SMIM33

gene
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Summary

SMIM33 (small integral membrane protein 33, HGNC:53645) is a protein-coding gene on chromosome 5q31.2, encoding Small integral membrane protein 33 (A0A1B0GW64).

Predicted to be located in membrane.

Source: NCBI Gene 111064649 — RefSeq curated summary.

At a glance

  • MANE Select transcript: NM_001365197

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:53645
Approved symbolSMIM33
Namesmall integral membrane protein 33
Location5q31.2
Locus typegene with protein product
StatusApproved
Ensembl geneENSG00000283288
Ensembl biotypeprotein_coding
Entrez111064649

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 protein_coding

ENST00000637503

RefSeq mRNA: 1 — MANE Select: NM_001365197 NM_001365197

CCDS: CCDS93790

Canonical transcript exons

ENST00000637503 — 2 exons

ExonStartEnd
ENSE00003798128139472532139473700
ENSE00003799688139471004139471130

Expression profiles

Bgee: expression breadth broad, 22 present calls, max score 67.96.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
mucosa of transverse colonUBERON:000499167.96gold quality
rectumUBERON:000105263.08gold quality
bone marrow cellCL:000209256.13gold quality
duodenumUBERON:000211454.92gold quality
granulocyteCL:000009452.18gold quality
transverse colonUBERON:000115751.86gold quality
colonic epitheliumUBERON:000039750.28gold quality
vermiform appendixUBERON:000115447.38gold quality
olfactory segment of nasal mucosaUBERON:000538646.03silver quality
small intestineUBERON:000210845.56gold quality
gall bladderUBERON:000211044.95gold quality
small intestine Peyer’s patchUBERON:000345444.74gold quality
minor salivary glandUBERON:000183044.19gold quality
intestineUBERON:000016043.89gold quality
saliva-secreting glandUBERON:000104443.67gold quality
colonUBERON:000115543.08gold quality
lymph nodeUBERON:000002941.91gold quality
sural nerveUBERON:001548841.15gold quality
stromal cell of endometriumCL:000225539.51gold quality
ganglionic eminenceUBERON:000402338.87gold quality
muscle tissueUBERON:000238538.58silver quality
apex of heartUBERON:000209836.91gold quality
smooth muscle tissueUBERON:000113536.54gold quality
skeletal muscle tissueUBERON:000113436.51gold quality
ventricular zoneUBERON:000305336.48gold quality
cortical plateUBERON:000534336.47gold quality
hindlimb stylopod muscleUBERON:000425236.42gold quality
primary visual cortexUBERON:000243636.09gold quality
monocyteCL:000057635.16gold quality
fallopian tubeUBERON:000388935.00silver quality

Single-cell (SCXA)

Detected in 1 experiment(s), a significant marker in 0.

ExperimentMarker?Max mean expression
E-ANND-3no2.08

Regulation

Is transcription factor: no

Cross-species orthologs

2 orthologs

OrganismSymbolGene ID
mus_musculusSmim33ENSMUSG00000073598
rattus_norvegicusENSRNOG00000079652

Protein

Protein identifiers

Small integral membrane protein 33A0A1B0GW64 (reviewed: A0A1B0GW64)

All UniProt accessions (1): A0A1B0GW64

UniProt curated annotations — full annotation on UniProt →

Subcellular location. Membrane.

RefSeq proteins (1): NP_001352126* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR038803SMIM33Family

UniProt features (5 total): region of interest 2, chain 1, transmembrane region 1, glycosylation site 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-A0A1B0GW64-F162.220.11

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 (1): 15

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 2 (showing top): DARWICHE_PAPILLOMA_PROGRESSION_RISK, chr5q31

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

102 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
SMIM33SPATA24Q86W54665
SMIM33DNAJC18Q9H819623
SMIM33PROB1E7EW31571
SMIM33FAM13BQ9NYF5499
SMIM33LRRTM2O43300496
SMIM33SIL1Q9H173476
SMIM33PKD2L2Q9NZM6476
SMIM33FAM221BA6H8Z2417
SMIM33ECSCRQ19T08403
SMIM33NME5P56597400
SMIM33BRD8Q9H0E9368
SMIM33SLC23A1Q9UHI7368
SMIM33ATP10AO60312359
SMIM33STING1Q86WV6353
SMIM33CDC23Q9UJX2349

IntAct

0 interactions, top by confidence:

