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
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: nfixb ENSLACG00000016266

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Description

nuclear factor I/Xb [Source:ZFIN;Acc:ZDB-GENE-060421-5000]

Location

Scaffold JH126758.1: 1,509,139-1,510,533 forward strand.

About this gene

This gene has 2 transcripts (splice variants), 99 orthologues and 5 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSLACT00000018605.1	nfixb-201	612	203aa	ENSLACP00000018472.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	H3B9A1	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,
ENSLACT00000018606.1	nfixb-202	582	193aa	ENSLACP00000018473.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	H3B9A2	-

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Summary

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