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: Nfix ENSRNOG00000002983

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Description

nuclear factor I X [Source:RGD Symbol;Acc:69080]

Gene Synonyms

Nf1x

Location

Primary_assembly 19: 23,355,498-23,448,265 forward strand.

mRatBN7.2:CM026992.1

About this gene

This gene has 4 transcripts (splice variants), 279 orthologues, 3 paralogues and is associated with 11 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000091994.2	Nfix-202	1978	494aa	ENSRNOP00000071775.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2K1B6	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,
ENSRNOT00000101795.1	Nfix-203	1830	433aa	ENSRNOP00000082587.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6G7L6	-
ENSRNOT00000117437.1	Nfix-204	1466	399aa	ENSRNOP00000096564.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AV91	-
ENSRNOT00000039354.5	Nfix-201	1430	441aa	ENSRNOP00000034591.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F2Z3R4	-

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Summary

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