via entrez): RS1000073020 (5:136191378 G>C), RS1000124914 (5:136191208 C>A), RS1001816935 (5:136191999 A>T), RS1001930542 (5:136192127 G>A), RS1003456973 (5:136193162 C>A,T), RS1003488235 (5:136193318 C>A,T), RS1003935642 (5:136194713 A>G), RS10045073 (5:136194216 A>G), RS1005036312 (5:136194454 G>T), RS1005135223 (5:136194409 A>C,T), RS1006082756 (5:136191663 A>C,G,T), RS1007339654 (5:136193035 C>T), RS1007826037 (5:136193187 G>T), RS1008596402 (5:136191439 GCAAA>G), RS1008837026 (5:136191731 A>G)
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
12 total (human), top 12 by PubMed support.
| Chemical | Actions (top 5) | PubMed papers |
|---|---|---|
| titanium dioxide | decreases expression | 1 |
| sodium arsenite | increases expression | 1 |
| S-(1,2-dichlorovinyl)cysteine | affects response to substance, increases expression, affects cotreatment, decreases expression | 1 |
| Air Pollutants | increases abundance, increases expression | 1 |
| Benzo(a)pyrene | increases methylation | 1 |
| Lipopolysaccharides | affects response to substance, increases expression, affects cotreatment, decreases expression | 1 |
| Malathion | decreases expression | 1 |
| Valproic Acid | decreases expression | 1 |
| Gold Compounds | decreases expression | 1 |
| Permethrin | decreases expression | 1 |
| Particulate Matter | increases abundance, increases expression | 1 |
| Magnetite Nanoparticles | decreases expression, increases methylation | 1 |
Clinical trials (associated diseases)
0 trials via MONDO — disease-level, not drug-specific.
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.