Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
Ontologies
- GO: Cellular component
- GO: Biological process
- GO: Molecular function
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: IMPACT ENSCAFG00845013207

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Description

impact RWD domain protein [Source:HGNC Symbol;Acc:HGNC:20387]

Location

Primary_assembly 7: 64,005,895-64,035,299 reverse strand.

ROS_Cfam_1.0:CM025106.1

About this gene

This gene has 2 transcripts (splice variants) and 209 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSCAFT00845023564.1	IMPACT-202	1048	330aa	ENSCAFP00845018500.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8C0P7Z4 A0A8I3NPE0	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,
ENSCAFT00845023520.1	IMPACT-201	3580	319aa	ENSCAFP00845018461.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I3NF59	-

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Summary

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