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: SRMS ENSBTAG00000001985

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Description

src-related kinase lacking C-terminal regulatory tyrosine and N-terminal myristylation sites [Source:VGNC Symbol;Acc:VGNC:35283]

Location

Primary_assembly 13: 54,119,425-54,127,541 forward strand.

ARS-UCD2.0:CM008180.2

About this gene

This gene has 1 transcript (splice variant), 143 orthologues and 32 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000002574.8	SRMS-201	3842	494aa	ENSBTAP00000002574.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1N1Q0	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 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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