METTL27 - methyltransferase like 27 Gene
Also Known as WBSCR27
Species: Homo sapiens (human)
Summary
This gene encodes a protein belonging to ubiE/COQ5 methyltransferase family. The gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.22-q11.23. [provided by RefSeq, Jul 2008]
METTL27 Products (1)
| mRNA | Protein | Name |
|---|---|---|
| XM_017011778.2 | XP_016867267.1 | methyltransferase-like protein 27 isoform X1 |
| Molecular Function GO Annotation | Evidence | References | Source |
|---|---|---|---|
| enables protein binding |
IPI
IPI: Inferred from physical interaction
|
25814554 | GOA |
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
methyltransferase-like protein 27 |
|
METTL27 Protein-protein interaction Information
|
Type
|
Protein Name | Protein ID | Interactor | Interactor Species | Interactor ID | Detection Method | References |
|---|---|---|---|---|---|---|---|
|
Intra
|
METTL27 | Q8N6F8 | A1CF | Homo sapiens | Q9NQ94 | 32296183 | |
|
Intra
|
METTL27 | Q8N6F8 | TFG | Homo sapiens | Q92734 | 32296183 | |
|
Intra
|
METTL27 | Q8N6F8 | FOXC2 | Homo sapiens | Q99958 | 32296183 | |
|
Intra
|
METTL27 | Q8N6F8 | ENKD1 | Homo sapiens | Q9H0I2 | 32296183 | |
|
Intra
|
METTL27 | Q8N6F8 | CCDC120 | Homo sapiens | Q96HB5 | 32296183 | |
|
Intra
|
METTL27 | Q8N6F8 | PRPS1 | Homo sapiens | P60891 | 32814053 | |
|
Intra
|
METTL27 | Q8N6F8 | PRPS1 | Homo sapiens | P60891 | 32814053 | |
|
Intra
|
METTL27 | Q8N6F8 | PRPS1 | Homo sapiens | P60891 | 32814053 | |
|
Intra
|
METTL27 | Q8N6F8 | PIK3R3 | Homo sapiens | Q92569 | 25814554 | |
|
Intra
|
METTL27 | Q8N6F8 | PIK3R3 | Homo sapiens | Q92569 | 25814554 | |
|
Intra
|
METTL27 | Q8N6F8 | TEKT3 | Homo sapiens | Q9BXF9 | 32296183 |