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: ddx39b ENSDARG00000036069

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Description

DEAD (Asp-Glu-Ala-Asp) box polypeptide 39B [Source:NCBI gene (formerly Entrezgene);Acc:393917]

Location

Chromosome 19: 27,339,848-27,358,545 forward strand.

GRCz11:CM002903.2

About this gene

This gene has 3 transcripts (splice variants), 156 orthologues and 38 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000052355.6	ddx39b-201	1928	435aa	ENSDARP00000052354.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q7SXU7	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 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,
ENSDART00000184687.1	ddx39b-203	2708	435aa	ENSDARP00000144813.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q7SXU7	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,
ENSDART00000149515.2	ddx39b-202	413	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron	-	-

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Summary

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