Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
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: HELB ENSOCUG00000005909

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Description

DNA helicase B [Source:HGNC Symbol;Acc:HGNC:17196]

Location

Chromosome 4: 45,156,250-45,227,299 forward strand.

OryCun2.0:CM000793.1

About this gene

This gene has 2 transcripts (splice variants), 155 orthologues and 18 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSOCUT00000043355.1	HELB-202	3423	1140aa	ENSOCUP00000046855.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSOCUT00000005911.4	HELB-201	3279	1092aa	ENSOCUP00000005121.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	G1SPX9	-

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Summary

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