Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

Configure this page

Share this page

Bookmark this page

.

Gene: FANCI ENSGALG00010016181

.

Description

Fanconi anemia complementation group I [Source:NCBI gene (formerly Entrezgene);Acc:415491]

Location

Primary_assembly 10: 12,964,867-12,988,651 reverse strand.

bGalGal1.mat.broiler.GRCg7b:CM028491.1

About this gene

This gene has 3 transcripts (splice variants) and 200 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSGALT00010038894.1	FANCI-202	4945	1338aa	ENSGALP00010022478.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8V0YNA7	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,
ENSGALT00010038899.1	FANCI-203	4924	1331aa	ENSGALP00010022480.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8V0YUQ9	-
ENSGALT00010038885.1	FANCI-201	4803	1304aa	ENSGALP00010022474.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8V0Z1G8	-

.

Summary

.

.