CNNM3
Metal transporter CNNM3
Also known as: ACDP3, CNNM3_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8NE01
- Gene
- CNNM3
- Ensembl
- ENSG00000168763
- Chromosome
- 2
- Canonical length
- 707 aa
- Protein class
- Predicted membrane proteins, Transporters
- Subcellular location
- Cytosol
OverviewNCBI Gene
Predicted to enable transmembrane transporter activity. Predicted to be involved in magnesium ion homeostasis. Located in membrane. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
707 residues, UniProt reviewed canonical sequence.
>Q8NE01|CNNM3
1 MAAAVAAAGR LGWLFAALCL GNAAGEAAPG PRVLGFCLEE DGAAGAGWVR GGAARDTPDA
61 TFLLRLFGPG FANSSWSWVA PEGAGCREEA ASPAGEWRAL LRLRLRAEAV RPHSALLAVR
121 VEPGGGAAEE AAPPWALGLG AAGLLALAAL ARGLQLSALA LAPAEVQVLR ESGSEAERAA
181 ARRLEPARRW AGCALGALLL LASLAQAALA VLLYRAAGQR AVPAVLGSAG LVFLVGEVVP
241 AAVSGRWTLA LAPRALGLSR LAVLLTLPVA LPVGQLLELA ARPGRLRERV LELARGGGDP
301 YSDLSKGVLR CRTVEDVLTP LEDCFMLDAS TVLDFGVLAS IMQSGHTRIP VYEEERSNIV
361 DMLYLKDLAF VDPEDCTPLS TITRFYNHPL HFVFNDTKLD AVLEEFKRGK SHLAIVQKVN
421 NEGEGDPFYE VLGLVTLEDV IEEIIRSEIL DESEDYRDTV VKRKPASLMA PLKRKEEFSL
481 FKVSDDEYKV TISPQLLLAT QRFLSREVDV FSPLRISEKV LLHLLKHPSV NQEVRFDESN
541 RLATHHYLYQ RSQPVDYFIL ILQGRVEVEI GKEGLKFENG AFTYYGVSAL TVPSSVHQSP
601 VSSLQPIRHD LQPDPGDGTH SSAYCPDYTV RALSDLQLIK VTRLQYLNAL LATRAQNLPQ
661 SPENTDLQVI PGSQTRLLGE KTTTAAGSSH SRPGVPVEGS PGRNPGVLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CNNM3 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
- 4
- Mean surface accessibility (rSASA)
- 0.42
- Highest tissue expression
- 42 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 42 nTPM
- pancreas: 25 nTPM
- liver: 20 nTPM
- parathyroid gland: 20 nTPM
- cerebellum: 20 nTPM
- duodenum: 16 nTPM
Single-cell type
- hepatocytes: 49 nCPM
- epicardial cells: 46 nCPM
- cardiomyocytes: 45 nCPM
- retinal horizontal cells: 42 nCPM
- gastric chief cells: 36 nCPM
- parietal cells: 35 nCPM
Immune cell
- eosinophil: 3.5 nTPM
- neutrophil: 3.3 nTPM
- gdT-cell: 2.6 nTPM
- T-reg: 2.2 nTPM
- memory CD8 T-cell: 2.1 nTPM
- naive B-cell: 2.1 nTPM
Brain region
- cerebellum: 33 nTPM
- white matter: 27 nTPM
- basal ganglia: 23 nTPM
- cerebral cortex: 22 nTPM
- medulla oblongata: 21 nTPM
- midbrain: 21 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)
- 0.97
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.76
- 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
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of CNNM3 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 CNNM3 as an antibody target. Whether an autoantibody or antibody against CNNM3 could matter depends on whether native CNNM3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CNNM3 is annotated at the cell surface, where native CNNM3 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 CNNM3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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