ZMP
WDR65
Ensembl ID:
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 |
---|---|---|---|
sa38319 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa8390 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa16621 | Essential Splice Site | Available for shipment | Available now |
sa10548 | Nonsense | Available for shipment | Available now |
sa19696 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa38319
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000080900 | Nonsense | 119 | 1054 | 2 | 17 |
Genomic Location (Zv9):
Chromosome 2 (position 13258223)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 13783448 |
GRCz11 | 2 | 13466234 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGGTGGTGGATGAGTTTGTCTGCATGGCCTTTTCTCCTGACTCAAAGTA[T/G]CTGATTGGTCAGGCAGGTGGGCCAGACTGGACTCTTTTTCTCTGGATGTG
Long Flanking Sequence:
TCCATGAAGGATTAAGGCAGTTCTGAAGACAAAAGGGGGTAAAATCTGGTACTAGTAAGGGGTACCTAATAAAGTGGCCAGGGAGTGTATTTCTCGTCTAATGCAGAAAATGTTTATATGATATGAAAATACCATAGAAGGCAAATAGCAGATTTTAAATACACAAATTAATAAACACTGCAAATTATGTTTATGCAAACTATGTTTGAGATAAAATGTGACCTGGCCTCACATATTTTAGATCATCTGATTGCTGTATTTAACTCTATGGTAACCAGCATTTGTTTCCTGATCACAGGTACAGAGAGAAGTCAGGGCATGCATGCTTTGGCCATCAGCACAAACAGGCGCTATCTGGCTGTGTCTGAATGTAGAGAGAAAGCCACCATCACTGTGTTTGATTTAGAGCAAGAGCAGAACAGAAGGAGGAAAGTGTTGACCGGAGGAGAGATGGTGGTGGATGAGTTTGTCTGCATGGCCTTTTCTCCTGACTCAAAGTA[T/G]CTGATTGGTCAGGCAGGTGGGCCAGACTGGACTCTTTTTCTCTGGATGTGGGAAAAGAAGAAGGTCATGGCTACTGTAAATATTAGCAACAATGGGCCCATCAACCAGGTAAATATGCTTATAAAAAAGTAGGGCTTGAAATTGGCATTCTTTTTAATTTCTATCATTTTAGACGGGGTCGGGCCGGGCTTTACTTGGGCAGTAAATGAACAGTTATGTGATGCATTTCGATTAGTGCGAGAAAGTAATTAAATGTTTCAAAGGTGAAACAAAAGATGACTGAGAAGTCAAAAAGAACGACTTTTGACTGTGGTCAGGCCAGCCACCAGTTCAGAAAGAACCTATCATTCTAGCTGCAAAGGTCTTTCAGCGGTCACTCATACACTGGGTATTAAGTAAGATCGCTAAACAGCACAGCAAGCTGACAGGGAAGATGATGAGGCCACTCGCTACATTGTAACTGCTGTCATGAAAAATTAAATGGACGTTCTTGGTTGGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8390
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000080900 | Nonsense | 262 | 1054 | 4 | 17 |
Genomic Location (Zv9):
Chromosome 2 (position 13290835)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 13816060 |
GRCz11 | 2 | 13498846 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCAGATGAACCCTTCTCTGCGCTGCCACAGGTTACAGYCATCGTAAGTTA[T/A]TCTAATGGATTWGCTTGCTCCATGGGTCAAGGAACTGTGTGTTTGTTTGA
Long Flanking Sequence:
