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

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Gene: FAN1 ENSPTRG00000006854

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Description

FANCD2 and FANCI associated nuclease 1 [Source:VGNC Symbol;Acc:VGNC:14639]

Location

Chromosome 15: 11,139,863-11,179,285 forward strand.

Pan_tro_3.0:CM000329.3

About this gene

This gene has 2 transcripts (splice variants) and 200 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000012654.5	FAN1-201	4889	1017aa	ENSPTRP00000011713.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	H2Q925	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,
ENSPTRT00000108459.1	FAN1-202	1296	431aa	ENSPTRP00000069418.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3RXH9	-

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Summary

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