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

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Gene: nfic ENSDARG00000043210

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Description

nuclear factor I/C [Source:ZFIN;Acc:ZDB-GENE-080305-2]

Location

Chromosome 8: 20,624,510-20,795,631 forward strand.

GRCz11:CM002892.2

About this gene

This gene has 3 transcripts (splice variants), 74 orthologues and 3 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000088668.7	nfic-201	1563	520aa	ENSDARP00000083101.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1QBH7	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,
ENSDART00000138604.3	nfic-203	1725	499aa	ENSDARP00000118559.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	B0S4Z1	3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete,
ENSDART00000135850.2	nfic-202	435	145aa	ENSDARP00000114279.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1QF29	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, 5' and 3' truncations in transcript evidence prevent annotation of the start and the end of the CDS.CDS 5' and 3' incomplete,

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Summary

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