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

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Gene: Pde4c ENSRNOG00000019518

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Description

phosphodiesterase 4C [Source:RGD Symbol;Acc:727918]

Gene Synonyms

Dpde1, MGC188426

Location

Primary_assembly 16: 18,725,674-18,744,037 reverse strand.

GRCr8:CM070406.1

About this gene

This gene has 3 transcripts (splice variants), 267 orthologues and 20 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000116505.2	Pde4c-203	2108	698aa	ENSRNOP00000083315.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZZS2	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,
ENSRNOT00000113780.2	Pde4c-202	2189	631aa	ENSRNOP00000096064.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AN21	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,
ENSRNOT00000026457.8	Pde4c-201	2172	671aa	ENSRNOP00000026457.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6KA07 G3V8J8	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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