Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: LIMK2 ENSBTAG00000010662

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Description

LIM domain kinase 2 [Source:VGNC Symbol;Acc:VGNC:52793]

Location

Primary_assembly 17: 70,038,756-70,093,299 forward strand.

ARS-UCD2.0:CM008184.2

About this gene

This gene has 4 transcripts (splice variants), 204 orthologues and 23 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000068530.3	LIMK2-203	3214	640aa	ENSBTAP00000068583.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1MHL3 F1MGL9	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,
ENSBTAT00000086598.3	LIMK2-201	3674	617aa	ENSBTAP00000058653.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1LNS0	-
ENSBTAT00000079813.3	LIMK2-202	3666	628aa	ENSBTAP00000071696.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1ML60	-
ENSBTAT00000068535.3	LIMK2-204	3503	617aa	ENSBTAP00000073941.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1MTZ9	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,

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Summary

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