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

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Gene: mettl27 ENSPNYG00000017463

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Description

Williams-Beuren syndrome chromosomal region 27 protein-like [Source:NCBI gene;Acc:102211010]

Location

Primary_assembly JH419768.1: 134,032-136,315 forward strand.

About this gene

This gene has 1 transcript (splice variant), 179 orthologues and 11 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPNYT00000023696.1	mettl27-201	621	206aa	ENSPNYP00000023129.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3B4GLS0	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,

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Summary

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