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

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Gene: stmn1b ENSDARG00000033655

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Description

stathmin 1b [Source:ZFIN;Acc:ZDB-GENE-050417-397]

Gene Synonyms

fj38b07, fj43c10, stathmin 1/oncoprotein 18b, wu:fj38b07, wu:fj43c10, zgc:110159

Location

Chromosome 16: 34,523,515-34,527,206 forward strand.

GRCz11:CM002900.2

About this gene

This gene has 1 transcript (splice variant), 256 orthologues and 7 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000041007.7	stmn1b-201	1687	149aa	ENSDARP00000041006.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q568Q7	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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