Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Strains
Ontologies
- GO: Molecular function
- GO: Cellular component
- GO: Biological process
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: Mettl21a ENSRNOG00000014212

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Description

methyltransferase 21A, HSPA lysine [Source:RGD Symbol;Acc:7651604]

Gene Synonyms

Fam119a, LOC102553119, RGD1311824

Location

Primary_assembly 9: 73,471,813-73,481,339 reverse strand.

GRCr8:CM070399.1

About this gene

This gene has 1 transcript (splice variant), 205 orthologues and 5 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000019670.8	Mettl21a-201	1513	218aa	ENSRNOP00000019670.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D4A8Z5	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,

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Summary

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