FXYD7 - FXYD domain containing ion transport regulator 7 Gene
Species: Homo sapiens
About FXYD7
This gene has 4 transcripts (splice variants), 39 orthologues and 6 paralogues. Biased expression in brain (RPKM 25.1) and spleen (RPKM 0.7).
Summary
This reference sequence was derived from multiple replicate ESTs and validated by similar human genomic sequence. 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. 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. 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. This gene product, FXYD7, is novel and has not been characterized as a protein. [RefSeq curation by Kathleen J. Sweadner, Ph.D., [email protected]., Dec 2000]
FXYD7 Products (1)
| mRNA | Protein | Name |
|---|---|---|
| NM_022006.2 | NP_071289.1 | FXYD domain-containing ion transport regulator 7 |
| Molecular Function GO Annotation | Evidence | References | Source |
|---|---|---|---|
| enables protein binding |
IPI
IPI: Inferred from physical interaction
|
25416956 | GOA |
FXYD7 Protein Structure
ATP1G1_PLM_MAT8: ATP1G1/PLM/MAT8 family (13 - 59)
- 0
- 80 a.a.
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
FXYD domain-containing ion transport regulator 7 |
|
FXYD7 Protein-protein interaction Information
|
Type
|
Protein Name | Protein ID | Interactor | Interactor Species | Interactor ID | Detection Method | References |
|---|---|---|---|---|---|---|---|
|
Intra
|
FXYD7 | P58549 | SGTA | Homo sapiens | O43765 | 25416956 | |
|
Intra
|
FXYD7 | P58549 | SGTA | Homo sapiens | O43765 | 32296183 | |
|
Intra
|
FXYD7 | P58549 | SGTA | Homo sapiens | O43765 | 32296183 | |
|
Intra
|
FXYD7 | P58549 | SGTA | Homo sapiens | O43765 | 25416956 | |
|
Intra
|
FXYD7 | P58549 | SGTA | Homo sapiens | O43765 | 25416956 | |
|
Intra
|
FXYD7 | P58549 | APPBP2 | Homo sapiens | Q92624 | 32296183 | |
|
Intra
|
FXYD7 | P58549 | APPBP2 | Homo sapiens | Q92624 | 32296183 | |
|
Intra
|
FXYD7 | P58549 | APPBP2 | Homo sapiens | Q92624 | 32296183 | |
|
Intra
|
FXYD7 | P58549 | APPBP2 | Homo sapiens | Q92624 | 25416956 |
Related Diseases
| Diseases | Alias | |
|---|---|---|
| Hypomagnesemia 2, Renal |
|
|
Orthologs Information
| Species | Symbol | Source | ID |
|---|---|---|---|
| Rattus norvegicus | FXYD7 | RGD | RGD:620830 |
| Macaca mulatta | FXYD7 | VGNC | VGNC:107106 |
| Bos taurus | FXYD7 | VGNC | VGNC:29159 |
| Mus musculus | FXYD7 | MGD | MGI:1889006 |