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

Gene: Proser3 ENSRNOG00000024625

Description

proline and serine rich 3 [Source:RGD Symbol;Acc:1565712]

Gene Synonyms

LOC361541, MGC188051, RGD1565712

Location

GRCr8:CM070391.1

About this gene

This gene has 2 transcripts (splice variants) and 117 orthologues.

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000032363.6	Proser3-201	3742	708aa	ENSRNOP00000032379.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F7ELW7	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,
ENSRNOT00000144036.1	Proser3-202	3601	698aa	ENSRNOP00000108765.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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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