ZMP
LOC100333062
Ensembl ID:
Human Orthologue:
WDR81
Human Description:
WD repeat domain 81 [Source:HGNC Symbol;Acc:26600]
Mouse Orthologue:
Wdr81
Mouse Description:
WD repeat domain 81 Gene [Source:MGI Symbol;Acc:MGI:2681828]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa39050 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa22655 | Nonsense | Available for shipment | Available now |
sa35894 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa22654 | Nonsense | Available for shipment | Available now |
sa22653 | Nonsense | Available for shipment | Available now |
sa14473 | Essential Splice Site | Available for shipment | Available now |
sa11031 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa39050
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 |
---|---|---|---|---|---|
ENSDART00000111927 | Nonsense | 40 | 2065 | 1 | 11 |
Genomic Location (Zv9):
Chromosome 15 (position 25904501)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 26635284 |
GRCz11 | 15 | 26568160 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCGACCCAATGAGTTGGTGGTCCTGGTTCCAACCCGCTGGGTAATGGCCT[T/A]GAGAAACAAGAGAGTTACTCGCTGTGCAAAATATGAGAGCTTCAGTGAGG
Long Flanking Sequence:
GGCCTTGAGTTGGATTTAAAAAAAAATGTAAAACTGCTTTTGTTGTAGCCAAAATAAAATAAATAAGACTTTTTTTCAGAAGAAAAAAATTATAGGAAATTCTGTGAAAAATTTTTTGCTCTGTTAAACAATAATTTTGACTACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACATATATACATACACATATACATACACACACCACACACACACACAGATATATATATATATATATATATATATAGTGTTTTTCAGTTTACTTCCATTTACATTCCATTTCTGACATTTTCTTAGCTTCTTATAGGAGCCCACAAGTGCCACATTCTGATTGACTGAGATACATCATGGAGTGGCTAGCACCAGCCTTGGAGAGGGACCTGGGTATTGATCAGCGGCAGACTGCACATAGTCAGCGACCCAATGAGTTGGTGGTCCTGGTTCCAACCCGCTGGGTAATGGCCT[T/A]GAGAAACAAGAGAGTTACTCGCTGTGCAAAATATGAGAGCTTCAGTGAGGGGGAAATCTGCACACTTCTCCAGCGCTCTCAAATGAAACTGCCATCTGGCTGGACACGTGTTTGCATCCAAGGTCTTCGAAAGCGTAAACTCGGATACCGTTTCGCCAGGGAAACTGGCTGCCATGGGGAGGGACTCTCCCAGGACTCTTTCATGACTCTCATGCAGGGAGTATCACAGTCTAATTTCAGGTACAATGCTTTCTGTTTACTAAATGCTTTTGTTTACATTTGCTTAAATTTGTTTTTATACAGTTAACTAAAAAGTCTGTATTCATATGTGTTATACAATATATGTAAAGCATTTTTACTGATGGATACATTTATTGCGCATTCTCATTTCTCTTATGTTTACATTTAGATGACTTTTAGTTCACTATAAAAGTCATTAATTATAGACTGTTCACACTTTTAAATGTAATTTCAGCAAATTTCAAAATTCTTGATTTATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22655
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 |
