Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
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: Recql4 ENSRNOG00000032446

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Description

RecQ like helicase 4 [Source:RGD Symbol;Acc:1307732]

Location

Primary_assembly 7: 110,304,094-110,311,258 reverse strand.

GRCr8:CM070397.1

About this gene

This gene has 2 transcripts (splice variants), 161 orthologues, 4 paralogues and is associated with 16 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000129887.1	Recql4-202	3929	1239aa	ENSRNOP00000099781.1	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,
ENSRNOT00000045135.6	Recql4-201	3863	1217aa	ENSRNOP00000047177.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D4A5W5	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,

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Summary

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