Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Cellular component
- GO: Biological process
- GO: Molecular function
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: CRYGC ENSPSNG00000021832

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Description

crystallin gamma C [Source:HGNC Symbol;Acc:HGNC:2410]

Location

Primary_assembly 7: 28,401,952-28,403,515 forward strand.

mPhoSin1.pri:CM018162.1

About this gene

This gene has 1 transcript (splice variant), 96 orthologues and 15 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPSNT00000033890.1	CRYGC-201	504	167aa	ENSPSNP00000030206.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8C9ECX9	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,

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Summary

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