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: Molecular function
- GO: Biological process
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: RGD1561916 ENSRNOG00000013320

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Description

similar to testes development-related NYD-SP22 isoform 1 [Source:RGD Symbol;Acc:1561916]

Gene Synonyms

LOC500441

Location

Primary_assembly 5: 56,666,058-56,678,923 reverse strand.

mRatBN7.2:CM026978.1

About this gene

This gene has 2 transcripts (splice variants) and 108 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000017903.9	RGD1561916-201	1145	297aa	ENSRNOP00000017903.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D4A9U1	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,
ENSRNOT00000112029.1	RGD1561916-202	995	231aa	ENSRNOP00000085022.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZZ70	-

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Summary

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