Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Strains
  - Gene tree
  - Orthologues
  - Paralogues
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

Configure this page

Export data

Share this page

Bookmark this page

.

Gene: Srp19 ENSRNOG00000020204

.

Description

signal recognition particle 19 [Source:RGD Symbol;Acc:1308437]

Gene Synonyms

LOC291685

Location

Primary_assembly 18: 26,205,796-26,226,635 forward strand.

GRCr8:CM070408.1

About this gene

This gene has 3 transcripts (splice variants), 218 orthologues and is associated with 4 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000097724.2	Srp19-202	1513	144aa	ENSRNOP00000091385.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AFH8 B2RZ66	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,
ENSRNOT00000027418.9	Srp19-201	977	139aa	ENSRNOP00000027418.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F7F3N8	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,
ENSRNOT00000108712.2	Srp19-203	822	120aa	ENSRNOP00000077002.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5Y7C0 A6J2U0	-

.

Gene tree

.

.