SLC39A9
Zinc transporter ZIP9
Also known as: FLJ11274, S39A9_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9NUM3
- Gene
- SLC39A9
- Ensembl
- ENSG00000029364
- Chromosome
- 14
- Canonical length
- 307 aa
- Protein class
- Predicted membrane proteins, Transporters
- Subcellular location
- Endoplasmic reticulum
OverviewNCBI Gene
Enables G protein-coupled receptor activity; androgen binding activity; and zinc efflux transmembrane transporter activity. Involved in intracellular zinc ion homeostasis; regulation of vascular endothelial cell proliferation; and zinc ion transmembrane transport. Located in several cellular components, including mitochondrial membrane; perinuclear region of cytoplasm; and trans-Golgi network. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
307 residues, UniProt reviewed canonical sequence.
>Q9NUM3|SLC39A9
1 MDDFISISLL SLAMLVGCYV AGIIPLAVNF SEERLKLVTV LGAGLLCGTA LAVIVPEGVH
61 ALYEDILEGK HHQASETHNV IASDKAAEKS VVHEHEHSHD HTQLHAYIGV SLVLGFVFML
121 LVDQIGNSHV HSTDDPEAAR SSNSKITTTL GLVVHAAADG VALGAAASTS QTSVQLIVFV
181 AIMLHKAPAA FGLVSFLMHA GLERNRIRKH LLVFALAAPV MSMVTYLGLS KSSKEALSEV
241 NATGVAMLFS AGTFLYVATV HVLPEVGGIG HSHKPDATGG RGLSRLEVAA LVLGCLIPLI
301 LSVGHQHLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SLC39A9 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
- Cell surface
- Secreted
- No
- Transmembrane segments
- 8
- Mean surface accessibility (rSASA)
- 0.32
- Highest tissue expression
- 41 nTPM
Expression across tissuesHPA
Tissue
- liver: 41 nTPM
- salivary gland: 32 nTPM
- kidney: 28 nTPM
- pancreas: 27 nTPM
- parathyroid gland: 25 nTPM
- epididymis: 24 nTPM
Single-cell type
- hepatocytes: 91 nCPM
- somatotrophs: 91 nCPM
- salivary acinar cells: 88 nCPM
- choroid plexus epithelial cells: 84 nCPM
- lactotrophs: 83 nCPM
- parietal cells: 81 nCPM
Immune cell
- myeloid DC: 11 nTPM
- basophil: 11 nTPM
- classical monocyte: 10 nTPM
- intermediate monocyte: 9.7 nTPM
- eosinophil: 9.4 nTPM
- non-classical monocyte: 9.4 nTPM
Brain region
- choroid plexus: 33 nTPM
- white matter: 30 nTPM
- hypothalamus: 28 nTPM
- spinal cord: 28 nTPM
- thalamus: 28 nTPM
- cerebellum: 26 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)
- 0.48
- gnomAD pLI
- 0.73
- gnomAD missense Z
- 1.97
- DepMap mean gene effect
- -0.08
- 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
Biological processes
- bicellular tight junction assembly
- intracellular zinc ion homeostasis
- regulation of vascular endothelial cell proliferation
- zinc ion transmembrane transport
- regulation of cellular response to testosterone stimulus
Molecular functions
- androgen binding
- G protein-coupled receptor activity
- zinc efflux transmembrane transporter activity
- zinc ion transmembrane transporter activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Zinc/iron permease
- ZIP Zinc transporter
- Zinc transporter ZIP9
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads SLC39A9 as an antibody target. Whether an autoantibody or antibody against SLC39A9 could matter depends on whether native SLC39A9 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SLC39A9 is annotated at the cell surface, where native SLC39A9 is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label SLC39A9 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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