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

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Gene: CRYGS ENSG00000213139

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Description

crystallin, gamma S [Source:HGNC Symbol;Acc:2417]

Gene Synonyms

CRYG8, CTRCT20

Location

Chromosome 3: 186,256,230-186,264,491 reverse strand.

GRCh37:CM000665.1

About this gene

This gene has 3 transcripts (splice variants), 11 paralogues and is associated with 4 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000392499.2	CRYGS-001	1132	178aa	ENSP00000376287.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS3275	P22914 Q9UFA7	NM_017541.2	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000307944.5	CRYGS-002	759	178aa	ENSP00000312099.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS3275	P22914 Q9UFA7	-	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000460288.1	CRYGS-003	1536	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron		-	-	-

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Summary

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