Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Strains
  - Gene tree
  - Orthologues
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Ontologies
Phenotypes
Genetic Variation
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Gene expression
Pathway
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Regulation
External references
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ID History
- Gene history

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Gene: Fanci ENSRNOG00000016689

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Description

FA complementation group I [Source:RGD Symbol;Acc:2321863]

Gene Synonyms

LOC100360594

Location

Primary_assembly 1: 133,327,297-133,383,640 forward strand.

mRatBN7.2:CM026974.1

About this gene

This gene has 2 transcripts (splice variants), 200 orthologues and is associated with 26 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000050759.7	Fanci-201	4383	1332aa	ENSRNOP00000043744.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3Z840	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,
ENSRNOT00000110421.1	Fanci-202	4228	1213aa	ENSRNOP00000095393.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6ANG0	-

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Summary

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