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

Configure this page

Share this page

Bookmark this page

.

Gene: Clgn ENSRNOG00000003755

.

Description

calmegin [Source:RGD Symbol;Acc:1592643]

Gene Synonyms

LOC685504

Location

Primary_assembly 19: 41,601,568-41,633,325 reverse strand.

GRCr8:CM070409.1

About this gene

This gene has 2 transcripts (splice variants), 196 orthologues, 4 paralogues and is associated with 1 phenotype.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000005071.7	Clgn-201	2277	612aa	ENSRNOP00000005071.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZFS2	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,
ENSRNOT00000103637.2	Clgn-202	2242	564aa	ENSRNOP00000093435.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6GKA5	-

.

Summary

.

.