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

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Gene: SPIB ENSBTAG00000043953

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Description

Spi-B transcription factor [Source:NCBI gene (formerly Entrezgene);Acc:784460]

Gene Synonyms

B42b-like

Location

Primary_assembly 18: 56,572,529-56,580,057 forward strand.

ARS-UCD2.0:CM008185.2

About this gene

This gene has 2 transcripts (splice variants), 98 orthologues and 28 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000061114.5	SPIB-201	3124	261aa	ENSBTAP00000053467.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1MMZ5	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,
ENSBTAT00000111938.2	SPIB-202	2195	171aa	ENSBTAP00000087152.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9SP55	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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