Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
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: Tmem9 ENSRNOG00000010204

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Description

transmembrane protein 9 [Source:RGD Symbol;Acc:1307922]

Gene Synonyms

LOC289046

Location

Primary_assembly 13: 50,010,250-50,027,553 forward strand.

GRCr8:CM070403.1

About this gene

This gene has 1 transcript (splice variant), 207 orthologues, 1 paralogue and is associated with 4 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000013738.8	Tmem9-201	1594	183aa	ENSRNOP00000013738.8	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2JUD1 A0A8J8YFY6 A6ICH5	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,

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Summary

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