Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
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: rex1bd ENSDARG00000073867

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Description

required for excision 1-B domain containing [Source:NCBI gene (formerly Entrezgene);Acc:564601]

Location

Chromosome 22: 21,167,096-21,176,269 reverse strand.

GRCz11:CM002906.2

About this gene

This gene has 2 transcripts (splice variants) and 93 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000112839.4	rex1bd-201	1083	170aa	ENSDARP00000102057.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	B8JL57	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,
ENSDART00000131743.3	rex1bd-202	840	170aa	ENSDARP00000113162.1	Nonsense mediated decay	B8JL57	-

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Summary

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