SLC48A1
Heme transporter HRG1
Also known as: FLJ20489, hHRG-1, HRG1, HRG1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q6P1K1
- Gene
- SLC48A1
- Ensembl
- ENSG00000211584
- Chromosome
- 12
- Canonical length
- 146 aa
- Protein class
- Predicted intracellular proteins, Predicted membrane proteins, Transporters
- Subcellular location
- Vesicles
OverviewNCBI Gene
Enables heme binding activity and heme transmembrane transporter activity. Involved in heme transport. Located in endosome membrane; lysosomal membrane; and plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
146 residues, UniProt reviewed canonical sequence.
>Q6P1K1|SLC48A1
1 MAPSRLQLGL RAAYSGISSV AGFSIFLVWT VVYRQPGTAA MGGLAGVLAL WVLVTHVMYM
61 QDYWRTWLKG LRGFFFVGVL FSAVSIAAFC TFLVLAITRH QSLTDPTSYY LSSVWSFISF
121 KWAFLLSLYA HRYRADFADI SILSDFLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SLC48A1 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
- 4
- Mean surface accessibility (rSASA)
- 0.31
- Highest tissue expression
- 131 nTPM
Expression across tissuesHPA
Tissue
- spinal cord: 131 nTPM
- basal ganglia: 95 nTPM
- midbrain: 94 nTPM
- hippocampal formation: 91 nTPM
- amygdala: 77 nTPM
- cerebral cortex: 72 nTPM
Single-cell type
- oligodendrocytes: 142 nCPM
- esophageal apical cells: 105 nCPM
- podocytes: 82 nCPM
- renal collecting duct principal cells: 58 nCPM
- astrocytes: 54 nCPM
- epicardial cells: 52 nCPM
Immune cell
- neutrophil: 37 nTPM
- classical monocyte: 18 nTPM
- intermediate monocyte: 14 nTPM
- myeloid DC: 13 nTPM
- eosinophil: 12 nTPM
- memory B-cell: 10 nTPM
Brain region
- white matter: 190 nTPM
- basal ganglia: 188 nTPM
- midbrain: 180 nTPM
- medulla oblongata: 179 nTPM
- thalamus: 178 nTPM
- cerebellum: 159 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)
- 0.68
- gnomAD pLI
- 0.73
- gnomAD missense Z
- 0.77
- DepMap mean gene effect
- -0.09
- 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
- erythrocyte differentiation
- heme export
- heme metabolic process
- heme transport
- localization of cell
- lysosomal transport
- phagocytosis
- heme export from vacuole to cytoplasm
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Heme transporter HRG
- Haem-transporter, endosomal/lysosomal, haem-responsive gene
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads SLC48A1 as an antibody target. Whether an autoantibody or antibody against SLC48A1 could matter depends on whether native SLC48A1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SLC48A1 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 SLC48A1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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