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: MYLK4 ENSBTAG00000012079

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Description

myosin light chain kinase family member 4 [Source:VGNC Symbol;Acc:VGNC:31808]

Location

Primary_assembly 23: 50,879,655-50,947,103 forward strand.

ARS-UCD1.3:CM008190.2

About this gene

This gene has 3 transcripts (splice variants), 263 orthologues and 22 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000044315.5	MYLK4-202	1431	385aa	ENSBTAP00000041822.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1MG18	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,
ENSBTAT00000073098.2	MYLK4-201	2372	366aa	ENSBTAP00000063557.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1M5L3	-
ENSBTAT00000069993.2	MYLK4-203	1331	368aa	ENSBTAP00000065450.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1LXF9	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,

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Breeds

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Genomic alignments

Gene tree

Orthologues

Paralogues

Families (Not available)

More views of comparative genomics data, such as multiple alignments and synteny, are available on the Location page for this gene.

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Personal Data