Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Molecular function
- GO: Biological process
- GO: Cellular component
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: mettl27 ENSDARG00000069507

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Description

methyltransferase like 27 [Source:ZFIN;Acc:ZDB-GENE-060421-5918]

Gene Synonyms

Williams Beuren syndrome chromosome region 27, im:7139431, wbscr27, wu:fe50c11, zgc:136279

Location

Chromosome 21: 25,795,875-25,801,956 reverse strand.

GRCz11:CM002905.2

About this gene

This gene has 2 transcripts (splice variants), 232 orthologues and 11 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000101219.5	mettl27-201	1327	235aa	ENSDARP00000091993.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1QE45	A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical, APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P1,
ENSDART00000122344.3	mettl27-202	900	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron	-	-

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Summary

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