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
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: crygm2d21 ENSDARG00000086658

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Description

crystallin, gamma M2d21 [Source:ZFIN;Acc:ZDB-GENE-081105-133]

Gene Synonyms

si:ch211-212n6.16

Location

Chromosome 9: 22,298,246-22,299,412 reverse strand.

GRCz11:CM002893.2

About this gene

This gene has 2 transcripts (splice variants), 125 orthologues and 61 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000139101.2	crygm2d21-202	962	173aa	ENSDARP00000123536.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	B0S6N1	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,
ENSDART00000124600.3	crygm2d21-201	719	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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