Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Breeds
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: RFC3 ENSBTAG00000010787

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Description

replication factor C subunit 3 [Source:VGNC Symbol;Acc:VGNC:33887]

Location

Primary_assembly 12: 27,328,055-27,396,140 reverse strand.

ARS-UCD2.0:CM008179.2

About this gene

This gene has 2 transcripts (splice variants), 206 orthologues and 3 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000098202.1	RFC3-201	1199	375aa	ENSBTAP00000099727.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9TML2	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,
ENSBTAT00000014278.5	RFC3-202	1200	356aa	ENSBTAP00000014278.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q2TBV1	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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