---|---|---|---|---|---|
ENSDART00000111927 | Nonsense | 83 | 2065 | 1 | 11 |
Genomic Location (Zv9):
Chromosome 15 (position 25904373)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 26635156 |
GRCz11 | 15 | 26568032 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCAAATGAAACTGCCATCTGGCTGGACACGTGTTTGCATCCAAGGTCTT[C/T]GAAAGCGTAAACTCGGATACCGTTTCGCCAGGGAAACTGGCTGCCATGGG
Long Flanking Sequence:
CAATAATTTTGACTACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACATATATACATACACATATACATACACACACCACACACACACACAGATATATATATATATATATATATATATAGTGTTTTTCAGTTTACTTCCATTTACATTCCATTTCTGACATTTTCTTAGCTTCTTATAGGAGCCCACAAGTGCCACATTCTGATTGACTGAGATACATCATGGAGTGGCTAGCACCAGCCTTGGAGAGGGACCTGGGTATTGATCAGCGGCAGACTGCACATAGTCAGCGACCCAATGAGTTGGTGGTCCTGGTTCCAACCCGCTGGGTAATGGCCTTGAGAAACAAGAGAGTTACTCGCTGTGCAAAATATGAGAGCTTCAGTGAGGGGGAAATCTGCACACTTCTCCAGCGCTCTCAAATGAAACTGCCATCTGGCTGGACACGTGTTTGCATCCAAGGTCTT[C/T]GAAAGCGTAAACTCGGATACCGTTTCGCCAGGGAAACTGGCTGCCATGGGGAGGGACTCTCCCAGGACTCTTTCATGACTCTCATGCAGGGAGTATCACAGTCTAATTTCAGGTACAATGCTTTCTGTTTACTAAATGCTTTTGTTTACATTTGCTTAAATTTGTTTTTATACAGTTAACTAAAAAGTCTGTATTCATATGTGTTATACAATATATGTAAAGCATTTTTACTGATGGATACATTTATTGCGCATTCTCATTTCTCTTATGTTTACATTTAGATGACTTTTAGTTCACTATAAAAGTCATTAATTATAGACTGTTCACACTTTTAAATGTAATTTCAGCAAATTTCAAAATTCTTGATTTATTATGTGCATTAAAATTTGATTATTATTATCATTATTATTATTATTATTTAAGCAAAATAAACTCAAATTCTTCTCTACCTATATATTATTTTCTAAGCATCTGTGAATCAGTGTGTACTTGTAATATCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35894
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:
A > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111927 | Essential Splice Site | 120 | 2065 | 2 | 11 |
Genomic Location (Zv9):
Chromosome 15 (position 25903814)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 26634597 |
GRCz11 | 15 | 26567473 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGACTATTAATAAATAAATTTAATTATTTATTTATTTGTTTGTATTCCC[A/C]GAAATCTGTGGCATGAAGCGTACATGACTCATGTGCAGCCATATGCAGAT
Long Flanking Sequence:
