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: NFX1 ENSPTRG00000020858

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Description

nuclear transcription factor, X-box binding 1 [Source:VGNC Symbol;Acc:VGNC:4802]

Location

Chromosome 9: 34,021,069-34,102,143 forward strand.

Pan_tro_3.0:CM000323.3

About this gene

This gene has 2 transcripts (splice variants), 211 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000050486.3	NFX1-201	4768	1120aa	ENSPTRP00000041030.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2VZY2 H2R0P2	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,
ENSPTRT00000083550.1	NFX1-202	2502	833aa	ENSPTRP00000071352.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2XIR7 K7B8Y8	-

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Summary

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