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

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Gene: Fbh1 ENSRNOG00000018549

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Description

F-box DNA helicase 1 [Source:RGD Symbol;Acc:1306298]

Gene Synonyms

Fbxo18, LOC291293

Location

Primary_assembly 17: 66,749,534-66,787,590 forward strand.

mRatBN7.2:CM026990.1

About this gene

This gene has 1 transcript (splice variant), 197 orthologues and is associated with 4 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000025228.8	Fbh1-201	3530	1042aa	ENSRNOP00000025228.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1M298	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,

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Summary

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