1. Gene
  2. FXYD1 - FXYD domain containing ion transport regulator 1 Gene

FXYD1 - FXYD domain containing ion transport regulator 1 Gene

Homo sapiens

Also known as PLM

Gene ID: 5348 | Gene type: protein coding

About FXYD1

Cytogenetic location: 19q13.12 Genomic coordinates (GRCh38): 19:35,137,188-35,143,109 (from NCBI)

This gene has 11 transcripts (splice variants), 84 orthologues and 6 paralogues. Broad expression in liver (RPKM 47.5), heart (RPKM 45.3) and 14 other tissues.

Summary

This 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 for the family is FXYD-domain containing ion transport regulator. Mouse FXYD5 has been termed RIC (Related to Ion Channel). FXYD2, also known as the gamma subunit of the Na,K-ATPase, regulates the properties of that Enzyme. FXYD1 (phospholemman), FXYD2 (gamma), FXYD3 (MAT-8), FXYD4 (CHIF), and FXYD5 (RIC) have been shown to induce channel activity in experimental expression systems. Transmembrane topology has been established for two family members (FXYD1 and FXYD2), with the N-terminus extracellular and the C-terminus on the cytoplasmic side of the membrane. The protein encoded by this gene is a plasma membrane substrate for several kinases, including protein kinase A, protein kinase C, NIMA kinase, and myotonic dystrophy kinase. It is thought to form an ion channel or regulate ion channel activity. Transcript variants with different 5' UTR sequences have been described in the literature. [provided by RefSeq, Jul 2008]

FXYD1 Products(4)

mRNA Protein Name
NM_001278717.2 NP_001265646.1 phospholemman precursor
NM_001278718.2 NP_001265647.1 phospholemman precursor
NM_005031.5 NP_005022.2 phospholemman precursor
NM_021902.4 NP_068702.1 phospholemman precursor

FXYD1 Protein Structure

ATP1G1_PLM_MAT8

ATP1G1_PLM_MAT8: ATP1G1/PLM/MAT8 family (23 - 70)

  • 0
  • 92 a.a.
Protein Preferred Names Protein Names

phospholemman

sodium/potassium-transporting ATPase subunit FXYD1

Related Diseases

Diseases Alias
Rett Syndrome

Atypical Rett Syndrome

RTT

Rett Disorder

Rts

Autism, Dementia, Ataxia, And Loss Of Purposeful Hand Use

Rett Syndrome, Preserved Speech Variant

Rett Syndrome, Atypical

Rett'S Disorder

Rett Syndrome Variant

Autism-Dementia-Ataxia-Loss Of Purposeful Hand Use Syndrome

Cerebroatrophic Hyperammonemia

Rett Like Syndrome

Rett'S Syndrome

Atypical Rtt

Autism-Dementia-Ataxia-Loss Of Purposeful Hand Use

Rett Syndrome Preserved Speech Variant

Rett Syndrome Zappella Variant

Rett Syndrome, Zappella Variant

Alternating Hemiplegia Of Childhood

Alternating Hemiplegia

Ahc

Alternating Hemiplegia Syndrome

Hemiplegia, Alternating, Of Childhood

Hemiplegia, Crossed

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

Orthologs Information

Species Symbol Source ID
Bos taurus FXYD1 VGNC VGNC:29156
Mus musculus FXYD1 MGD MGI:1889273
Canis familiaris FXYD1 VGNC VGNC:41019
Rattus norvegicus FXYD1 RGD RGD:69306