Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Molecular function
- GO: Biological process
- GO: Cellular component
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: chrm1a ENSDARG00000037292

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Description

cholinergic receptor, muscarinic 1a [Source:ZFIN;Acc:ZDB-GENE-090410-9]

Location

Chromosome 14: 24,258,562-24,262,815 forward strand.

GRCz11:CM002898.2

About this gene

This gene has 2 transcripts (splice variants), 101 orthologues and 149 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000173227.2	chrm1a-202	1422	465aa	ENSDARP00000142274.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A140LG95	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, APPRIS P5: Where the APPRIS core modules are unable to choose a clear principal variant and none of the candidate variants are annotated by CCDS, APPRIS selects the longest of the candidate isoforms as 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 P5,
ENSDART00000106074.5	chrm1a-201	1245	414aa	ENSDARP00000096852.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E7F3K3	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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