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

Configure this page

Share this page

Bookmark this page

.

Gene: FANCI ENSBTAG00000009097

.

Description

FA complementation group I [Source:VGNC Symbol;Acc:VGNC:28859]

Location

Primary_assembly 21: 20,722,989-20,787,646 forward strand.

ARS-UCD2.0:CM008188.2

About this gene

This gene has 2 transcripts (splice variants), 199 orthologues and is associated with 1 phenotype.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000083264.3	FANCI-201	4853	1365aa	ENSBTAP00000064713.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1N4H1	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,
ENSBTAT00000011991.7	FANCI-202	4772	1300aa	ENSBTAP00000011991.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E1BDI4	-

.

Summary

.

.