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Gene: METTL27 (methyltransferase like 27) Homo sapiens
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Symbol: METTL27
Name: methyltransferase like 27
Description: 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]
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: methyltransferase-like protein 27; MGC40131; WBSCR27; Williams Beuren syndrome chromosome region 27; Williams-Beuren syndrome chromosomal region 27 protein
Orthologs:
Mus musculus (house mouse) : Mettl27 (methyltransferase like 27)  MGI  Alliance
Rattus norvegicus (Norway rat) : Mettl27 (methyltransferase like 27)  Alliance
Chinchilla lanigera (long-tailed chinchilla) : Mettl27 (methyltransferase like 27)
Pan paniscus (bonobo/pygmy chimpanzee) : METTL27 (methyltransferase like 27)
Canis lupus familiaris (dog) : METTL27 (methyltransferase like 27)
Ictidomys tridecemlineatus (thirteen-lined ground squirrel) : Mettl27 (methyltransferase like 27)
Sus scrofa (pig) : METTL27 (methyltransferase like 27)
more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38773,834,590 - 73,842,527 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh37773,248,920 - 73,256,855 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36772,886,856 - 72,894,791 (-)NCBINCBI36hg18NCBI36
Build 34772,693,574 - 72,701,506NCBI
Celera768,727,572 - 68,735,487 (-)NCBI
Cytogenetic Map7q11.23NCBI
HuRef769,132,202 - 69,139,989 (-)NCBIHuRef
CHM1_1773,394,299 - 73,402,246 (-)NCBICHM1_1
CRA_TCAGchr7v2772,581,992 - 72,589,927 (-)NCBI
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
Gene-Chemical Interaction Annotations
Gene Ontology Annotations
References - curated
References - uncurated

Genomics

Comparative Map Data
miRNA Target Status

Expression


Sequence

Nucleotide Sequences
Protein Sequences
Promoters
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on METTL27
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 1352777
Created: 2005-03-08
Species: Homo sapiens
Last Modified: 2019-11-26
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.