ESM2 similar proteins: A0A1B0GW64, A0A5F4BST2, A0PJX4, A8MVS5, A8MWV9, B0FP48, E5RIL1, E9PGG2, O14836, O60320, O95998, P09564, Q01113, Q01114, Q13477, Q2KI80, Q2T9R2, Q3TS39, Q3UPR0, Q3URD2, Q4V9L6, Q5FVJ4, Q5M869, Q6A044, Q6UWJ8, Q75VT8, Q864V4, Q8BRJ3, Q8BX43, Q8C503, Q8IVY1, Q8K5A9, Q8N112, Q8NC24, Q8NDY8, Q8QZT4, Q8R138, Q969Z4, Q9BUF7, Q9CQM1

Diamond homologs: A0A1B0GW64, Q3TS39

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance0
Likely benign0
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

139 predictions. Top by Δscore:

VariantEffectΔscore
5:139472610:C:Gdonor_gain0.9400
5:139472604:G:GTdonor_gain0.9100
5:139472606:GGTGC:Gdonor_gain0.8900
5:139472654:G:GAdonor_gain0.8900
5:139472609:GC:Gdonor_gain0.8600
5:139472658:ACC:Adonor_gain0.8600
5:139472705:GGC:Gdonor_gain0.8100
5:139472657:C:Adonor_gain0.7800
5:139472653:T:TAdonor_gain0.7600
5:139472784:G:GAdonor_gain0.7600
5:139472594:G:GTdonor_gain0.7400
5:139472616:G:GAdonor_gain0.7400
5:139472638:T:Gdonor_gain0.7300
5:139472783:T:TAdonor_gain0.7300
5:139472688:G:GTdonor_gain0.7200
5:139472583:G:GTdonor_gain0.6800
5:139472690:A:AGacceptor_gain0.6700
5:139472691:G:GGacceptor_gain0.6700
5:139472595:C:Tdonor_gain0.6500
5:139472625:G:Tdonor_gain0.6500
5:139472706:G:GTdonor_gain0.6500
5:139472686:T:Aacceptor_gain0.6300
5:139472625:G:GTdonor_gain0.6100
5:139472668:T:TAdonor_gain0.6100
5:139472904:G:GTdonor_gain0.5900
5:139472615:T:TAdonor_gain0.5800
5:139472919:T:TAdonor_gain0.5700
5:139472920:A:AAdonor_gain0.5700
5:139472607:GTGC:Gdonor_gain0.5200
5:139472608:TGCT:Tdonor_gain0.5200

AlphaMissense

838 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
5:139472676:T:CF52L0.963
5:139472678:T:AF52L0.963
5:139472678:T:GF52L0.963
5:139472694:T:CC58R0.963
5:139472689:C:AA56E0.941
5:139472680:T:AV53D0.930
5:139472804:G:CW94C0.923
5:139472804:G:TW94C0.923
5:139472701:T:AI60K0.912
5:139472683:T:GL54R0.889
5:139472692:T:AV57D0.889
5:139472802:T:AW94R0.874
5:139472802:T:CW94R0.874
5:139472686:T:GL55R0.854
5:139472668:T:AV49D0.853
5:139472701:T:GI60R0.849
5:139472677:T:GF52C0.842
5:139472710:T:AV63D0.837
5:139472698:T:AI59N0.829
5:139472677:T:CF52S0.823
5:139472665:T:AI48N0.811
5:139472671:C:AA50D0.789
5:139472803:G:TW94L0.786
5:139472698:T:CI59T0.782
5:139472683:T:AL54Q0.771
5:139472698:T:GI59S0.771
5:139472688:G:CA56P0.765
5:139472676:T:AF52I0.759
5:139472674:T:AV51D0.758
5:139472715:T:CF65L0.757

dbSNP variants (sampled 300 via entrez): RS1000577520 (5:139469884 A>AT), RS1000884653 (5:139469658 G>T), RS1001316995 (5:139469452 G>A), RS1001819796 (5:139469117 G>A), RS1002853592 (5:139473908 C>T), RS1002923375 (5:139472024 C>T), RS1003227575 (5:139473669 C>T), RS1004458866 (5:139473406 G>A), RS1004581428 (5:139473131 C>CG), RS1005103487 (5:139472864 C>T), RS1005480927 (5:139473273 C>T), RS1005784409 (5:139470701 G>A,T), RS1006074219 (5:139471938 G>T), RS1006484319 (5:139470664 C>T), RS1006518095 (5:139471770 G>A)

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)

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.