Busch Lab

ZMP

WFS1 (1 of 2)

Ensembl ID:
ENSDARG00000062341
Description:
Wolfram syndrome 1 (wolframin) [Source:HGNC Symbol;Acc:12762]
Human Orthologue:
WFS1
Human Description:
Wolfram syndrome 1 (wolframin) [Source:HGNC Symbol;Acc:12762]
Mouse Orthologue:
Wfs1
Mouse Description:
Wolfram syndrome 1 homolog (human) Gene [Source:MGI Symbol;Acc:MGI:1328355]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa10021 Nonsense Available for shipment Available now
sa11465 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa10021
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000090025 Nonsense 692 1061 9 9
Genomic Location (Zv9):
Chromosome 1 (position 13199706)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 13628448
GRCz11 1 14314961
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTTCAGAGGGACGTACTGTTTCCTGGTGCCGTACTTGGTCTGCTTTGTCT[G/A]GTGYGAGTTCTCTGTGGTTCTGCTTCGGAACTCCACCACCATCGGCCTRA
Long Flanking Sequence:
CTAGTTATATACATTAGATGAAAGCCTGAAGACCTTTAATTGGGTGTTAATTGTGATTTACTGTTTAAAAGTTTTGACTGCCTCAAACAAAGTTAATGGGATTTTTTGTAGTTTCAGACATTTTATAAATAAATCTTATGTTTGATTAAAGCTTAGTTGTAGATCAGCCTAAAGCAGGGGTGTCCAAACCTGTTCCTGAAGGGCCAGTGTCCTGCAAAGTTTAGTTCCAACCCCAATCAGACACACCTTGGCAACCTAATTAAGCTCTTACTAGGCTTTCTAGAAATATAACTGGAGGTGTGTTGGGGCAAGTTGGAGCTAAAATCTGCAGAACATCGCCCTCCAGGACCAAGTTTGGATTATATATTTTGAAACTGATGTATCAATATCAAATATCATGATCAAACCTACCTCTTTTTTTGCTGTTCATAGTATGGCGCGCATGAGGGGCTTCAGAGGGACGTACTGTTTCCTGGTGCCGTACTTGGTCTGCTTTGTCT[G/A]GTGCGAGTTCTCTGTGGTTCTGCTTCGGAACTCCACCACCATCGGCCTGATCCGTACTTGTGTTGCCTACTTCCTCTTCCTGTTCGCCCTACCAGTGTTAATCATGGGTCTGATAGCTTTGCTGCTGATTCAGCTGATTAAGTGGTTCCTGGAGTTAGAGTTAACTAAGATGCTGGTGACCCTGGCAGTGTGCGCCGTCCCTGTGACACTGCGACTCTGGACTCGATTTAGCCTCTCAATTCTGAATGTCTTCCGCTCCATCACCCACCGAGGTCCAGTCAAACTGATCCTCCTGTGCATCACTACAGTGATTTTACTCTGCGGCGTCTATGTTTATAATGCTGAAGGCCTCAAGGTTTATAACTCCACACTCACCTGGGAGGAATATGGCACACTGTGCGGCCCGCAAGCCTGGAAAGAACGAGGAATGGCTCAAACGCAGCTCTCCTGCAGCCATCTGGAAGGCCATCGTGTCACATGGACAGGAATATTCCGTTATG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa11465
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000090025 Nonsense 825 1061 9 9
Genomic Location (Zv9):
Chromosome 1 (position 13199306)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 13628048
GRCz11 1 14314561
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCAAGGTTTATAACTCCACACTCACCTGGGAGGAATATGGCACACTGTG[C/A]GGCCCGCAAGCCTGGAAAGAACGAGGAATGGCTCAAACGCAGCTCTCCTG
Long Flanking Sequence:
ATCAAACCTACCTCTTTTTTTGCTGTTCATAGTATGGCGCGCATGAGGGGCTTCAGAGGGACGTACTGTTTCCTGGTGCCGTACTTGGTCTGCTTTGTCTGGTGCGAGTTCTCTGTGGTTCTGCTTCGGAACTCCACCACCATCGGCCTGATCCGTACTTGTGTTGCCTACTTCCTCTTCCTGTTCGCCCTACCAGTGTTAATCATGGGTCTGATAGCTTTGCTGCTGATTCAGCTGATTAAGTGGTTCCTGGAGTTAGAGTTAACTAAGATGCTGGTGACCCTGGCAGTGTGCGCCGTCCCTGTGACACTGCGACTCTGGACTCGATTTAGCCTCTCAATTCTGAATGTCTTCCGCTCCATCACCCACCGAGGTCCAGTCAAACTGATCCTCCTGTGCATCACTACAGTGATTTTACTCTGCGGCGTCTATGTTTATAATGCTGAAGGCCTCAAGGTTTATAACTCCACACTCACCTGGGAGGAATATGGCACACTGTG[C/A]GGCCCGCAAGCCTGGAAAGAACGAGGAATGGCTCAAACGCAGCTCTCCTGCAGCCATCTGGAAGGCCATCGTGTCACATGGACAGGAATATTCCGTTATGTTCGTGTAGCAGAGAAGGAAAATGGAGCTCAGTCTGTTATAAACATGCTACCGGTGTTCATGGGCGACTGGTTGCGGTGTCTCTACGGTGAGGTTTATCCGAAGTGTGAACCACAAAACAATTCATTTCCGATCGTGAATGTTACTCAAGTCACCACAGGAACTGTCAACACAACAATACTGATCCTAAGGCAGGAAGAGGAAGAGTTATGTCGGATAAAAGCTTATGCTACACACCAATGCCACGTTAAACGTTTTGACAGTTACCGTTTCGAGGTGACGGTTGGCATGCCGGTGGATGGTGTCACAAAAGTGGACAATCCAGCAGGTGACATTCTCTTAATGGCAAGTCATGAATTCAGACAAGTGCTGCTGAATCTTAACCCAGGCAGCATGGTGGA
Associated Phenotype:
Not determined