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

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Gene: Dynlt2a2 ENSMUSG00000079710

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Description

dynein light chain Tctex-type 2A2 [Source:MGI Symbol;Acc:MGI:3809205]

Gene Synonyms

Dynlt2, Dynlt2b, Gm3448

Location

Chromosome 17: 15,216,078-15,230,444 reverse strand.

GRCm39:CM001010.3

About this gene

This gene has 2 transcripts (splice variants), 123 orthologues and 10 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	Flags
ENSMUST00000179539.9	Dynlt2a2-201	752	191aa	ENSMUSP00000137218.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS49961	A0A0R4J284	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, The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic, 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, TSL 1: A transcript where all splice junctions are supported by at least one non-suspect mRNA. The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users, based on the type and quality of the alignments used to annotate the transcript. TSL:1,
ENSMUST00000232299.2	Dynlt2a2-202	2253	49aa	ENSMUSP00000156126.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding		A0A338P777	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,

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Strains

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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