ASIC5 - acid sensing ion channel subunit family member 5 Gene

Also Known as INAC; ACCN5; HINAC

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 51802

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)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 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

Pre-clinical Phase

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