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

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Gene: MOS ENSBTAG00000019145

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Description

MOS proto-onco, serine/threonine kinase [Source:VGNC Symbol;Acc:VGNC:31563]

Location

Primary_assembly 14: 23,294,743-23,300,688 reverse strand.

ARS-UCD2.0:CM008181.2

About this gene

This gene has 2 transcripts (splice variants), 173 orthologues and 23 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000101459.1	MOS-202	2122	345aa	ENSBTAP00000086977.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9SNP6	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 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,
ENSBTAT00000025483.6	MOS-201	1623	340aa	ENSBTAP00000025483.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F6RCH9	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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