IWS1

Ensembl ID:
ENSDARG00000087950
Description:
IWS1 homolog (S. cerevisiae) [Source:HGNC Symbol;Acc:25467]
Human Orthologue:
IWS1
Human Description:
IWS1 homolog (S. cerevisiae) [Source:HGNC Symbol;Acc:25467]
Mouse Orthologue:
Iws1
Mouse Description:
IWS1 homolog (S. cerevisiae) Gene [Source:MGI Symbol;Acc:MGI:1920723]

Alleles

There is 1 allele of this gene:

Allele name Consequence Status Availability Estimate
sa22732 Essential Splice Site Mutation detected in F1 DNA During 2017

Mutation Details

Allele Name:
sa22732
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2017.
Mutation:
T > C
Consequence:
Essential Splice Site
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000125211 Essential Splice Site 688 731 17 18
Genomic Location (Zv9):
Chromosome 15 (position 45987541)
Other Location(s):
Assembly Chromosome Position
GRCz10 15 46409474
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
AGACTACGTGGTTCGGCCCAAATGGAACGTGGATGGAGATTCAAACCGGG[T/C]GAGTGGGCGGAGCTTTAGAGGAATGATTGAAAGATGTCTCTTATGCAAAT
Associated Phenotype:
Not determined

Register

If you would like to be informed when the status of this gene changes (for example, a new allele is generated or an allele is made available for distribution) then please enter your details below:

Short-link