METTL27 - methyltransferase like 27 Gene

Also Known as WBSCR27

Species: Homo sapiens (human)

Gene Type: protein coding
Gene ID: 155368

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
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern
Protein Preferred Names Protein Names

methyltransferase-like protein 27

  • Williams Beuren syndrome chromosome region 27

  • williams-Beuren syndrome chromosomal region 27 protein

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
Cross: Cross-species interaction Intra: Intraspecies interaction