Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: Rbm39 ENSRNOG00000019848

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Description

RNA binding motif protein 39 [Source:RGD Symbol;Acc:1310071]

Gene Synonyms

LOC100910882, LOC362251, MGC109490, Rnp1, Rnpc2, Rrm

Location

Primary_assembly 3: 165,123,095-165,149,397 reverse strand.

GRCr8:CM070393.1

About this gene

This gene has 1 transcript (splice variant), 299 orthologues and 35 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000026964.9	Rbm39-201	2496	487aa	ENSRNOP00000026964.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6A9I1 A0A8J8XIU8	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,

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Summary

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