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Anoctamin 5 Proteins (ANO5)

ANO5 encodes a member of the anoctamin family of transmembrane proteins. Additionally we are shipping Anoctamin 5 Antibodies (23) and Anoctamin 5 Kits (8) and many more products for this protein.

list all proteins Gene Name GeneID UniProt
ANO5 203859 Q75V66
ANO5 233246 Q75UR0
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Top Anoctamin 5 Proteins at antibodies-online.com

Showing 4 out of 5 products:

Catalog No. Origin Source Conjugate Images Quantity Supplier Delivery Price Details
HOST_Escherichia coli (E. coli) Human His tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 1 mg Log in to see 29 to 34 Days
$4,331.68
Details
HOST_Escherichia coli (E. coli) Mouse His tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 1 mg Log in to see 29 to 34 Days
$4,331.68
Details
Insect Cells Mouse rho-1D4 tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 0.25 mg Log in to see 59 to 64 Days
$6,052.17
Details
Insect Cells Human rho-1D4 tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 0.5 mg Log in to see 59 to 64 Days
$8,623.45
Details

ANO5 Proteins by Origin and Source

Origin Expressed in Conjugate
Human ,
,
Mouse (Murine) ,
,

More Proteins for Anoctamin 5 (ANO5) Interaction Partners

Human Anoctamin 5 (ANO5) interaction partners

  1. Study screened the ANO5 gene in 786 myopathic patients and 52 controls by combining NGS and Sanger sequencing. In the cohort of patients, thirty-three are homozygous or compound heterozygous for causative mutations in ANO5

  2. supervised aerobic exercise training is safe and effective in improving oxidative capacity and muscle function in patients with anoctamin 5 deficiency

  3. The present report describes an association between LGMD2L consequent upon mutation in ANO5 and macular dystrophy in one affected person.

  4. Dilated cardiomyopathy is associated with mutations in the ANO5 gene.

  5. ANO5 mutations can be associated with amyloid deposition in muscle

  6. A high prevalence of ANO5 deficiency was found among patients with unclassified recessive limb girdle muscular dystrophy 2

  7. a diagnosis of ANO5 causing Muscular Dystrophy, Limb-Girdle, Type 2L, in 16% of the families (11/68) in a well-defined limb girdle muscular dystrophy cohort in the Netherlands

  8. investigated the prevalence and spectrum of ANO5 gene mutations and related clinical phenotypes; study confirmed that ANO5 gene mutations are responsible for about one fourth of cases of undiagnosed muscular dystrophy in the population studied

  9. This study showed that TMEM16E possesses distinct function other than chloride channel (show CLCA1 Proteins) activity, and another protein-stabilizing machinery toward the TMEM16E proteins should be considered for the on-set regulation of their phenotypes in tissues.

  10. By sequencing the entire ANO5 gene coding region and untranslated regions in a large Italian gnathodiaphyseal dyplasia family, a novel missense mutation causing the p.Thr513Ile substitution, was found.

Mouse (Murine) Anoctamin 5 (ANO5) interaction partners

  1. TMEM16E(-/-) sperm showed no apparent defect in morphology, beating, mitochondrial function, capacitation, or binding to zona pellucida. However, they showed reduced motility and inefficient fertilization of cumulus-free but zona-intact eggs in vitro.

  2. Ano5 mRNA and protein are widely expressed in the esophagus, stomach, duodenum, colon and rectum but Ano5 immunoreactivity are only detected in the mucosal layer, except for the muscular layer of the upper esophagus, which consists of skeletal muscle.

  3. characterized the complete cDNA sequence and genomic organization of the mouse GDD1 gene

  4. These observations suggest diverse cellular role(s) of GDD1 in the development of musculoskeletal system.

Anoctamin 5 (ANO5) Protein Profile

Protein Summary

This gene encodes a member of the anoctamin family of transmembrane proteins. The encoded protein is likely a calcium activated chloride channel. Mutations in this gene have been associated with gnathodiaphyseal dysplasia. Alternatively spliced transcript variants have been described.

Gene names and symbols associated with Anoctamin 5 Proteins (ANO5)

  • anoctamin 5 (ano5)
  • anoctamin 5 (ANO5)
  • anoctamin 5 (LOC100340377)
  • anoctamin 5a (ano5a)
  • anoctamin 5 (Ano5)
  • 9330162L24 protein
  • ano5 protein
  • Gdd1 protein
  • LGMD2L protein
  • MGC82557 protein
  • si:dkey-261m9.4 protein
  • Tmem16e protein

Protein level used designations for Anoctamin 5 Proteins (ANO5)

anoctamin 5 , transmembrane protein 16E , anoctamin-5 , anoctamin-5-like , tmem16ea , gnathodiaphyseal dysplasia 1 protein , integral membrane protein GDD1 , limb girdle muscular dystrophy 2L (autosomal recessive) , gnathodiaphyseal dysplasia 1 protein homolog

GENE ID SPECIES
446645 Xenopus laevis
485416 Canis lupus familiaris
100072055 Equus caballus
100140158 Bos taurus
100340377 Oryctolagus cuniculus
100389212 Callithrix jacchus
100459066 Pongo abelii
100484835 Ailuropoda melanoleuca
100534737 Danio rerio
100549161 Meleagris gallopavo
100567373 Anolis carolinensis
100587082 Nomascus leucogenys
100617099 Monodelphis domestica
203859 Homo sapiens
233246 Mus musculus
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