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: 4921524L21Rikl1 ENSRNOG00000050332

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Description

RIKEN cDNA 4921524L21 gene like 1 [Source:RGD Symbol;Acc:1560860]

Gene Synonyms

4921524L21Rikl, 4921524L21Rikl2, LOC100912220, LOC103690053, LOC498767, RGD1560860

Location

Primary_assembly 17: 59,503,243-59,542,741 forward strand.

GRCr8:CM070407.1

About this gene

This gene has 1 transcript (splice variant), 6 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000077324.3	4921524L21Rikl1-201	1455	396aa	ENSRNOP00000073533.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2K5R9	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 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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