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

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Gene: Crygf ENSRNOG00000032869

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Description

crystallin, gamma F [Source:RGD Symbol;Acc:1586353]

Gene Synonyms

Cryg6, Crygf_mapped, LOC689947, Len

Location

Primary_assembly 9: 74,897,673-74,900,148 forward strand.

GRCr8:CM070399.1

About this gene

This gene has 2 transcripts (splice variants), 31 orthologues and 16 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000114566.2	Crygf-202	613	182aa	ENSRNOP00000091547.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AGB7	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,
ENSRNOT00000041632.5	Crygf-201	684	174aa	ENSRNOP00000045818.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6KFC0 G3V9F6	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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