ANO1
Anoctamin-1
Also known as: ANO1_HUMAN, DOG1, FLJ10261, ORAOV2, TAOS2, TMEM16A
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q5XXA6
- Gene
- ANO1
- Ensembl
- ENSG00000131620
- Chromosome
- 11
- Canonical length
- 986 aa
- Protein class
- Disease related genes, FDA approved drug targets, Plasma proteins, Predicted intracellular proteins, Predicted membrane proteins, Transporters
- Subcellular location
- Nucleoplasm,Plasma membrane
- Quaternary structure
- Homodimer
OverviewNCBI Gene
Enables identical protein binding activity; iodide transmembrane transporter activity; and ligand-gated monoatomic ion channel activity. Involved in several processes, including monoatomic anion transport; mucus secretion; and positive regulation of insulin secretion involved in cellular response to glucose stimulus. Located in apical plasma membrane and nucleoplasm. Implicated in Moyamoya disease. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
986 residues, UniProt reviewed canonical sequence.
>Q5XXA6|ANO1
1 MRVNEKYSTL PAEDRSVHII NICAIEDIGY LPSEGTLLNS LSVDPDAECK YGLYFRDGRR
61 KVDYILVYHH KRPSGNRTLV RRVQHSDTPS GARSVKQDHP LPGKGASLDA GSGEPPMDYH
121 EDDKRFRREE YEGNLLEAGL ELERDEDTKI HGVGFVKIHA PWNVLCREAE FLKLKMPTKK
181 MYHINETRGL LKKINSVLQK ITDPIQPKVA EHRPQTMKRL SYPFSREKQH LFDLSDKDSF
241 FDSKTRSTIV YEILKRTTCT KAKYSMGITS LLANGVYAAA YPLHDGDYNG ENVEFNDRKL
301 LYEEWARYGV FYKYQPIDLV RKYFGEKIGL YFAWLGVYTQ MLIPASIVGI IVFLYGCATM
361 DENIPSMEMC DQRHNITMCP LCDKTCSYWK MSSACATARA SHLFDNPATV FFSVFMALWA
421 ATFMEHWKRK QMRLNYRWDL TGFEEEEEAV KDHPRAEYEA RVLEKSLKKE SRNKEKRRHI
481 PEESTNKWKQ RVKTAMAGVK LTDKVKLTWR DRFPAYLTNL VSIIFMIAVT FAIVLGVIIY
541 RISMAAALAM NSSPSVRSNI RVTVTATAVI INLVVIILLD EVYGCIARWL TKIEVPKTEK
601 SFEERLIFKA FLLKFVNSYT PIFYVAFFKG RFVGRPGDYV YIFRSFRMEE CAPGGCLMEL
661 CIQLSIIMLG KQLIQNNLFE IGIPKMKKLI RYLKLKQQSP PDHEECVKRK QRYEVDYNLE
721 PFAGLTPEYM EMIIQFGFVT LFVASFPLAP LFALLNNIIE IRLDAKKFVT ELRRPVAVRA
781 KDIGIWYNIL RGIGKLAVII NAFVISFTSD FIPRLVYLYM YSKNGTMHGF VNHTLSSFNV
841 SDFQNGTAPN DPLDLGYEVQ ICRYKDYREP PWSENKYDIS KDFWAVLAAR LAFVIVFQNL
901 VMFMSDFVDW VIPDIPKDIS QQIHKEKVLM VELFMREEQD KQQLLETWME KERQKDEPPC
961 NHHNTKACPD SLGSPAPSHA YHGGVLLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ANO1 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
- 9
- Mean surface accessibility (rSASA)
- 0.33
- Highest tissue expression
- 84 nTPM
Expression across tissuesHPA
Tissue
- seminal vesicle: 84 nTPM
- epididymis: 81 nTPM
- salivary gland: 72 nTPM
- blood vessel: 69 nTPM
- liver: 43 nTPM
- skin: 41 nTPM
Single-cell type
- hepatocytes: 412 nCPM
- epididymal efferent duct absorptive cells: 363 nCPM
- breast myoepithelial cells: 244 nCPM
- epididymal principal cells: 230 nCPM
- salivary acinar cells: 215 nCPM
- late spermatids: 197 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- basal ganglia: 3.7 nTPM
- cerebral cortex: 3 nTPM
- pons: 3 nTPM
- medulla oblongata: 2.8 nTPM
- cerebellum: 2.4 nTPM
- hippocampal formation: 1.6 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about ANO1.
Disease | AllUniProt
Conditions ANO1 is implicated in, by any mechanism.
- Intestinal dysmotility syndrome (IDMTS) MIM:620045
- Moyamoya disease 7 (MYMY7) MIM:620687
Disease | GeneticClinVar
3 pathogenic / likely-pathogenic of 205 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- Moyamoya disease 7
- ANO1-related fatal neonatal disease due to impaired chloride currents
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)
- 0.33
- gnomAD pLI
- 0.87
- gnomAD missense Z
- 2.77
- DepMap mean gene effect
- -0.12
- 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
- cellular response to heat
- cellular response to peptide
- chloride transmembrane transport
- chloride transport
- detection of temperature stimulus involved in sensory perception of pain
- glial cell projection elongation
- iodide transport
- monoatomic ion transmembrane transport
- mucus secretion
- phospholipase C-activating G protein-coupled receptor signaling pathway
- protein localization to membrane
Molecular functions
- calcium-activated cation channel activity
- chloride channel activity
- identical protein binding
- intracellularly calcium-gated chloride channel activity
- iodide transmembrane transporter activity
- metal ion binding
- protein homodimerization activity
- signaling receptor binding
- voltage-gated chloride channel activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of ANO1 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 ANO1 as an antibody target. Whether an autoantibody or antibody against ANO1 could matter depends on whether native ANO1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ANO1 is annotated at the cell surface, where native ANO1 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 ANO1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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