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: Molecular function
- GO: Biological process
- GO: Cellular component
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: Deaf1 ENSRNOG00000017960

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Description

DEAF1 transcription factor [Source:RGD Symbol;Acc:620671]

Gene Synonyms

NUDR

Location

Primary_assembly 1: 205,831,336-205,865,106 reverse strand.

GRCr8:CM070391.1

About this gene

This gene has 2 transcripts (splice variants), 195 orthologues and is associated with 12 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000048817.5	Deaf1-201	2123	565aa	ENSRNOP00000046656.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1LQ17	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,
ENSRNOT00000094110.2	Deaf1-202	2125	535aa	ENSRNOP00000086677.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6A6A4	-

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Summary

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