Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Strains
  - Gene tree
  - Orthologues
  - Paralogues
Ontologies
- GO: Cellular component
- GO: Biological process
- GO: Molecular function
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: 2510039O18Rikl ENSRNOG00000007968

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Description

like [Source:RGD Symbol;Acc:1305350]

Gene Synonyms

Kiaa2013, LOC313699, RGD1305350

Location

Primary_assembly 5: 163,655,106-163,661,660 forward strand.

GRCr8:CM070395.1

About this gene

This gene has 2 transcripts (splice variants) and 201 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000104148.2	2510039O18Rikl-202	3203	688aa	ENSRNOP00000079068.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZM35	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,
ENSRNOT00000010558.6	2510039O18Rikl-201	2727	634aa	ENSRNOP00000010558.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZLT7	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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