FXYD4 Products

Description

The FXYD4 gene encodes a member of a family of small membrane proteins that share a 35-amino acid signature sequence domain, beginning with the sequence PFXYD and containing 7 invariant and 6 highly conserved amino acids. The approved human gene nomenclature f

Bioinformatics

Entrez	53828 Human
Uniprot	P59646 Human NM_173160 Human
Product By Gene ID	53828
Alternate Names	channel-inducing factor FXYD domain-containing ion transport regulator 4 CHIF FXYD domain containing ion transport regulator 4

Diseases related to FXYD4

Discover more about diseases related to FXYD4.

Disease Of Adrenal Medulla
Acidosis
Kidney Failure
Reperfusion Injury
Ischemia
Kidney Failure, Acute
Acute Kidney Injury
Neoplasms
Renal Ischaemia
Ischemic Reperfusion Injury
Kidney Tubular Necrosis, Acute
Salivary Gland Diseases
Macule
Metabolic Acidosis
Hypertensive Disease
Mammary Neoplasms
Shwachman Syndrome
Multiple Acyl Coenzyme A Dehydrogenase Deficiency

Pathways for FXYD4

View related products by pathway and learn more about each of the pathways below.

Transport
Ion Transport
Excretion
Renal Potassium Excretion
Cellular Homeostasis
Glycosylation
Muscle Contraction
Protein Unfolding
Localization
Membrane Depolarization
Cellular Localization
Protein Denaturation
Tubuloglomerular Feedback
Secretion

PTMs for FXYD4

Learn more about PTMs related to FXYD4.

Phosphorylation
Glycosylation

Bioinformatics Tool for FXYD4

Discover related pathways, diseases and genes to FXYD4. Need help? Read the Bioinformatics Tool Guide for instructions on using this tool.