| Name |
solute carrier family 35 member E1 |
laminin subunit alpha 3 |
| Structure |
No pdb structure
|
No pdb structure
|
| GO Annotations |
Cellular Component |
|
|
| Molecular Function |
|
|
| Biological Process |
|
|
| Pathways |
None
|
|
| Drugs |
None
|
|
| Diseases |
None
|
- Epidermolysis bullosa, junctional, including: Epidermolysis bullosa, junctional, Herlitz type (JEB-H); Epidermolysis bullosa, junctional, non-Herlitz type (JEB-nH); Epidermolysis bullosa, junctional, with pyloric atresia (JEB-PA)
- Laryngoonychocutaneous syndrome
- Epidermolysis bullosa, hemidesmosomal, including: Epidermolysis bullosa, generalized atrophic benign (GABEB); Epidermolysis bullosa simplex with pyloric atresia (EBS-PA); Epidermolysis bullosa simplex with muscular dystrophy (EBS-MD); Epidermolysis bullosa simplex, Ogna type (EBS-Ogna)
|
| GWAS |
No GWAS studies recorded
|
- Allergic rhinitis ( 25085501
)
- Amyotrophic lateral sclerosis ( 22959728
)
- Composite immunoglobulin trait (IgA x IgG/IgM) ( 28628107
)
- High light scatter reticulocyte count ( 27863252
)
- High light scatter reticulocyte percentage of red cells ( 27863252
)
|
| Interacting Genes |
6 interacting genes:
ABCF3
FTHL17
FXYD6
LAMA3
MCOLN1
MPP1
|
7 interacting genes:
APC
BMP1
LAMB3
PLAT
PLG
SDC2
SLC35E1
|
| Entrez ID |
79939 |
3909 |
| HPRD ID |
15373
|
02883
|
| Ensembl ID |
ENSG00000127526
|
ENSG00000053747
|
| Uniprot IDs |
Q96K37
|
A0A0A0MSA0
A0A0A0MTS5
A0A0A6YYF2
Q16787
|
| PDB IDs |
Not available
|
Not available
|
| GO Terms Enriched among Interactors |
|
|