autosomal recessive pseudohypoaldosteronism type 1

Summary
Synonym
  • PHA1B
  • autosomal recessive PHA 1
Definition
A pseudohypoaldosteronism characterized by enal salt wasting and high concentrations of sodium in sweat, stool, and saliva that has_material_basis_in homozygous or compound heterozygous mutation in any one of 3 genes encoding subunits of the epithelial sodium channel (ENaC): SCNN1A, SCNN1B, or SCNN1G.
Super Class
autosomal recessive disease pseudohypoaldosteronism
Disease Ontology
DOID:0060854
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
ORDO
OMIM
GARD
MGI genotype (from TogoID)
Related Genes
Displaying all 2 entries
Gene ID Gene Symbol Description Source
6338 SCNN1B sodium channel epithelial 1 subunit beta
6340 SCNN1G sodium channel epithelial 1 subunit gamma
Displaying all 2 entries
Gene ID Gene Symbol Description Source
20277 Scnn1b sodium channel, nonvoltage-gated 1 beta
20278 Scnn1g sodium channel, nonvoltage-gated 1 gamma
Displaying all 2 entries
Gene ID Gene Symbol Description Source
24767 Scnn1b sodium channel epithelial 1 subunit beta
24768 Scnn1g sodium channel epithelial 1 subunit gamma
Displaying all 6 entries
Gene ID Gene Symbol Description Source
174306 unc-105 Degenerin-like protein unc-105
177494 unc-8 Degenerin unc-8
181035 deg-1 Degenerin deg-1
181101 mec-10 Degenerin mec-10
181728 mec-4 Degenerin mec-4
191422 asic-1 Degenerin-like protein asic-1

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024