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: WRN ENSSSCG00000015840

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Description

WRN RecQ like helicase [Source:VGNC Symbol;Acc:VGNC:96605]

Location

Primary_assembly 15: 53,966,986-54,094,587 reverse strand.

Sscrofa11.1:CM000826.5

About this gene

This gene has 6 transcripts (splice variants), 151 orthologues and 4 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000017248.3	WRN-202	4673	1466aa	ENSSSCP00000016786.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1RX70	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 ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2,
ENSSSCT00000043230.3	WRN-206	6627	1447aa	ENSSSCP00000033959.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A286ZQR4	APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. 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 P2,
ENSSSCT00000078835.1	WRN-205	5552	1403aa	ENSSSCP00000074284.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A5G2RAD7	APPRIS ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2,
ENSSSCT00000086771.2	WRN-204	5532	1342aa	ENSSSCP00000064524.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A5G2QKK9	-
ENSSSCT00000061430.3	WRN-203	5522	1403aa	ENSSSCP00000053814.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A287BB97	-
ENSSSCT00000056627.3	WRN-201	5314	1363aa	ENSSSCP00000052700.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A287B847	APPRIS ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2,

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Summary

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