GACACCCTTAACGGGTATCATTTAATGCTGAATAAAGCATGTAATCAGTACCTGAAGTGATCATTGTCATAGTTTATGCTGTTATTTCAGCTGCAATGCCACGGTAAGAAACAGTTTCACAAAAAGAAATTTCAGGTGTTGCAGATGGTTAGGACAAAATCTCCTTTTAACATTTAACAAAATATTCCTTTTATCACATGTAGTCATGTGTTGTTAGGAAACAGTGTATGCTCGATAGTCAAACATGCTCCTGTTGGTGTCGACAATCGGACAAATTACATGGAGTCGAGCCAGGTGGAAAAACCTATTTCAGTGTTTTAAATTTGCACTGTCAATCCTACAGTATATTCTGCACTTTTGACATATCAAGTTTTCTGAATGAGAATTGCTTTCATTGTTGTATCTTCCCTGCGCTTCATTTTATCTTGCAGTGAGTCAAAACAGCAGTATTCAGATGAACCCTTCTCTGCGCTGCCACAGGTTACAGCCATCGTAAGTTA[T/A]TCTAATGGATTTGCTTGCTCCATGGGTCAAGGAACTGTGTGTTTGTTTGAGAAAACCGAGAAGGCAGATCTCTACAAGAAGACCAGAGTCATAAAGGTGCCATGACATTGTAATGTTTTTGTTTTAGTATTAAAAACTTTATTGAAATTTTTTAACTGTTTTTTTTTTTTTTTTTTTTTTTTTTCAGATTCCTCCAAAACGTTTTAGTAACGATCTCAGTTTAACAGAGAAGCAGAAAATCAGCACTCTCTGCATCAGTCCATCAGAAGAGACTCTGGTTGCCAGCACAGACCTTGGACAGCTCTACAGCATCCATCTCTCCATAGCTGAGTTACAAAAGGTGCAGTCTGCCCAACTGTTGTAGACTAATGTCATTTTGTATTTTTAGAATTTTTCGGGTTTTTTTTTTATTTTAATTTATTAAATATTTTGTACTGATTGAAATGAAATTTAATTATTCTGTGTTCTTGTTATCTACTGTACTTGTATGTATAGAGGCT
Associated Phenotype:
Not determined
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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
Mutation Details
Allele Name:
sa19696
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000080900 | Nonsense | 977 | 1054 | 17 | 17 |
Genomic Location (Zv9):
Chromosome 2 (position 13461331)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 13986313 |
GRCz11 | 2 | 13669551 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAGAAAATGAAATCCAACAGCAAAAGGACCAGATGGTGGAGGTAGGATG[C/A]ATTTTAACTCCCTGGGATTGGCAAACGCATAAATGCGTTTTAGTACATAA
Long Flanking Sequence:
CACTCTTATTGTATCTATTAATATTTTAGCTTATTAAATATTTTTTACATTATATTACATTTGATATTCTAGCCTTAGTCTTAACTAAAATATAATTTAATTCTAGTGATATTTATGTTTTTTATATATTCTAGATTTAGTTGAAGAAAATATAACCAGTTCATTTAAATCACAATATGTACATTTTACTTATCTAAAAAAATTCTAAGCTCATTGTATACGACTGGAGAACACACAAAACATGAGTGATACTAAAATAATTAAGCAACATGGATTCAGTCCATGTGAGTATGACTAGTTTCAGCGAAGGAACAGTACTTGAGAGAAACATCTGCTCTGTCTCAACAGGAAAAAAACATCTTTCAGTTAAAAAAGAAGAATGACACACTGAACAAAACACTTGAAGTGATGGAGTTCAGGGCTGAATATATGCAGGAGCAGATTGAGCCGAAAGAAAATGAAATCCAACAGCAAAAGGACCAGATGGTGGAGGTAGGATG[C/A]ATTTTAACTCCCTGGGATTGGCAAACGCATAAATGCGTTTTAGTACATAATGCACAAAAGGACCTTGAAAATGTTTTAATTGCATTAATAAGACAAACACAGATTGCAAAACTGCAAAGGGTCTATTTCTATTTGTATCTATTACTAATTACAATAAAACAATGTGTTTGTAAATCACAATTTGTAAATCAGACAGAGAGAGTGCCTTATCTTTCTGTGTCTTCTGTTAACTGAACTGGCAAACATATCAAAGAAAACAGCTAAATCTCTGTTAACGTTTGCCTCACAGACCTGTGAGACATACCTGAATAAAGCCTGAAGTGTGTAATCAAATATAATGTATTTTTGGGAACAGTTCCTGGCTCTGGCTTACCTAATTTATACAGCCTAACAATTCTTTAGAGTATTTTGATTTCAAAAGCAGTGTTGTTTTATGAACTCTAAAAAAACACAGGTTAAAAAATTACCCAAATTGGGTTGTTTTTAACCGTACTGCTGAG
Associated Phenotype:
Not determined