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: Ubc ENSRNOG00000057823

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Description

ubiquitin C [Source:RGD Symbol;Acc:621244]

Location

Primary_assembly 12: 36,900,127-36,905,275 forward strand.

GRCr8:CM070402.1

About this gene

This gene has 4 transcripts (splice variants), 62 orthologues and 22 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000166204.1	Ubc-204	3416	962aa	ENSRNOP00000107356.1	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,
ENSRNOT00000102498.2	Ubc-202	2699	773aa	ENSRNOP00000078230.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1LML2	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,
ENSRNOT00000102889.2	Ubc-203	2620	646aa	ENSRNOP00000080954.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZR71	-
ENSRNOT00000085692.3	Ubc-201	2344	734aa	ENSRNOP00000074688.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1LML2	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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