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

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Gene: Septin12 ENSRNOG00000003137

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Description

septin 12 [Source:RGD Symbol;Acc:1565511]

Gene Synonyms

LOC363542, Sept12

Location

Primary_assembly 10: 11,086,863-11,097,034 forward strand.

GRCr8:CM070400.1

About this gene

This gene has 2 transcripts (splice variants), 193 orthologues, 17 paralogues and is associated with 6 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000061208.4	Septin12-201	1325	356aa	ENSRNOP00000057921.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6K4P8 Q4V8G5	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 P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. 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 P1,
ENSRNOT00000111695.2	Septin12-202	1268	278aa	ENSRNOP00000088547.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6A6R7 A6K4P9	-

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Summary

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