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: HELQ ENSSSCG00000009236

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Description

helicase, POLQ like [Source:VGNC Symbol;Acc:VGNC:88839]

Location

Primary_assembly 8: 135,026,315-135,061,043 forward strand.

Sscrofa11.1:CM000819.5

About this gene

This gene has 2 transcripts (splice variants), 204 orthologues and 7 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000010115.4	HELQ-202	3483	1076aa	ENSSSCP00000009849.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8D0T696 F1RVE2	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,
ENSSSCT00000044598.3	HELQ-201	3253	1009aa	ENSSSCP00000034884.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A286ZTV7 A0A8D0TD67	-

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Paralogues

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