CTCCCAGGACTCTTTCATGACTCTCATGCAGGGAGTATCACAGTCTAATTTCAGGTACAATGCTTTCTGTTTACTAAATGCTTTTGTTTACATTTGCTTAAATTTGTTTTTATACAGTTAACTAAAAAGTCTGTATTCATATGTGTTATACAATATATGTAAAGCATTTTTACTGATGGATACATTTATTGCGCATTCTCATTTCTCTTATGTTTACATTTAGATGACTTTTAGTTCACTATAAAAGTCATTAATTATAGACTGTTCACACTTTTAAATGTAATTTCAGCAAATTTCAAAATTCTTGATTTATTATGTGCATTAAAATTTGATTATTATTATCATTATTATTATTATTATTTAAGCAAAATAAACTCAAATTCTTCTCTACCTATATATTATTTTCTAAGCATCTGTGAATCAGTGTGTACTTGTAATATCTTTCTTATAGTGACTATTAATAAATAAATTTAATTATTTATTTATTTGTTTGTATTCCC[A/C]GAAATCTGTGGCATGAAGCGTACATGACTCATGTGCAGCCATATGCAGATTCCGTTGAGCAGACACCTGTTTTGGCCTTAGATGCTGTTCGTCAAGCCCTGCAGAAACTGTTTTGCTCCAACTTTATCTCTACTGATCGAGTGTCGCCATCCCTATCTCCAGCTAAAGAGAAAGAAAAAGACTGCCCATTCCTATCCACCTGCTCAGCTCCCAAACAAAGTACAGAGAGTTTATGTCCTAATGTGCTACCCGCAGAATGCTTGTTGGAGTCGGAGGAGGTCCTTTATGTGGTTTTCCCATACACACAATACACTGTTCATGATATCGTCACTTACAGTCCAGCTAAGCTTGCTAACAGCAATGCGAAAATATTGTTCATTTTGTACCAGTTACTAATTGCAATGCGGGAATGTCATGCCTCAGGGCTGTTGTGTGGTGAACTCTCCTTACTTGATATTGCAGTTGATGAGCAGCTCTGTAGTCGCCTAAAGATCTCACTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22654
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 |
---|---|---|---|---|---|
ENSDART00000111927 | Nonsense | 277 | 2065 | 2 | 11 |
Genomic Location (Zv9):
Chromosome 15 (position 25903343)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 26634126 |
GRCz11 | 15 | 26567002 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGGGCTGTTGTGTGGTGAACTCTCCTTACTTGATATTGCAGTTGATGAG[C/T]AGCTCTGTAGTCGCCTAAAGATCTCACTTGCACACTATGAAAAGTTTAAG
Long Flanking Sequence:
TAATTATTTATTTATTTGTTTGTATTCCCAGAAATCTGTGGCATGAAGCGTACATGACTCATGTGCAGCCATATGCAGATTCCGTTGAGCAGACACCTGTTTTGGCCTTAGATGCTGTTCGTCAAGCCCTGCAGAAACTGTTTTGCTCCAACTTTATCTCTACTGATCGAGTGTCGCCATCCCTATCTCCAGCTAAAGAGAAAGAAAAAGACTGCCCATTCCTATCCACCTGCTCAGCTCCCAAACAAAGTACAGAGAGTTTATGTCCTAATGTGCTACCCGCAGAATGCTTGTTGGAGTCGGAGGAGGTCCTTTATGTGGTTTTCCCATACACACAATACACTGTTCATGATATCGTCACTTACAGTCCAGCTAAGCTTGCTAACAGCAATGCGAAAATATTGTTCATTTTGTACCAGTTACTAATTGCAATGCGGGAATGTCATGCCTCAGGGCTGTTGTGTGGTGAACTCTCCTTACTTGATATTGCAGTTGATGAG[C/T]AGCTCTGTAGTCGCCTAAAGATCTCACTTGCACACTATGAAAAGTTTAAGGAGTATAGGGATGCTGTTCCATATGCTTTACAAAATAAAGTGCCAATGAGTGTTTCAACAAAGGACAATCACAATAATGGTGTGAGTGGACAGCTTTGTCGAAATTGTCAGGATGAACTTAAATCTCTGGTCCTAGACTGGGTCAACGGTCAGGTCAGCAACTTCCAGTATCTGATGGAGTTAAATCGACTAGCTGGGAGGCGTGAAGGAGACCCAAACTATCACCCTGTTTTACCTTGGGTGGTTGATTTTACTGTGCCATATGGAAGGTTTCGTGATCTTAAGAAGTCAAAATTTCGTCTAAATAAGGGTGATAAACAACTTGACTTCACGTACGAAATGACCAAAGAAGCACTGGCAGCAGTTAGCGGAAGTGGTGGAAGTAATTATCCTCCAGATCTTGGTGGACCAGTGGTACCTGGTGGTCCAGGCCAGTCGGATCACCTTCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22653
