Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Molecular function
- GO: Biological process
- 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: Rnf122 ENSRNOG00000023473

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Description

ring finger protein 122 [Source:RGD Symbol;Acc:1561238]

Gene Synonyms

LOC502091, RGD1561238

Location

Primary_assembly 16: 67,712,936-67,730,479 reverse strand.

GRCr8:CM070406.1

About this gene

This gene has 2 transcripts (splice variants), 235 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000116029.2	Rnf122-202	1514	183aa	ENSRNOP00000088658.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AJB0	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,
ENSRNOT00000031701.8	Rnf122-201	1744	155aa	ENSRNOP00000037851.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1LZF5	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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