Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Biological process
- GO: Molecular function
- GO: Cellular component
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: Psg19 ENSRNOG00000038101

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Description

pregnancy specific glycoprotein 19 [Source:RGD Symbol;Acc:2334]

Gene Synonyms

CEAC, CGM3, Cea3, MGC114333

Location

Primary_assembly 1: 87,549,234-87,559,500 reverse strand.

GRCr8:CM070391.1

About this gene

This gene has 2 transcripts (splice variants), 370 orthologues and 23 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000057988.7	Psg19-202	2775	475aa	ENSRNOP00000054798.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6J8H4 G3V9P5	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 P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. 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 P1,
ENSRNOT00000057986.6	Psg19-201	2415	355aa	ENSRNOP00000054796.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q4V8L4	-

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Summary

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