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: Cellular component
- GO: Biological process
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: Chlsn ENSRNOG00000001289

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Description

cholesin [Source:RGD Symbol;Acc:1566418]

Gene Synonyms

C12h7orf50, C7orf50, LOC498154

Location

Primary_assembly 12: 20,388,520-20,402,922 forward strand.

GRCr8:CM070402.1

About this gene

This gene has 2 transcripts (splice variants) and 175 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000001734.7	Chlsn-201	1655	224aa	ENSRNOP00000001734.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q5I0E3	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,
ENSRNOT00000101891.2	Chlsn-202	1640	206aa	ENSRNOP00000092701.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AIG4	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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