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
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: Crygd ENSRNOG00000032219

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Description

crystallin, gamma D [Source:RGD Symbol;Acc:2422]

Gene Synonyms

Cryg4, Len

Location

Primary_assembly 9: 73,935,795-73,937,808 reverse strand.

GRCr8:CM070399.1

About this gene

This gene has 2 transcripts (splice variants), 19 orthologues, 16 paralogues and is associated with 12 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000107623.2	Crygd-202	601	176aa	ENSRNOP00000082230.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZXH9	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,
ENSRNOT00000050886.4	Crygd-201	634	174aa	ENSRNOP00000051301.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6IPJ1 P10067	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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