SLC30A6
Zinc transporter 6
Also known as: FLJ31101, ZNT6, ZNT6_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q6NXT4
- Gene
- SLC30A6
- Ensembl
- ENSG00000152683
- Chromosome
- 2
- Canonical length
- 461 aa
- Protein class
- Metabolic proteins, Predicted membrane proteins, Transporters
- Subcellular location
- Golgi apparatus
OverviewNCBI Gene
This gene encodes a member of a family of proteins that function as zinc transporters. This protein can regulate subcellular levels of zinc in the Golgi and vesicles. Expression of this gene is altered in the Alzheimer's disease brain plaques. [provided by RefSeq, Aug 2016]
Canonical amino-acid sequenceUniProt
461 residues, UniProt reviewed canonical sequence.
>Q6NXT4|SLC30A6
1 MGTIHLFRKP QRSFFGKLLR EFRLVAADRR SWKILLFGVI NLICTGFLLM WCSSTNSIAL
61 TAYTYLTIFD LFSLMTCLIS YWVTLRKPSP VYSFGFERLE VLAVFASTVL AQLGALFILK
121 ESAERFLEQP EIHTGRLLVG TFVALCFNLF TMLSIRNKPF AYVSEAASTS WLQEHVADLS
181 RSLCGIIPGL SSIFLPRMNP FVLIDLAGAF ALCITYMLIE INNYFAVDTA SAIAIALMTF
241 GTMYPMSVYS GKVLLQTTPP HVIGQLDKLI REVSTLDGVL EVRNEHFWTL GFGSLAGSVH
301 VRIRRDANEQ MVLAHVTNRL YTLVSTLTVQ IFKDDWIRPA LLSGPVAANV LNFSDHHVIP
361 MPLLKGTDDL NPVTSTPAKP SSPPPEFSFN TPGKNVNPVI LLNTQTRPYG FGLNHGHTPY
421 SSMLNQGLGV PGIGATQGLR TGFTNIPSRY GTNNRIGQPR PLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SLC30A6 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
- 6
- Mean surface accessibility (rSASA)
- 0.42
- Highest tissue expression
- 11 nTPM
Expression across tissuesHPA
Tissue
- placenta: 11 nTPM
- thyroid gland: 11 nTPM
- kidney: 11 nTPM
- parathyroid gland: 11 nTPM
- liver: 10 nTPM
- pancreas: 9.8 nTPM
Single-cell type
- myonuclei: 108 nCPM
- neutrophil progenitors: 67 nCPM
- somatotrophs: 66 nCPM
- syncytiotrophoblasts: 64 nCPM
- adipocytes: 63 nCPM
- lactotrophs: 61 nCPM
Immune cell
- basophil: 13 nTPM
- NK-cell: 7 nTPM
- T-reg: 4.6 nTPM
- MAIT T-cell: 3.5 nTPM
- naive CD4 T-cell: 3.4 nTPM
- naive CD8 T-cell: 3.2 nTPM
Brain region
- white matter: 16 nTPM
- cerebellum: 14 nTPM
- choroid plexus: 14 nTPM
- medulla oblongata: 14 nTPM
- spinal cord: 14 nTPM
- pons: 14 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)
- 0.87
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.03
- DepMap mean gene effect
- -0.1
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- zinc ion import into Golgi lumen
- zinc ion transport
- regulation of zinc ion transport
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Cation efflux
- Cation efflux transmembrane domain superfamily
- Cation efflux protein, transmembrane domain
- Cation efflux transmembrane domain
- Cation Diffusion Facilitator SLC30A
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of SLC30A6 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 SLC30A6 as an antibody target. Whether an autoantibody or antibody against SLC30A6 could matter depends on whether native SLC30A6 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SLC30A6 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 SLC30A6 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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