Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
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  - Gene tree
  - Orthologues
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Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
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- Structural variants
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Molecular interactions
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ID History
- Gene history

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Gene: Csn2 ENSRNOG00000039326

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Description

casein beta [Source:RGD Symbol;Acc:61981]

Gene Synonyms

Csn 2, Csnb

Location

Primary_assembly 14: 20,601,824-20,609,060 forward strand.

GRCr8:CM070404.1

About this gene

This gene has 3 transcripts (splice variants), 86 orthologues and is associated with 3 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000150843.1	Csn2-203	745	231aa	ENSRNOP00000103172.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6KU20	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,
ENSRNOT00000060265.5	Csn2-201	1060	230aa	ENSRNOP00000057016.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	G3V9R5	APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. 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 P2,
ENSRNOT00000098581.2	Csn2-202	1015	215aa	ENSRNOP00000089457.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6ABZ4	APPRIS ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2,

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Summary

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