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

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Gene: tmed10 ENSDARG00000041391

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Description

transmembrane p24 trafficking protein 10 [Source:NCBI gene (formerly Entrezgene);Acc:326716]

Gene Synonyms

TMP21, fe06g04, wu:fb98e10, wu:fe06g04, zgc:85681

Location

Chromosome 20: 46,536,598-46,541,843 reverse strand.

GRCz11:CM002904.2

About this gene

This gene has 2 transcripts (splice variants), 229 orthologues and 10 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000060685.4	tmed10-201	1746	209aa	ENSDARP00000060684.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q6NWI7	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 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,
ENSDART00000181720.1	tmed10-202	1748	207aa	ENSDARP00000153388.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2R8QEQ4	APPRIS P4: Where the APPRIS core modules are unable to choose a clear principal CDS and there is more than one variant with a distinct (but consecutive) CCDS identifiers, APPRIS selects the longest CCDS isoform 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 P4,

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Summary

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