Summary
- Splice variants
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- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
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Gene: Wfs1 ENSRNOG00000005108

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Description

wolframin ER transmembrane glycoprotein [Source:RGD Symbol;Acc:68954]

Location

Primary_assembly 14: 73,810,404-73,835,602 forward strand.

mRatBN7.2:CM026987.1

About this gene

This gene has 2 transcripts (splice variants), 268 orthologues and is associated with 40 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000034730.5	Wfs1-201	3208	890aa	ENSRNOP00000032218.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E9PT53	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 P5: Where the APPRIS core modules are unable to choose a clear principal variant and none of the candidate variants are annotated by CCDS, APPRIS selects the longest of the candidate isoforms as the principal variant. 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 P5,
ENSRNOT00000109032.1	Wfs1-202	3038	858aa	ENSRNOP00000087329.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6A452	APPRIS ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2,

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Strains

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Genomic alignments

Gene tree

Orthologues

Paralogues (Not available)

Families (Not available)

More views of comparative genomics data, such as multiple alignments and synteny, are available on the Location page for this gene.

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