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: slx4 ENSDARG00000061414

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Location

Chromosome 22: 26,798,853-26,844,334 forward strand.

GRCz11:CM002906.2

About this gene

This gene has 3 transcripts (splice variants), 208 orthologues, 1 paralogue and is associated with 11 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000087576.6	slx4-201	5452	1719aa	ENSDARP00000082010.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1QPU2	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,
ENSDART00000179780.1	slx4-203	5431	1712aa	ENSDARP00000152101.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSDART00000147719.2	slx4-202	623	208aa	ENSDARP00000122025.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	5' and 3' truncations in transcript evidence prevent annotation of the start and the end of the CDS.CDS 5' and 3' incomplete,

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Summary

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