Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: hel-1 WBGene00001840

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Description

Spliceosome RNA helicase DDX39B homolog [Source:NCBI gene (formerly Entrezgene);Acc:174333]

Location

Chromosome II: 8,326,852-8,328,870 reverse strand.

WBcel235:BX284602.5

About this gene

This gene has 2 transcripts (splice variants), 287 orthologues and 30 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
C26D10.2a.1	hel-1-201	1522	425aa	C26D10.2a.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q18212	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,
C26D10.2b	hel-1-202	1594	No protein	-	A non-coding gene.ncRNA	-	-

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Summary

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