Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
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: Cryl1 ENSRNOG00000008989

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Description

crystallin, lambda 1 [Source:RGD Symbol;Acc:631427]

Gene Synonyms

gul3DH

Location

Primary_assembly 15: 31,427,054-31,545,997 reverse strand.

mRatBN7.2:CM026988.1

About this gene

This gene has 2 transcripts (splice variants), 204 orthologues, 3 paralogues and is associated with 10 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000094908.1	Cryl1-202	1359	321aa	ENSRNOP00000083620.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZZK9	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,
ENSRNOT00000012093.4	Cryl1-201	1416	319aa	ENSRNOP00000012093.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q811X6	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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