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: st14b ENSDARG00000044655

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Description

suppression of tumorigenicity 14b [Source:ZFIN;Acc:ZDB-GENE-061103-613]

Gene Synonyms

matriptase 1b, zgc:152947

Location

Chromosome 21: 25,275,693-25,295,087 reverse strand.

GRCz11:CM002905.2

About this gene

This gene has 2 transcripts (splice variants), 901 orthologues and 16 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000147860.2	st14b-202	3008	864aa	ENSDARP00000119901.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E9QD17	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,
ENSDART00000087910.6	st14b-201	2678	753aa	ENSDARP00000082343.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1QNJ6	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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