Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: NFX1 ENSLOCG00000011211

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Description

nuclear transcription factor, X-box binding 1 [Source:HGNC Symbol;Acc:HGNC:7803]

Location

Chromosome LG9: 32,687,778-32,727,723 reverse strand.

LepOcu1:CM001412.1

About this gene

This gene has 2 transcripts (splice variants), 213 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSLOCT00000013807.1	NFX1-201	3377	1081aa	ENSLOCP00000013778.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	W5MZG9	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,
ENSLOCT00000013816.1	NFX1-202	3416	875aa	ENSLOCP00000013787.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	W5MZH8	-

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Summary

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