Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
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Comparative Genomics
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- GO: Cellular component
- GO: Molecular function
- GO: Biological process
Phenotypes
Genetic Variation
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ID History
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Gene: Tmem222 ENSRNOG00000008564

Description

transmembrane protein 222 [Source:RGD Symbol;Acc:1304793]

Gene Synonyms

LOC313021, RGD1304793

Location

GRCr8:CM070395.1

About this gene

This gene has 2 transcripts (splice variants), 262 orthologues and is associated with 2 phenotypes.

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000115126.2	Tmem222-202	1767	262aa	ENSRNOP00000094132.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AIW6	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 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,
ENSRNOT00000011357.7	Tmem222-201	1400	206aa	ENSRNOP00000011357.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F7FIL2	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,

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