Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
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- Orthologues
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Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
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Gene: Faul1 ENSRNOG00000062652

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Description

FAU ubiquitin like and ribosomal protein S30 fusion like 1 [Source:RGD Symbol;Acc:1597505]

Gene Synonyms

LOC100360647, LOC687780

Location

Primary_assembly 1: 178,061,553-178,185,430 reverse strand.

GRCr8:CM070391.1

About this gene

This gene has 4 transcripts (splice variants), 204 orthologues and 5 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000170953.1	Faul1-204	867	157aa	ENSRNOP00000109050.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSRNOT00000170231.1	Faul1-203	1680	133aa	ENSRNOP00000100110.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000039337.7	Faul1-201	1067	133aa	ENSRNOP00000034657.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F8WGA4	-
ENSRNOT00000048726.5	Faul1-202	539	133aa	ENSRNOP00000042031.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q5BJN7	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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