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111927 | Nonsense | 1516 | 2065 | 7 | 11 |
Genomic Location (Zv9):
Chromosome 15 (position 25898340)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 26629123 |
GRCz11 | 15 | 26561999 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTAACAACATTATTTAATAATATTAAATCCTTTTCTTTTGGTGCAGATT[G/T]GAAGTGCCCCACGTAGGGAGGTTGCAGAGTGCACATACCTGGACTTGCGC
Long Flanking Sequence:
ATTCAATAATTTTTCTTTAGTTCCTTTATTAATCTGGGGTCACCACAGTGGAATGAACCGCCAACTTATCCAGCATTTGTTTTATGCAGCGGATGCCCTTCCAGCTGCAACCCATCACTGGGAAATATCTATACACACTCAGTCACACACATACGTTATGGACAATTTAGCTCACCCAATTCACCTATATCGCATGGCTTTGGACTGTGGGGGAAACCGGAGCACCCGGAGGAAACTCATGCGAACTCGGGGAGAACATGCAAACTCCATACAGAAATGCCAACTGACCTAGTCGAGGCTTGAACCAGTGACCTTCTTGCTGTAAGGCGATTGTGCTACTCTCTGTGCCATCGTGATGCCTGTTTGATTTCATATCAACCTTAAATATTGGCTTATTTTAAAAGAATCCTCAGAGAATTGTTAATATTTAGCTGATGCAGTTTGAGATCCTTTAACAACATTATTTAATAATATTAAATCCTTTTCTTTTGGTGCAGATT[G/T]GAAGTGCCCCACGTAGGGAGGTTGCAGAGTGCACATACCTGGACTTGCGCATTCCAGATGGAGCAGAGCTTACTATTGAACTTGGAGTTTTGGAGGAACTTCAGGCAGTATTTAATCCAGAAATGGCTTATGCATCTTACATTCCTTTCTACTGTCTCATTGGTAAAAGACATTTGTACTTGTTCGTTTTACCAAAACACATTTTATAAATATCTGTTTAACATCTTTTGTTTTGTTTTTTAGGTGATTCAGGAATTCGCAAACTTGTTACAAATCATGAGCTAGTTTGGAGTCTGGCTCAGTCTTACCACGAACGAGCAAGTCCTGGTAGCCCAGAATCCAACCCAGTTGGTGGTCAGAGAGCCTCTGCTGTGGGCCTTTCTCCTAGTATGGGCCGCCAGATGAGTCGCAGTCCCTTTCCTGCTCCTTCATCCACTTCCACACCACTAGGTGGAGACATATTACCTGAGTCGGGAACATTTGGCAGTCATCTGGTAGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14473
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 |
---|---|---|---|---|---|
ENSDART00000111927 | Essential Splice Site | 1570 | 2065 | 8 | 11 |
Genomic Location (Zv9):
Chromosome 15 (position 25898098)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 26628881 |
GRCz11 | 15 | 26561757 |
KASP Assay ID:
554-6794.1 (used for ordering genotyping assays)
KASP Sequence:
CCAAAACACATTTTATAAATATCTGTTWAAMATCTTTTGTTTTGTTTTTT[A/C]GGTGATTCAGGAATTCGCAAACTTGTTACAAATCATGAGCTAGTTTGGAG
Long Flanking Sequence:
