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

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Gene: Rusf1 ENSRNOG00000020144

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Description

RUS family member 1 [Source:RGD Symbol;Acc:1310127]

Gene Synonyms

LOC361654, MGC124784, RGD1310127

Location

Primary_assembly 1: 192,282,711-192,311,137 reverse strand.

GRCr8:CM070391.1

About this gene

This gene has 2 transcripts (splice variants) and 187 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000113459.2	Rusf1-202	1520	495aa	ENSRNOP00000089500.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AL49	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,
ENSRNOT00000027290.7	Rusf1-201	2553	466aa	ENSRNOP00000027290.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6I9Z8 G3V8P5	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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