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

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Gene: stim1b ENSDARG00000061560

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Description

stromal interaction molecule 1b [Source:ZFIN;Acc:ZDB-GENE-060531-4]

Gene Synonyms

si:ch211-112l17.2, stim1

Location

Chromosome 21: 30,841,241-30,935,262 reverse strand.

GRCz11:CM002905.2

About this gene

This gene has 2 transcripts (splice variants), 195 orthologues and 3 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000172390.2	stim1b-202	2575	668aa	ENSDARP00000131780.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0R4IAT9	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,
ENSDART00000142079.3	stim1b-201	2120	641aa	ENSDARP00000121917.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1R6G6	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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