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

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Gene: PDXDC1 ENSBTAG00000004801

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Description

pyridoxal dependent decarboxylase domain containing 1 [Source:NCBI gene (formerly Entrezgene);Acc:505868]

Location

Primary_assembly 25: 13,731,838-13,786,631 reverse strand.

ARS-UCD1.3:CM008192.2

About this gene

This gene has 3 transcripts (splice variants), 211 orthologues and 8 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000082002.2	PDXDC1-202	3821	760aa	ENSBTAP00000064477.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1M7W0	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 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,
ENSBTAT00000046463.4	PDXDC1-201	3906	709aa	ENSBTAP00000043763.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A7MBC2	-
ENSBTAT00000133840.1	PDXDC1-203	3674	695aa	ENSBTAP00000081524.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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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