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
Regulation
External references
Supporting evidence
ID History
- Gene history

Configure this page

Export data

Share this page

Bookmark this page

.

Gene: Rps12 ENSRNOG00000016411

.

Description

ribosomal protein S12 [Source:RGD Symbol;Acc:62024]

Location

Primary_assembly 1: 23,500,073-23,502,235 forward strand.

GRCr8:CM070391.1

About this gene

This gene has 3 transcripts (splice variants), 63 orthologues, 10 paralogues and is associated with 1 phenotype.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000115390.2	Rps12-202	475	148aa	ENSRNOP00000092043.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6ACY4	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,
ENSRNOT00000118437.2	Rps12-203	558	137aa	ENSRNOP00000093841.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AL68	-
ENSRNOT00000022184.6	Rps12-201	543	132aa	ENSRNOP00000022184.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F7EWX3 Q6PDW1	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,

.

Paralogues

.

.

Personal Data