Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Breeds
  - Gene tree
  - Orthologues
  - Paralogues
Ontologies
- GO: Molecular function
- GO: Biological process
- GO: Cellular component
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: REX1BD ENSBTAG00000007739

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Description

required for excision 1-B domain containing [Source:VGNC Symbol;Acc:VGNC:52875]

Location

Primary_assembly 7: 4,598,864-4,602,133 reverse strand.

ARS-UCD1.3:CM008174.2

About this gene

This gene has 3 transcripts (splice variants) and 80 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000036534.4	REX1BD-202	759	201aa	ENSBTAP00000036391.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q17Q97	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,
ENSBTAT00000110473.1	REX1BD-203	1400	182aa	ENSBTAP00000100793.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSBTAT00000084688.2	REX1BD-201	1339	162aa	ENSBTAP00000062591.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1LYE1	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,

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Breeds

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Genomic alignments

Gene tree

Orthologues

Paralogues (Not available)

Families (Not available)

More views of comparative genomics data, such as multiple alignments and synteny, are available on the Location page for this gene.

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Personal Data