Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
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: C2CD2L ENSPTRG00000004371

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Description

C2CD2 like [Source:VGNC Symbol;Acc:VGNC:6760]

Location

Chromosome 11: 119,575,618-119,586,013 forward strand.

Pan_tro_3.0:CM000325.3

About this gene

This gene has 2 transcripts (splice variants), 194 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000078233.1	C2CD2L-202	2136	711aa	ENSPTRP00000064504.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3RIN9	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,
ENSPTRT00000008113.5	C2CD2L-201	4012	707aa	ENSPTRP00000040890.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2YBU4 H2R0L2	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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