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
Phenotypes
Genetic Variation
- Variant table
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Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: Ctnnbl1 ENSRNOG00000012021

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Description

catenin, beta like 1 [Source:RGD Symbol;Acc:1563558]

Gene Synonyms

NAP

Location

Primary_assembly 3: 146,387,889-146,548,987 forward strand.

mRatBN7.2:CM026976.1

About this gene

This gene has 3 transcripts (splice variants), 218 orthologues and is associated with 6 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000099751.1	Ctnnbl1-202	1887	570aa	ENSRNOP00000092969.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AHN5	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,
ENSRNOT00000066808.4	Ctnnbl1-201	1892	564aa	ENSRNOP00000060192.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2QUN4	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,
ENSRNOT00000117662.1	Ctnnbl1-203	1765	556aa	ENSRNOP00000084879.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6A264	-

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Strains

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Genomic alignments

Gene tree

Orthologues

Paralogues (Not available)

Families (Not available)

More views of comparative genomics data, such as multiple alignments and synteny, are available on the Location page for this gene.

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Personal Data