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

Gene: Eef1akmt1 ENSRNOG00000009849

Description

EEF1A lysine methyltransferase 1 [Source:RGD Symbol;Acc:1306762]

Gene Synonyms

LOC290279, MGC188401, N6amt2, RGD1306762

Location

Primary_assembly 15: 31,694,292-31,711,336 reverse strand.

mRatBN7.2:CM026988.1

About this gene

This gene has 3 transcripts (splice variants), 205 orthologues and is associated with 7 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000075861.3	Eef1akmt1-202	1023	224aa	ENSRNOP00000068470.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A096MKD1	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 ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2,
ENSRNOT00000064702.4	Eef1akmt1-201	881	224aa	ENSRNOP00000059566.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F7FGJ4	APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. 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 P2,
ENSRNOT00000075884.2	Eef1akmt1-203	654	58aa	ENSRNOP00000068357.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A096MK28	-

Gene: Eef1akmt1 ENSRNOG00000009849

Summary

About Us

Get help

Our sister sites

Follow us

Favourite species

All species

Recent locations

Gene: Eef1akmt1 ENSRNOG00000009849

Summary

About Us

Get help

Our sister sites

Follow us