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

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Gene: SEPTIN11 ENSBTAG00000021372

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Description

septin 11 [Source:VGNC Symbol;Acc:VGNC:34451]

Gene Synonyms

SEPT11

Location

Primary_assembly 6: 91,737,476-91,876,735 forward strand.

ARS-UCD2.0:CM008173.2

About this gene

This gene has 9 transcripts (splice variants), 140 orthologues and 13 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000068737.3	SEPTIN11-202	1643	470aa	ENSBTAP00000058615.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1MUN6	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,
ENSBTAT00000142306.1	SEPTIN11-203	8873	425aa	ENSBTAP00000107618.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	APPRIS ALT1: 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 is conserved in at least 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 ALT1,
ENSBTAT00000142562.1	SEPTIN11-208	8697	420aa	ENSBTAP00000105718.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSBTAT00000135021.2	SEPTIN11-207	5583	428aa	ENSBTAP00000085636.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9SHF5	-
ENSBTAT00000099106.2	SEPTIN11-201	5497	427aa	ENSBTAP00000083065.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9SKD2	-
ENSBTAT00000005626.7	SEPTIN11-206	5480	426aa	ENSBTAP00000005626.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A452DIM2 A0AAA9SIW8	-
ENSBTAT00000133801.2	SEPTIN11-209	5349	388aa	ENSBTAP00000099784.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9TR55	-
ENSBTAT00000075617.3	SEPTIN11-205	2589	432aa	ENSBTAP00000063083.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAF7A4F2	APPRIS ALT1: 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 is conserved in at least 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 ALT1,
ENSBTAT00000076166.3	SEPTIN11-204	2190	429aa	ENSBTAP00000066044.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1LZ10	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,

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Summary

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