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

Configure this page

Share this page

Bookmark this page

.

Gene: C2cd2l ENSRNOG00000009719

.

Description

C2CD2-like [Source:RGD Symbol;Acc:1310281]

Gene Synonyms

LOC300666, Tmem24

Location

Primary_assembly 8: 53,544,892-53,555,153 reverse strand.

GRCr8:CM070398.1

About this gene

This gene has 2 transcripts (splice variants), 194 orthologues, 1 paralogue and is associated with 13 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000030745.8	C2cd2l-201	3339	708aa	ENSRNOP00000036065.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F7EUW3	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,
ENSRNOT00000083490.3	C2cd2l-202	3350	663aa	ENSRNOP00000072391.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2K2V4	-

.

Summary

.

.