Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Cellular component
- GO: Molecular function
- GO: Biological process
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: MPDU1 ENSOCUG00000010389

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Description

mannose-P-dolichol utilization defect 1 [Source:HGNC Symbol;Acc:HGNC:7207]

Location

Chromosome 19: 11,589,200-11,597,021 reverse strand.

OryCun2.0:CM000808.1

About this gene

This gene has 2 transcripts (splice variants), 252 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSOCUT00000010387.2	MPDU1-202	947	247aa	ENSOCUP00000008948.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	G1SZ66	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,
ENSOCUT00000049977.1	MPDU1-201	534	178aa	ENSOCUP00000040896.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-

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Summary

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