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: C3 ENSRNOG00000046834

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Description

complement C3 [Source:RGD Symbol;Acc:2232]

Location

Primary_assembly 9: 2,174,412-2,201,339 reverse strand.

GRCr8:CM070399.1

About this gene

This gene has 2 transcripts (splice variants), 556 orthologues, 12 paralogues and is associated with 124 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000075494.3	C3-202	5073	1663aa	ENSRNOP00000066934.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6KQR3 M0RBJ7	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,
ENSRNOT00000073042.5	C3-201	5034	1615aa	ENSRNOP00000066885.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	M0RBF1	-

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Summary

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