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
External references
Supporting evidence
ID History
- Gene history

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Gene: C5l1 ENSRNOG00000022033

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Description

complement C5 like 1 [Source:RGD Symbol;Acc:1308742]

Gene Synonyms

LOC362120, RGD1308742

Location

Primary_assembly 3: 38,799,731-38,817,527 reverse strand.

GRCr8:CM070393.1

About this gene

This gene has 2 transcripts (splice variants), 193 orthologues and 12 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000127215.1	C5l1-202	1047	348aa	ENSRNOP00000105153.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSRNOT00000035829.7	C5l1-201	1035	345aa	ENSRNOP00000082846.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6GA02	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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