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: CECR1 ENSGALG00010011860

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Description

cat eye syndrome chromosome region, candidate 1 [Source:NCBI gene (formerly Entrezgene);Acc:418160]

Gene Synonyms

ADA2

Location

Primary_assembly 1: 61,711,482-61,730,279 reverse strand.

bGalGal1.mat.broiler.GRCg7b:CM028482.1

About this gene

This gene has 2 transcripts (splice variants), 243 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSGALT00010028327.1	CECR1-202	2536	519aa	ENSGALP00010016229.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1NML7	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,
ENSGALT00010028337.1	CECR1-201	4988	481aa	ENSGALP00010016238.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8V0YEW0	-

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Summary

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