TMEM38A
Trimeric intracellular cation channel type A
Also known as: MGC3169, TM38A_HUMAN, TRIC-A
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9H6F2
- Gene
- TMEM38A
- Ensembl
- ENSG00000072954
- Chromosome
- 19
- Canonical length
- 299 aa
- Protein class
- Predicted membrane proteins
- Subcellular location
- Nucleoplasm
- Quaternary structure
- Homotrimer
OverviewNCBI Gene
Predicted to enable potassium channel activity. Predicted to be involved in regulation of release of sequestered calcium ion into cytosol. Predicted to act upstream of or within several processes, including cellular response to caffeine; monoatomic cation transmembrane transport; and regulation of cardiac muscle contraction by regulation of the release of sequestered calcium ion. Located in extracellular exosome. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
299 residues, UniProt reviewed canonical sequence.
>Q9H6F2|TMEM38A
1 MELLSALSLG ELALSFSRVP LFPVFDLSYF IVSILYLKYE PGAVELSRRH PIASWLCAML
61 HCFGSYILAD LLLGEPLIDY FSNNSSILLA SAVWYLIFFC PLDLFYKCVC FLPVKLIFVA
121 MKEVVRVRKI AVGIHHAHHH YHHGWFVMIA TGWVKGSGVA LMSNFEQLLR GVWKPETNEI
181 LHMSFPTKAS LYGAILFTLQ QTRWLPVSKA SLIFIFTLFM VSCKVFLTAT HSHSSPFDAL
241 EGYICPVLFG SACGGDHHHD NHGGSHSGGG PGAQHSAMPA KSKEELSEGS RKKKAKKADLocalizationUniProt · AlphaFold · HPA
Whether an antibody against TMEM38A can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Other membrane
- Secreted
- No
- Transmembrane segments
- 7
- Mean surface accessibility (rSASA)
- 0.36
- Highest tissue expression
- 544 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 544 nTPM
- tongue: 242 nTPM
- choroid plexus: 101 nTPM
- cerebral cortex: 28 nTPM
- basal ganglia: 25 nTPM
- heart muscle: 25 nTPM
Single-cell type
- myonuclei: 848 nCPM
- thymic myoid cells: 193 nCPM
- cone photoreceptor cells: 174 nCPM
- retinal pigment epithelial cells: 158 nCPM
- choroid plexus epithelial cells: 102 nCPM
- epididymal clear cells: 82 nCPM
Immune cell
- basophil: 37 nTPM
- eosinophil: 12 nTPM
- naive B-cell: 6 nTPM
- memory B-cell: 4.6 nTPM
- classical monocyte: 4.2 nTPM
- NK-cell: 3.5 nTPM
Brain region
- choroid plexus: 111 nTPM
- thalamus: 34 nTPM
- hypothalamus: 33 nTPM
- cerebral cortex: 33 nTPM
- basal ganglia: 31 nTPM
- midbrain: 29 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 1.03
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.93
- DepMap mean gene effect
- -0.12
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- cellular response to caffeine
- endoplasmic reticulum organization
- regulation of cardiac muscle contraction by regulation of the release of sequestered calcium ion
- regulation of release of sequestered calcium ion into cytosol
- release of sequestered calcium ion into cytosol by sarcoplasmic reticulum
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads TMEM38A as an antibody target. Whether an autoantibody or antibody against TMEM38A could matter depends on whether native TMEM38A is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TMEM38A is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label TMEM38A as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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