Summary
- Splice variants
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Sequence
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Comparative Genomics
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Gene: Rpf2 ENSRNOG00000000587

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Description

ribosome production factor 2 homolog [Source:RGD Symbol;Acc:1306906]

Gene Synonyms

Bxdc1, LOC294436

Location

Primary_assembly 20: 45,184,512-45,206,001 reverse strand.

GRCr8:CM070410.1

About this gene

This gene has 3 transcripts (splice variants) and 236 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000105691.2	Rpf2-203	1220	317aa	ENSRNOP00000079370.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZMX0	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,
ENSRNOT00000000717.9	Rpf2-201	1225	306aa	ENSRNOP00000000717.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AJR1 F7ENM1	APPRIS ALT1: 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 is conserved in at least 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 ALT1,
ENSRNOT00000095674.2	Rpf2-202	1147	280aa	ENSRNOP00000093895.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6KII4 B0BN82	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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Summary

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