SLC13A4 - solute carrier family 13 member 4 Gene
Also Known as NAS2; SUT1; SUT-1
Species: Homo sapiens
About SLC13A4
This gene has 8 transcripts (splice variants), 214 orthologues and 5 paralogues. Biased expression in placenta (RPKM 28.4) and testis (RPKM 3.0).
Summary
Predicted to enable sodium:sulfate symporter activity. Predicted to be involved in anion transmembrane transport. Predicted to be located in plasma membrane. Predicted to be integral component of plasma membrane. Predicted to be integral component of membrane. [provided by Alliance of Genome Resources, Apr 2022]
SLC13A4 Products (2)
| mRNA | Protein | Name |
|---|---|---|
| NM_001318192.2 | NP_001305121.1 | solute carrier family 13 member 4 isoform 1 |
| NM_012450.4 | NP_036582.2 | solute carrier family 13 member 4 isoform 2 |
| Molecular Function GO Annotation | Evidence | References | Source |
|---|---|---|---|
| enables protein binding |
IPI
IPI: Inferred from physical interaction
|
32296183 | GOA |
| enables sodium:sulfate symporter activity |
IDA
IDA: Inferred from direct assay
|
10535998 | GOA |
SLC13A4 Protein Structure
Na_sulph_symp: Sodium:sulfate symporter transmembrane region (12 - 609)
- 0
- 100
- 200
- 300
- 400
- 500
- 626 a.a.
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
solute carrier family 13 member 4 |
|
SLC13A4 Protein-protein interaction Information
|
Type
|
Protein Name | Protein ID | Interactor | Interactor Species | Interactor ID | Detection Method | References |
|---|---|---|---|---|---|---|---|
|
Intra
|
SLC13A4 | Q9UKG4 | CERS4 | Homo sapiens | Q9HA82 | 32296183 | |
|
Intra
|
SLC13A4 | Q9UKG4 | CERS4 | Homo sapiens | Q9HA82 | 32296183 | |
|
Intra
|
SLC13A4 | Q9UKG4 | GJA5 | Homo sapiens | P36382 | 32296183 | |
|
Intra
|
SLC13A4 | Q9UKG4 | GJA5 | Homo sapiens | P36382 | 32296183 | |
|
Intra
|
SLC13A4 | Q9UKG4 | CD79A | Homo sapiens | P11912 | 32296183 | |
|
Intra
|
SLC13A4 | Q9UKG4 | CD79A | Homo sapiens | P11912 | 32296183 |
Related Diseases
| Diseases | Alias | |
|---|---|---|
| Chondrodysplasia With Joint Dislocations, Gpapp Type |
|
|
| Developmental And Epileptic Encephalopathy 25 |
|
|
| Myopathy, Myosin Storage, Autosomal Dominant |
|
|
| Achondrogenesis, Type Ib |
|
|
| Schizophrenia 2 |
|
|
Orthologs Information
| Species | Symbol | Source | ID |
|---|---|---|---|
| Mus musculus | SLC13A4 | MGD | MGI:2442367 |
| Macaca mulatta | SLC13A4 | VGNC | VGNC:77489 |
| Felis catus | SLC13A4 | VGNC | VGNC:102703 |
| Canis familiaris | SLC13A4 | VGNC | VGNC:46230 |
| Bos taurus | SLC13A4 | VGNC | VGNC:34676 |
| Rattus norvegicus | SLC13A4 | RGD | RGD:1359715 |
| Others | SLC13A4 | NCBI |