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

Gene: Rbmxl1b ENSRNOG00000059347

Description

Rbmx like 1B [Source:RGD Symbol;Acc:1585845]

Gene Synonyms

LOC680944, Rbmxl1, Rbmxrt

Location

GRCr8:CM070394.1

About this gene

This gene has 1 transcript (splice variant).

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	Flags
ENSRNOT00000081688.3	Rbmxl1b-201	1634	No protein	-	A gene that has homology to known protein-coding genes but contain a frameshift and/or stop codon(s) which disrupts the ORF. Thought to have arisen through duplication followed by loss of function.Pseudogene	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,

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