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

Configure this page

Share this page

Bookmark this page

.

Gene: ATOSB ENSBTAG00000011394

.

Description

atos homolog B [Source:VGNC Symbol;Acc:VGNC:28794]

Gene Synonyms

FAM214B

Location

Primary_assembly 8: 59,362,626-59,373,750 reverse strand.

ARS-UCD2.0:CM008175.2

About this gene

This gene has 3 transcripts (splice variants), 202 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000015139.4	ATOSB-203	2594	538aa	ENSBTAP00000015139.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q5BIM2	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,
ENSBTAT00000073509.2	ATOSB-201	2768	488aa	ENSBTAP00000066676.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAF7AC72	-
ENSBTAT00000126689.1	ATOSB-202	2400	500aa	ENSBTAP00000076010.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9RUX0	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,

.

Summary

.

.