Busch Lab

ZMP

WDR65

Ensembl ID:
ENSDARG00000058090
Description:
WD repeat domain 65 [Source:HGNC Symbol;Acc:26485]
Human Orthologue:
WDR65
Human Description:
WD repeat domain 65 [Source:HGNC Symbol;Acc:26485]
Mouse Orthologue:
Wdr65
Mouse Description:
WD repeat domain 65 Gene [Source:MGI Symbol;Acc:MGI:2686209]

Alleles

There are 5 alleles of this gene:

Allele Name Consequence Status Availability
sa16621 Essential Splice Site Available for shipment Available now
sa10548 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa16621
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:
A > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000080900 Essential Splice Site 721 1054 13 17
Genomic Location (Zv9):
Chromosome 2 (position 13397867)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 13922849
GRCz11 2 13605635
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCCTAKTTCAATAGAGAAATTATTTTGTAATAATTTTATTTTTTATTGC[A/C]GGTACTGAAAAAAGAGAAAGACAACCAACAAGAAGCCCACAATAAAGCTA
Long Flanking Sequence:
TTTTTTTTTTTGCATTATTTTTGAAATTACTTTGTATTACATAAATAGAGATATTTGGTTGGAGTTCATTTACCTACTCCCTCTCAGCATCTGGTACTACTCTGGTTGGAATGGAAATGTGATTTTGCAGGAGAAAGTTGAAACACCCCTATTGATCCCAAAAATTGTTAAATAATCAAAAAAAAAAAAAAAAAAAGTGAAATATAAGATTCTATTTTACCCTGTTGCATAATTACAGCCTTTTCTCATATCATTTTGAACAGAGTAAAATGCTGCTTGAACTGAATGCAAAAGTAGAAGAGCTCCAGGAAGACAACAAGTGCCAGCTAAGCTTGAAAGATACTGAATACAATAAGAAGATCAATGAGCTATCTGAAAAGTGTATGCAACAGATAATTTCACTAAATGCCGAGAAGGAGGTGAGTTTAAAGAAACCCATAATGAAAAACATTCCTATTTCAATAGAGAAATTATTTTGTAATAATTTTATTTTTTATTGC[A/C]GGTACTGAAAAAAGAGAAAGACAACCAACAAGAAGCCCACAATAAAGCTATATCAGACATCTTAGAGAGACATGATAAAGAGCTTCACGACATGGGTAAAAAAAAAGTTTCATTTATTTTATTTAAATGAATTTCTAAAAAGACACTTCACTACTCGATTGTTAAAGACAGAGACTTTTACAAGCTTTGAGGTCTTGCTATTTTGTCTAAAAAGTGACAATAACTTCTTGATTGTGGTTATATATCGTCCTCCTAAGTTTAAAAAAAATAATTTATTCATTGAATTGTATGACTTTCTTGGCAGACTTGTTTCTCAATTTGATAAGCTTCTAATGGTGGAATATAATATTTTAATGTTCATGTTTGTTGTGATGCAAACCCCCTCACTAAGGAGTTTTTAAGTCTTATTGTCACCTACGAGATATCCCAAACGGTTACAGGTCCTACACATTAATTTGGTCATACCTTGGATCTTGTTCTGTCATATGGTTTCATGATTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10548
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000080900 Nonsense 851 1054 15 17
Genomic Location (Zv9):
Chromosome 2 (position 13460042)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 13985024
GRCz11 2 13668262
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGAGGAGGACACAGATGCTGAAATTCATGACATCCGCATGAAATATGAG[C/T]AAAATCTAAGAGAAGAAAAAAAGGCCCATTCAAAGCTCAAAGTGGAATTG
Long Flanking Sequence:
CAGTAATTTTGAGCTTTAGTATTGCGGTACAGGGAACTACAGGGAAGGCAACAGGGTAGTATATCTACAGGGAGTGGTACAGCTCCCTGTTGTGCTGCCCCACCACCCAGAGATATGCAGAGATAAATGGGGCCAAACATCTGTTTTAGTTGGCTCCCAATTGATGATCTTGGCAACAGCTGGTCCATCTGCAATCCCAGGGTTGTTAAAGAAATTACTGTCTCAAAGACTTGTGCTCTCTTTTATTCAAGCTATTTGGTGATGTTAATAGATTTTTTTGGATCTTGGGATCAAAAATATTATGATATTAGGCCTTTTGTTAGGCCAAATTGTCATGTGCAGGACTGTGTTATCATTTGCAAACATAACAATTTTTCACTCTTTACTTTTTGCAGTATCAAGATGAATCCCAGCAGCGGTTTAAAGAATTTGAAGAACACATAAGGCAGGAAGAGGAGGACACAGATGCTGAAATTCATGACATCCGCATGAAATATGAG[C/T]AAAATCTAAGAGAAGAAAAAAAGGCCCATTCAAAGCTCAAAGTGGAATTGGATACCACAAAAAAACGGGTAAGTGACTATTTGTGCATTCCAAGCAAGATGTAATGCCCTCTAAAGGGCCCTTTACCGTGAAAAAAAAAATCATGGCCATCATATTACAGTGTAATTCCAAATTGAAGTTAAGGCCCTTTGCAATGTAGGAATCTGAAAAATACAACTGATGGCAACTTCAGGACAATGTCCTTTGAGCAGGGAAGCTTTTTGGTGTCACACACTGCACTTAATTCAGAAGGGCTCACTAACATGAGCAAACTATGAACAACACATTTACTACAGTATTTAATGTTTGCTAATGTTAATGAAAATGCAGTTGTTCACAATTACTCTCAGTGCATTAACTAATGTTAATGTAATTGAACTGAACTATGTAATTGAACTGTCTTTAATAAATGCTTCAGAAGAATTGTGCATTATTAGTTGGTGAATGCAATAACTAAAATT
Associated Phenotype:
Not determined