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: UNC13B ENSSSCG00000005305

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Description

unc-13 homolog B [Source:VGNC Symbol;Acc:VGNC:103199]

Location

Primary_assembly 1: 235,918,747-236,158,098 forward strand.

Sscrofa11.1:CM000812.5

About this gene

This gene has 4 transcripts (splice variants), 201 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000084499.2	UNC13B-202	14447	4266aa	ENSSSCP00000067794.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A5G2QUF9	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,
ENSSSCT00000055365.3	UNC13B-201	7468	1988aa	ENSSSCP00000059304.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A287BRN3	-
ENSSSCT00000065284.3	UNC13B-204	6518	1621aa	ENSSSCP00000031717.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A286ZJK8	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,
ENSSSCT00000037962.3	UNC13B-203	6471	1611aa	ENSSSCP00000058861.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A287BQS1	APPRIS P4: Where the APPRIS core modules are unable to choose a clear principal CDS and there is more than one variant with a distinct (but consecutive) CCDS identifiers, APPRIS selects the longest CCDS isoform 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 P4,

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Summary

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