Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: nfixa ENSDARG00000043226

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Description

nuclear factor I X [Source:HGNC Symbol;Acc:HGNC:7788]

Location

Chromosome 1: 51,896,147-52,086,496 forward strand.

GRCz11:CM002885.2

About this gene

This gene has 2 transcripts (splice variants), 212 orthologues, 3 paralogues and is associated with 10 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	Flags
ENSDART00000167139.2	nfixa-202	1299	432aa	ENSDARP00000137992.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	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,
ENSDART00000135861.3	nfixa-201	1764	204aa	ENSDARP00000112653.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-

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Summary

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