Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: CRYGF ENSBTAG00000052197

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Location

Primary_assembly 2: 97,070,871-97,073,823 forward strand.

ARS-UCD2.0:CM008169.2

About this gene

This gene has 2 transcripts (splice variants), 89 orthologues and 16 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000111443.1	CRYGF-201	674	192aa	ENSBTAP00000082946.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9SK28	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,
ENSBTAT00000018740.4	CRYGF-202	684	174aa	ENSBTAP00000018740.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	P23005	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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