MFSD4A
Major facilitator superfamily domain-containing protein 4A
Also known as: DKFZp761N1114, FLJ25004, FLJ34577, MFD4A_HUMAN, MFSD4, SLC60A1, UNQ3064
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8N468
- Gene
- MFSD4A
- Ensembl
- ENSG00000174514
- Chromosome
- 1
- Canonical length
- 514 aa
- Protein class
- Predicted intracellular proteins, Predicted membrane proteins, Transporters
OverviewNCBI Gene
Predicted to enable transmembrane transporter activity. Predicted to be involved in transmembrane transport. Predicted to be located in membrane. Biomarker of cholangiocarcinoma. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
514 residues, UniProt reviewed canonical sequence.
>Q8N468|MFSD4A
1 MGCDGRVSGL LRRNLQPTLT YWSVFFSFGL CIAFLGPTLL DLRCQTHSSL PQISWVFFSQ
61 QLCLLLGSAL GGVFKRTLAQ SLWALFTSSL AISLVFAVIP FCRDVKVLAS VMALAGLAMG
121 CIDTVANMQL VRMYQKDSAV FLQVLHFFVG FGALLSPLIA DPFLSEANCL PANSTANTTS
181 RGHLFHVSRV LGQHHVDAKP WSNQTFPGLT PKDGAGTRVS YAFWIMALIN LPVPMAVLML
241 LSKERLLTCC PQRRPLLLSA DELALETQPP EKEDASSLPP KFQSHLGHED LFSCCQRKNL
301 RGAPYSFFAI HITGALVLFM TDGLTGAYSA FVYSYAVEKP LSVGHKVAGY LPSLFWGFIT
361 LGRLLSIPIS SRMKPATMVF INVVGVVVTF LVLLIFSYNV VFLFVGTASL GLFLSSTFPS
421 MLAYTEDSLQ YKGCATTVLV TGAGVGEMVL QMLVGSIFQA QGSYSFLVCG VIFGCLAFTF
481 YILLLFFHRM HPGLPSVPTQ DRSIGMENSE CYQRLocalizationUniProt · AlphaFold · HPA
Whether an antibody against MFSD4A 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
- Unknown
- Secreted
- No
- Transmembrane segments
- 12
- Mean surface accessibility (rSASA)
- 0.33
- Highest tissue expression
- 125 nTPM
Expression across tissuesHPA
Tissue
- stomach: 125 nTPM
- kidney: 62 nTPM
- cerebral cortex: 32 nTPM
- cerebellum: 24 nTPM
- rectum: 17 nTPM
- salivary gland: 16 nTPM
Single-cell type
- parietal cells: 918 nCPM
- retinal bipolar cells: 239 nCPM
- loop of henle epithelial cells: 130 nCPM
- distal convoluted tubule cells: 125 nCPM
- endometrial glandular cells: 113 nCPM
- salivary duct cells: 110 nCPM
Immune cell
- naive B-cell: 0.1 nTPM
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
Brain region
- cerebral cortex: 76 nTPM
- hippocampal formation: 68 nTPM
- amygdala: 62 nTPM
- white matter: 49 nTPM
- basal ganglia: 48 nTPM
- cerebellum: 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)
- 0.7
- gnomAD pLI
- 0
- DepMap mean gene effect
- 0.02
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of MFSD4A in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads MFSD4A as an antibody target. Whether an autoantibody or antibody against MFSD4A could matter depends on whether native MFSD4A is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
MFSD4A 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 MFSD4A as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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