Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
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: CERS6 ENSPTRG00000012603

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Description

ceramide synthase 6 [Source:VGNC Symbol;Acc:VGNC:131]

Location

Chromosome 2B: 58,589,995-58,909,229 forward strand.

Pan_tro_3.0:CM000316.3

About this gene

This gene has 2 transcripts (splice variants), 207 orthologues and 5 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000105396.1	CERS6-201	1629	392aa	ENSPTRP00000067582.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3RSA7 A0A6D2XHL0	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 P5: Where the APPRIS core modules are unable to choose a clear principal variant and none of the candidate variants are annotated by CCDS, APPRIS selects the longest of the candidate isoforms 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 P5,
ENSPTRT00000065769.2	CERS6-202	1349	384aa	ENSPTRP00000057335.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2XY63 K7AQD5	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,

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Summary

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