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: Imp4 ENSRNOG00000013285

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Description

IMP U3 small nucleolar ribonucleoprotein 4 [Source:RGD Symbol;Acc:1308463]

Gene Synonyms

LOC316317, LRRGT00017, MGC94302, RGD1308463

Location

Primary_assembly 9: 44,150,337-44,157,751 forward strand.

GRCr8:CM070399.1

About this gene

This gene has 1 transcript (splice variant), 197 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000066913.4	Imp4-201	3963	291aa	ENSRNOP00000062237.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6INA0 Q5PQR5	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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Paralogues

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