GAACTCGGGGAGAACATGCAAACTCCATACAGAAATGCCAACTGACCTAGTCGAGGCTTGAACCAGTGACCTTCTTGCTGTAAGGCGATTGTGCTACTCTCTGTGCCATCGTGATGCCTGTTTGATTTCATATCAACCTTAAATATTGGCTTATTTTAAAAGAATCCTCAGAGAATTGTTAATATTTAGCTGATGCAGTTTGAGATCCTTTAACAACATTATTTAATAATATTAAATCCTTTTCTTTTGGTGCAGATTGGAAGTGCCCCACGTAGGGAGGTTGCAGAGTGCACATACCTGGACTTGCGCATTCCAGATGGAGCAGAGCTTACTATTGAACTTGGAGTTTTGGAGGAACTTCAGGCAGTATTTAATCCAGAAATGGCTTATGCATCTTACATTCCTTTCTACTGTCTCATTGGTAAAAGACATTTGTACTTGTTCGTTTTACCAAAACACATTTTATAAATATCTGTTTAACATCTTTTGTTTTGTTTTTT[A/C]GGTGATTCAGGAATTCGCAAACTTGTTACAAATCATGAGCTAGTTTGGAGTCTGGCTCAGTCTTACCACGAACGAGCAAGTCCTGGTAGCCCAGAATCCAACCCAGTTGGTGGTCAGAGAGCCTCTGCTGTGGGCCTTTCTCCTAGTATGGGCCGCCAGATGAGTCGCAGTCCCTTTCCTGCTCCTTCATCCACTTCCACACCACTAGGTGGAGACATATTACCTGAGTCGGGAACATTTGGCAGTCATCTGGTAGGAAACCGCATCCAGGTAACTAGAGACACTGAAGCCTGTGGAAGTCCTAACTTGTCCTCTTTGGAAACGTGGACACATGGACGACCTTATGGTAGCAATGCACCTCCAATGAGTCTAGCCACCACTGCACTTTCTTCAGCTGGACCTTCTTTTTCACATTCGTCATACTCCTGGGTAATGGGACCCACTCCAGAGGACAGTGCACTAAAACAGGACCTTCCACGTAGCAGCCGCTCACTGCAGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11031
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 |
---|---|---|---|---|---|
ENSDART00000111927 | Essential Splice Site | 1570 | 2065 | 8 | 11 |
Genomic Location (Zv9):
Chromosome 15 (position 25898098)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 26628881 |
GRCz11 | 15 | 26561757 |
KASP Assay ID:
554-6794.1 (used for ordering genotyping assays)
KASP Sequence:
CCAAAACACATTTTATAAATATCTGTTWAAMATCTTTTGTTTTGTTTTTT[A/C]GGTGATTCAGGAATTCGCAAACTTGTTACAAATCATGAGCTAGTTTGGAG
Long Flanking Sequence:
GAACTCGGGGAGAACATGCAAACTCCATACAGAAATGCCAACTGACCTAGTCGAGGCTTGAACCAGTGACCTTCTTGCTGTAAGGCGATTGTGCTACTCTCTGTGCCATCGTGATGCCTGTTTGATTTCATATCAACCTTAAATATTGGCTTATTTTAAAAGAATCCTCAGAGAATTGTTAATATTTAGCTGATGCAGTTTGAGATCCTTTAACAACATTATTTAATAATATTAAATCCTTTTCTTTTGGTGCAGATTGGAAGTGCCCCACGTAGGGAGGTTGCAGAGTGCACATACCTGGACTTGCGCATTCCAGATGGAGCAGAGCTTACTATTGAACTTGGAGTTTTGGAGGAACTTCAGGCAGTATTTAATCCAGAAATGGCTTATGCATCTTACATTCCTTTCTACTGTCTCATTGGTAAAAGACATTTGTACTTGTTCGTTTTACCAAAACACATTTTATAAATATCTGTTTAACATCTTTTGTTTTGTTTTTT[A/C]GGTGATTCAGGAATTCGCAAACTTGTTACAAATCATGAGCTAGTTTGGAGTCTGGCTCAGTCTTACCACGAACGAGCAAGTCCTGGTAGCCCAGAATCCAACCCAGTTGGTGGTCAGAGAGCCTCTGCTGTGGGCCTTTCTCCTAGTATGGGCCGCCAGATGAGTCGCAGTCCCTTTCCTGCTCCTTCATCCACTTCCACACCACTAGGTGGAGACATATTACCTGAGTCGGGAACATTTGGCAGTCATCTGGTAGGAAACCGCATCCAGGTAACTAGAGACACTGAAGCCTGTGGAAGTCCTAACTTGTCCTCTTTGGAAACGTGGACACATGGACGACCTTATGGTAGCAATGCACCTCCAATGAGTCTAGCCACCACTGCACTTTCTTCAGCTGGACCTTCTTTTTCACATTCGTCATACTCCTGGGTAATGGGACCCACTCCAGAGGACAGTGCACTAAAACAGGACCTTCCACGTAGCAGCCGCTCACTGCAGGG
Associated Phenotype:
Not determined