Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
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: Rfc2 ENSRNOG00000001457

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Description

replication factor C subunit 2 [Source:RGD Symbol;Acc:621198]

Gene Synonyms

MGC95315

Location

Primary_assembly 12: 27,756,922-27,770,025 reverse strand.

GRCr8:CM070402.1

About this gene

This gene has 2 transcripts (splice variants), 220 orthologues and 3 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000094282.2	Rfc2-202	1526	349aa	ENSRNOP00000077503.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6J0I4 Q641W4	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,
ENSRNOT00000001989.6	Rfc2-201	1466	329aa	ENSRNOP00000001989.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2Q0Z2	-

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Summary

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