2. Gene
  3. ASIC5 - acid sensing ion channel subunit family member 5 Gene

ASIC5 - acid sensing ion channel subunit family member 5 Gene

  • Gene
  • Protein
  • Disease
  • Agent
  • Ortholog
Homo sapiens

Also known as INAC; ACCN5; HINAC

Gene ID: 51802 | Gene type: protein coding

About ASIC5

Cytogenetic location: 4q32.1 Genomic coordinates (GRCh38): 4:155,829,729-155,866,277 (from NCBI)

This gene has 1 transcript (splice variant), 120 orthologues and 8 paralogues. Low expression observed in reference dataset.

Summary

This gene belongs to the amiloride-sensitive Na+ channel and degenerin (NaC/DEG) family, members of which have been identified in many animal species ranging from the nematode to human. The amiloride-sensitive Na(+) channel encoded by this gene is primarily expressed in the small intestine, however, its exact function is not known. [provided by RefSeq, Jul 2008]

ASIC5 Products(1)

mRNA Protein Name
NM_017419.3 NP_059115.1 acid-sensing ion channel 5

ASIC5 Protein Structure

ASC

ASC: Amiloride-sensitive sodium channel (41 - 467)

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  • 505 a.a.
Protein Preferred Names Protein Names

acid-sensing ion channel 5

acid sensing (proton gated) ion channel family member 5

Related Diseases

Diseases Alias
Pregnancy Loss, Recurrent 3

Pregnancy Loss, Recurrent, Susceptibility To, 3

RPRGL3

Pregnancy Loss, Recurrent, 3

Pregnancy Loss, Recurrent, Susceptibility To, Type 3
Pseudohypoaldosteronism
Liddle Syndrome 1

Liddle Syndrome

Pseudoaldosteronism

Liddle'S Syndrome

LIDLS1

Lidls

Pseudohyperaldosteronism

Pseudoprimary Hyperaldosteronism

Pseudohyperaldosteronism Type 1

Liddles Syndrome
Hyperpigmentation With Or Without Hypopigmentation, Familial Progressive

FPHH

Melanosis Universalis Hereditaria

Muh

Familial Progressive Hyperpigmentation With Or Without Hypopigmentation

Hyperpigmentation, Familial Progressive, 2, Formerly

Fph2, Formerly

Hyperpigmentation With Or Without Hypopigmentation

Familial Progressive Hyper- And Hypopigmentation

Hyperpigmentation, Familial Progressive
Ocular Albinism

Albinism, Ocular

Oa

Xloa

Albinism Ocular
Pseudohypoaldosteronism, Type I, Autosomal Recessive

Autosomal Recessive Pseudohypoaldosteronism Type 1

PHA1B

Pseudohypoaldosteronism Type 1

Pseudohypoaldosteronism, Type I

Generalized Pha1

Generalized Pseudohypoaldosteronism Type 1

Pseudohypoaldosteronism Type 1 Autosomal Recessive

Pha1

Pseudohypoaldosteronism

Pha I, Autosomal Recessive

Autosomal Recessive Pha 1

Pseudohypoaldosteronism Type 1, Recessive

Pseudohypoaldosteronism Type I

Autosomal Recessive Pha1

Pha Type 1

Pseudohypoaldosteronism 1, Autosomal Recessive

Multisystem Pseudohypoaldosteronism

Pha Type I, Autosomal Recessive

Pseudohypoaldosteronism Type I, Autosomal Recessive
Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Related Agents

Pre-clinical Phase
Bioactive Molecules (1)
Cat. No. Product Name Effect
Purity Rare Diseases
HY-RS01093 ASIC5 Human Pre-designed siRNA Set A / Unkown

Orthologs Information

Species Symbol Source ID
Mus musculus ASIC5 MGD MGI:1929259
Bos taurus ASIC5 VGNC VGNC:26213
Rattus norvegicus ASIC5 RGD RGD:69295
Canis familiaris ASIC5 VGNC VGNC:38181