Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Strains
  - Gene tree
  - Orthologues
  - Paralogues
Ontologies
- GO: Molecular function
- GO: Biological process
- GO: Cellular component
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: Crym ENSRNOG00000061215

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Description

crystallin, mu [Source:RGD Symbol;Acc:620943]

Gene Synonyms

CDK108, MGC108623

Location

Primary_assembly 1: 183,991,745-184,006,962 reverse strand.

GRCr8:CM070391.1

About this gene

This gene has 2 transcripts (splice variants), 202 orthologues and is associated with 3 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000095932.2	Crym-202	1377	356aa	ENSRNOP00000077282.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5Y7D3	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,
ENSRNOT00000088482.3	Crym-201	1248	313aa	ENSRNOP00000073313.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2K568 A6I8Q4 Q9QYU4	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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