Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Strains
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  - Orthologues
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Ontologies
Phenotypes
Genetic Variation
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- Structural variants
Gene expression
Pathway
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Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: Impact ENSRNOG00000045844

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Description

impact RWD domain protein [Source:RGD Symbol;Acc:1591977]

Location

Primary_assembly 18: 4,108,853-4,147,569 forward strand.

mRatBN7.2:CM026991.1

About this gene

This gene has 2 transcripts (splice variants), 209 orthologues and is associated with 2 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000116602.1	Impact-202	3543	317aa	ENSRNOP00000078372.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q5GFD9	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,
ENSRNOT00000073771.3	Impact-201	3212	297aa	ENSRNOP00000064200.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2QV96	-

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Summary

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