Gene: Mylk3 ENSRNOG00000017546

Description

myosin light chain kinase 3 [Source:RGD Symbol;Acc:1305801]

Gene Synonyms

LOC291926, MLCK, RGD1305801

Location

Primary_assembly 19: 21,691,929-21,742,954 forward strand.

mRatBN7.2:CM026992.1

About this gene

This gene has 3 transcripts (splice variants), 150 orthologues, 21 paralogues and is associated with 3 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000023657.7	Mylk3-201	2732	786aa	ENSRNOP00000023657.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E9PT87	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 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,
ENSRNOT00000119434.1	Mylk3-203	4307	737aa	ENSRNOP00000090047.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6GIK4	-
ENSRNOT00000100814.1	Mylk3-202	2158	653aa	ENSRNOP00000083206.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZYT9	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,