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
External references
Supporting evidence
ID History
- Gene history

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Gene: LOC120102832 ENSRNOG00000055292

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Description

RNA-binding protein 12B-A-like [Source:RGD Symbol;Acc:41100894]

Gene Synonyms

LOC313069, RGD1307658

Location

Primary_assembly 5: 30,385,003-30,404,090 forward strand.

GRCr8:CM070395.1

About this gene

This gene has 5 transcripts (splice variants), 276 orthologues and 9 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000163290.1	LOC120102832-204	13323	843aa	ENSRNOP00000108366.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSRNOT00000128493.1	LOC120102832-203	11467	843aa	ENSRNOP00000106384.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000122529.1	LOC120102832-202	11009	843aa	ENSRNOP00000107293.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000173684.1	LOC120102832-205	10223	843aa	ENSRNOP00000103713.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000115566.2	LOC120102832-201	7998	843aa	ENSRNOP00000089816.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6ADB2	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,

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Summary

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