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ANO10

  • Official Full Name

    anoctamin 10

  • Overview

    The transmembrane protein encoded by this gene is a member of a family of calcium-activated chloride channels. Defects in this gene may be a cause of autosomal recessive spinocerebellar ataxia-10. Several transcript variants encoding different isoforms have been found for this gene.
  • Synonyms

    ANO10; anoctamin 10; TMEM16K, transmembrane protein 16K; anoctamin-10; FLJ10375; MGC47890; SCAR10; Hypothetical protein LOC55129; TMEM 16K; Transmembrane protein 16K; OTTHUMP00000164038; OTTHUMP00000164039; OTTHUMP00000209958; OTTHUMP00000209959; OTTHUMP00000209960; TMEM16K;
Species Cat.# Product name Source (Host) Tag Protein Length Price
Human ANO10-4838HF Recombinant Full Length Human ANO10 Protein, GST-tagged In Vitro Cell Free System GST 392 amino acids
Human ANO10-4216H Recombinant Human ANO10 Protein, GST-tagged Wheat Germ GST
Mouse ANO10-1697M Recombinant Mouse ANO10 Protein Mammalian Cell His
Mouse ANO10-567M Recombinant Mouse ANO10 Protein, His (Fc)-Avi-tagged HEK293 His (Fc)-Avi
Mouse ANO10-567M-B Recombinant Mouse ANO10 Protein Pre-coupled Magnetic Beads HEK293
  • Involved Pathway
  • Protein Function
  • Interacting Protein

ANO10 involved in several pathways and played different roles in them. We selected most pathways ANO10 participated on our site, such as Ion channel transport, Stimuli-sensing channels, Transmembrane transport of small molecules, which may be useful for your reference. Also, other proteins which involved in the same pathway with ANO10 were listed below. Creative BioMart supplied nearly all the proteins listed, you can search them on our site.

Pathway Name Pathway Related Protein
Ion channel transportTRPC4B;ASIC1A;ATP6V1G3;FXYD6-FXYD2;ATP13A5;BEST1;ATP2C1;TSC22D3;CLCN4-2
Stimuli-sensing channelsFKBP1B;TRPC5;MCOLN2;OSTM1;CLCN4-2;CLCN1A;CLCN5;ANO8;CLCNK
Transmembrane transport of small moleculesADD3B;WNK1;TTYH3B;SLC6A5;NIPAL3;SLC15A3;SLC35A1;LCN12;SLC9A9

ANO10 has several biochemical functions, for example, calcium activated cation channel activity, NOT intracellular calcium activated chloride channel activity, NOT phospholipid scramblase activity. Some of the functions are cooperated with other proteins, some of the functions could acted by ANO10 itself. We selected most functions ANO10 had, and list some proteins which have the same functions with ANO10. You can find most of the proteins on our site.

Function Related Protein
calcium activated cation channel activityCATSPER2;TRPM5;ANO6;TRPM4C;TRPM4A;ANO10;CALHM1;PKD2L1;TRPM4
NOT intracellular calcium activated chloride channel activityANO9;ANO7;ANO6;ANO5;ANO10;Ano3;ANO8
NOT phospholipid scramblase activityANO2;ANO5;ANO10

ANO10 has direct interactions with proteins and molecules. Those interactions were detected by several methods such as yeast two hybrid, co-IP, pull-down and so on. We selected proteins and molecules interacted with ANO10 here. Most of them are supplied by our site. Hope this information will be useful for your research of ANO10.

Tmem173

  • Q&As
  • Reviews

Q&As (14)

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Is ANO10 involved in any physiological processes? 03/16/2023

ANO10 may play a role in various physiological processes. For example, it has been suggested to be involved in neurotransmitter release, skeletal muscle function, and regulation of lipid metabolism. However, more research is needed to fully understand its physiological functions.

Are there any animal models for studying ANO10 dysfunction? 12/26/2022

Animal models are valuable tools for studying the function and dysfunction of genes, including ANO10. Currently, there are no specific animal models for ANO10-related disorders. However, researchers have used other animal models, such as mice and zebrafish, to study the broader functions of ANO10 or related genes. These models provide insights into the physiological roles and potential therapeutic strategies related to ANO10.

What are the current treatment options for ANO10-related disorders? 11/25/2022

Currently, there are no specific treatments available to cure or halt the progression of ANO10-related disorders. Instead, treatment focuses on managing the symptoms and improving the quality of life for affected individuals. This may involve physical therapy, occupational therapy, speech therapy, and assistive devices to cope with motor impairments and maintain independence. Additional symptom-specific medications may be prescribed to address specific symptoms such as muscle stiffness or tremors. Research is ongoing to develop targeted therapies that can address the underlying molecular mechanisms of ANO10-related disorders.

