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
External references
Supporting evidence
ID History
- Gene history

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Gene: Csn1s2b ENSRNOG00000055083

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Description

casein alpha s2-like B [Source:RGD Symbol;Acc:628794]

Gene Synonyms

Csnd

Location

Primary_assembly 14: 20,529,498-20,545,749 reverse strand.

GRCr8:CM070404.1

About this gene

This gene has 4 transcripts (splice variants), 15 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000143958.1	Csn1s2b-203	752	169aa	ENSRNOP00000102145.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSRNOT00000160686.1	Csn1s2b-204	913	161aa	ENSRNOP00000111249.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000087672.3	Csn1s2b-201	662	139aa	ENSRNOP00000068969.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2JU53	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,
ENSRNOT00000088024.3	Csn1s2b-202	629	128aa	ENSRNOP00000074666.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2K8M6	-

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Summary

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