TMEM241
UDP-N-acetylglucosamine transporter TMEM241
Also known as: C18orf45, FLJ44259, MGC11386, TM241_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q24JQ0
- Gene
- TMEM241
- Ensembl
- ENSG00000134490
- Chromosome
- 18
- Canonical length
- 296 aa
- Protein class
- Predicted membrane proteins, Transporters
- Subcellular location
- Golgi apparatus,Vesicles
OverviewNCBI Gene
Enables UDP-N-acetylglucosamine transmembrane transporter activity. Involved in UDP-N-acetylglucosamine transmembrane transport. Located in Golgi apparatus. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
296 residues, UniProt reviewed canonical sequence.
>Q24JQ0|TMEM241
1 MCVRRSLVGL TFCTCYLASY LTNKYVLSVL KFTYPTLFQG WQTLIGGLLL HVSWKLGWVE
61 INSSSRSHVL VWLPASVLFV GIIYAGSRAL SRLAIPVFLT LHNVAEVIIC GYQKCFQKEK
121 TSPAKICSAL LLLAAAGCLP FNDSQFNPDG YFWAIIHLLC VGAYKILQKS QKPSALSDID
181 QQYLNYIFSV VLLAFASHPT GDLFSVLDFP FLYFYRFHGS CCASGFLGFF LMFSTVKLKN
241 LLAPGQCAAW IFFAKIITAG LSILLFDAIL TSATTGCLLL GALGEALLVF SERKSSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against TMEM241 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
- 9
- Mean surface accessibility (rSASA)
- 0.26
- Highest tissue expression
- 2.7 nTPM
Expression across tissuesHPA
Tissue
- smooth muscle: 2.7 nTPM
- cerebral cortex: 2.5 nTPM
- parathyroid gland: 2.3 nTPM
- breast: 2.1 nTPM
- placenta: 2.1 nTPM
- rectum: 2.1 nTPM
Single-cell type
- endometrial glandular cells: 389 nCPM
- adipocytes: 190 nCPM
- podocytes: 174 nCPM
- fibro-adipogenic progenitors: 145 nCPM
- melanocytes: 142 nCPM
- salivary acinar cells: 130 nCPM
Immune cell
- NK-cell: 6 nTPM
- intermediate monocyte: 2.2 nTPM
- naive B-cell: 2.2 nTPM
- myeloid DC: 2 nTPM
- MAIT T-cell: 1.3 nTPM
- memory B-cell: 1.3 nTPM
Brain region
- cerebral cortex: 6.4 nTPM
- white matter: 5.1 nTPM
- basal ganglia: 4.3 nTPM
- choroid plexus: 4 nTPM
- hippocampal formation: 3.8 nTPM
- hypothalamus: 3.1 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)
- 0.95
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.24
- DepMap mean gene effect
- 0.1
- DepMap dependency class
- none
OntologyGO
Biological processes
- UDP-N-acetylglucosamine transmembrane transport
- GDP-mannose transmembrane transport
Molecular functions
- antiporter activity
- UDP-N-acetylglucosamine transmembrane transporter activity
- GDP-mannose transmembrane transporter activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads TMEM241 as an antibody target. Whether an autoantibody or antibody against TMEM241 could matter depends on whether native TMEM241 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TMEM241 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 TMEM241 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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