Where is ANO10 expressed in the body? 09/19/2022

ANO10 is expressed in various tissues throughout the body, including the brain, skeletal muscles, heart, liver, and kidneys.

Can ANO10 mutations be inherited? 06/21/2022

Yes, ANO10 mutations can be inherited in different patterns depending on the specific disorder. Spinocerebellar ataxia type 10 (SCA10) is primarily inherited in an autosomal dominant manner, meaning a person only needs to inherit one copy of the mutated ANO10 gene from one parent to develop the disorder. However, there are also reports of recessive inheritance patterns and de novo mutations in ANO10-related disorders. Genetic counseling and testing are essential for affected individuals and their families to determine the mode of inheritance and assess the risk of passing on the mutations to future generations.

Are there any genetic disorders associated with ANO10 mutations? 06/12/2021

Yes, mutations in the ANO10 gene have been linked to several genetic disorders. For example, mutations in ANO10 have been identified in patients with autosomal recessive spinocerebellar ataxia type 10 (SCAR10), a neurodegenerative disorder characterized by progressive cerebellar ataxia.

Can genetic testing be done to diagnose ANO10-related disorders? 01/29/2021

Yes, genetic testing can be performed to diagnose ANO10-related disorders, such as spinocerebellar ataxia type 10. Analysis of the ANO10 gene can identify pathogenic mutations that are associated with these disorders. Genetic testing is typically done through a blood or saliva sample, and it may be recommended for individuals with symptoms suggestive of ANO10-related conditions or in families with a history of these disorders.

Are there any other diseases or conditions associated with ANO10? 08/30/2020

In addition to spinocerebellar ataxia type 10, ANO10 mutations have also been reported in individuals with parkinsonism, dystonia, and craniocervical dystonia. Further research is needed to fully understand the role of ANO10 in these conditions.

Are there any potential therapeutic targets related to ANO10? 05/21/2018

Due to the limited knowledge about ANO10's exact function, potential therapeutic targets related to ANO10 are yet to be defined. However, further research into ANO10's role in cellular processes and associated diseases may provide insights for future therapeutic strategies.

Is there any ongoing research on ANO10? 09/18/2017

Yes, there is ongoing research on ANO10. Scientists are working to uncover the exact function and regulation of ANO10, as well as its roles in various diseases. This includes studying its involvement in cancer progression, exploring its potential as a therapeutic target, and investigating its role in other neurological disorders.

Can mutations in ANO10 lead to other neurological disorders? 07/22/2017

While ANO10 mutations have been primarily associated with spinocerebellar ataxia type 10, there is growing evidence linking ANO10 mutations to other neurological disorders. These include parkinsonism, dystonia, hereditary spastic paraplegia, and autosomal recessive cerebellar ataxia. Further research is necessary to fully understand the extent of ANO10's involvement in these disorders.

What are the physiological functions of ANO10? 01/13/2017

The exact physiological functions of ANO10 are not fully understood. However, studies suggest that ANO10 may play a role in a variety of cellular processes, including calcium signaling, membrane trafficking, and lipid metabolism. ANO10 has been implicated in processes such as ciliary function, autophagy, and phagocytosis. Further research is needed to fully elucidate the specific functions of ANO10 in different cell types and tissues.

Are there any other genetic disorders associated with ANO10 mutations? 12/19/2016

Yes, besides spinocerebellar ataxia type 10 (SCA10), mutations in the ANO10 gene have been associated with other disorders. For example, ANO10 mutations have been identified in individuals with autosomal recessive cerebellar ataxia and parkinsonism.

Is ANO10 associated with any cancer types? 01/06/2016

ANO10 has been implicated in the development and progression of certain cancer types. It has been found to be overexpressed in colorectal cancer, gastric cancer, and pancreatic cancer, and its upregulation is linked to poor patient prognosis. However, the exact mechanisms through which ANO10 contributes to cancer progression are still being investigated.

Customer Reviews (5)

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Reviews
09/03/2021

    The manufacturer can provide researchers with high-quality ANO10 protein, ensuring it is properly purified, characterized, and quality-controlled.

    03/16/2021

      This may include options like different formulations, protein modifications, or tagging techniques. Customization can enhance the versatility of the protein and optimize its utility in the intended research.

      08/01/2020

        They can also address any questions or concerns regarding the ANO10 protein, thereby facilitating smooth and efficient research execution.

        01/23/2019

          manufacturers may offer customization options, allowing researchers to tailor the ANO10 protein to their specific needs.

          03/05/2017

            This collaboration may extend beyond the purchase of the ANO10 protein, potentially leading to additional support, joint research projects, or access to expertise in the field.

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