ZMP
wwox
Ensembl ID:
ZFIN ID:
Description:
WW domain-containing oxidoreductase [Source:UniProtKB/Swiss-Prot;Acc:Q803A8]
Human Orthologue:
WWOX
Human Description:
WW domain containing oxidoreductase [Source:HGNC Symbol;Acc:12799]
Mouse Orthologue:
Wwox
Mouse Description:
WW domain-containing oxidoreductase Gene [Source:MGI Symbol;Acc:MGI:1931237]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa9191 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa44361 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa38145 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa32547 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa9191
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 |
---|---|---|---|---|---|
ENSDART00000020806 | Nonsense | 85 | 384 | 4 | 10 |
Genomic Location (Zv9):
Chromosome 25 (position 38094583)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 36496372 |
GRCz11 | 25 | 37067261 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GATGTMTYTTTCCCTCTTGTCCTCAGTCACATCAACAAGCGTAAGAYGTA[T/A]TTCGACCCTCGGCAGGCCTTCACTGTAGAGGACATGCAGGTGAAGCCTAA
Long Flanking Sequence:
TGAAAGATTCCTGCCATGAAAATAGCCTTGGTTGCTGACATGGCACTAAATAAAAAATACATTACATTACATTACATCCTGCCAAACTGAAAGAAATAGGATTTTTACTAGAAATAAAAATATAATGGCAAATACTGTGGAAAAAAAAATCCTAGCTCTGTTGGAAAATATTTGAAATAAAATAATTTTAACCTTTAAAATGGGTTTAAAACTATTAAAAACTGCTTAAATTTTAGCCGGGAAAAAAAAACAATTAAGACTTTCTTCAGAAGAAAAAAACATTATAGGAAATACTGTGAAAAATTCCTGAATCTGTTCAACATCATTTGGGAAACATTTGAAGAAATTCACACGACAATGAATAACTTTGACTCAAGCTATAGTTTTTTTTCCATGTCTCTCCAGTATAATTTTTTTTATACTATTTTATTGATATAATCTGACTTTATTGATGTCTCTTTCCCTCTTGTCCTCAGTCACATCAACAAGCGTAAGACGTA[T/A]TTCGACCCTCGGCAGGCCTTCACTGTAGAGGACATGCAGGTGAAGCCTAAACGCTACGACGGAAACACCGGCGCTCTGGAGATCCTGCATGGCCAGGACCTGTCCGACAAGGTCATCATCGTCACCGGAGCCAACTCTGGCATCGGTCAGTGTCACAAAACACATATTCATTTAGCAGATACTCTCATCCAGATCAAGATAAAAGAAGAACTGCAGATCACCAGACAGCAGAAATATGTAGTATTACAAACAAGCAGGACGAAACGCACACAGACACAAGCATTCACAAAGAGGCTGAGCTGTGCTTCAGGGTTTGTCCAGCAGGTGGAGCTGCAGGATTGAGGATTTTCACTCCTTGAGTTCTAATCAGTCAGTCAGGGATCAGGTCTATAGATGTGGATGATTATTATTGCAGGTATATTTAACGTGTAAAAATGCTGCTTTTGTGGTGAATTTTATTTCTTAAACTGTGTGACCGCTGTTGATTCACATGTGTTTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44361
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000020806 | Essential Splice Site | 199 | 384 | 6 | 10 |
Genomic Location (Zv9):
Chromosome 25 (position 38016114)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 36417989 |
GRCz11 | 25 | 36988878 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTCTGAGGAGCGTCCGACAGTTCGCAGAGCTCTTCAAAGCCACAAAACT[G/A]TGAGTAAAACACTGCCGAAATAAAGCAGATCCATCAGAGACTCAACAAAC
Long Flanking Sequence:
ATAATCAAAGAAAAAAAATGATAAATAAAATAAAATAAAAAATAATTAAAATAAACTGAAAAATAAATAGCAATAAAAAAGTTAGTTGGTTTCCTGGCATGTGTGTTAACCTGAGGTGACAGTGTCATGACCTTTGACCCCTGTGCATACACTCTTCTTCAGGCCAGTGATTTATGTGTCCTCCTGAAATCGATCTTGTTCTGTTCTGATCAAAGCTGCACTAAAAGGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTAGAGTAAAGCATTACAGTGCTCATCCATTATGCATTCGCGTCCGCTGTCATTATATGCCCATTATACTATAGTAACGCTGCTCTTGTGTTTCTCTCTGCAGAGCAAAGCCCGTGTGGAAGTTTTACCGCTGGATTTGGCATCTCTGAGGAGCGTCCGACAGTTCGCAGAGCTCTTCAAAGCCACAAAACT[G/A]TGAGTAAAACACTGCCGAAATAAAGCAGATCCATCAGAGACTCAACAAACACGCAATAATCCACATCCTGAAGCTCAAACCTGCTGAATTCACTCAGCATAACAGTTTTAATAACTCTAATAACTGATTTTTTTTTTCTCTTTGCCATCATGACAGTACATATTATTAGACTATTAGACAATATTAGACTAGATATTCTTCAAGACACTAGTATTCAGCTTGAAGTGACATTTAAAGGCTTCACTAGGTTAGGGTAATTAGGCAAGTCATTGTATAACAGTGGTTTGTTCTGGAGATTATCCTAAATTAATATTGCTGAAGGGGGCTAGTTGTCACTGCCAACAGCAATCCAGCCTGTGTGCATCGCTGAAGAACTACAAATCTGCCACTTTAAAGAACTACACATCCAGTCATGCACCACTCACACGCACCTGTTCCTAATTTGATTGATTACACACACACACACACATGGCTGGAAGATGTTCATGAACTGATTAGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38145
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000020806 | Essential Splice Site | 261 | 384 | 7 | 10 |
Genomic Location (Zv9):
Chromosome 25 (position 38002396)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 36404271 |
GRCz11 | 25 | 36975160 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGGCTCTCGGCTCCGGCACGGGTCGTGGTGGTTTCCTCCGAGTCCCACAG[G/A]TCAGCATTTCACATCATTCCTGCAGACGTATGCAGATATTCAGTAATTCT
Long Flanking Sequence:
TAAAGACCCTTGTACACCACAAAGGCCTTGCAAAATGTACAACTTGATTATGACATTCCGTTACGTAACACTAGAGAATATTAAAATGGAATGGATAGAACAACTAGGAATTAATGTTTCAGATAAAGCAGTTGATATTATAAACTAGACTTCATCATGTGCGCGTCTTAATCTGATTCAGATGACATTTTTGTTCCATATTCAGTACAGCAAAACCAAACTGGCTAAAATCTTTATAGTATTTGTTAATTGTAGTCTTTTATAGTTTGTCTATGTTGTACTTCAGAATGAGAGTGTTTTCCTTCTGTTTTCAGGCCTCTGCATGTGCTGGTGTGTAACGCTGCCGTCTGCTCACAGCCCTGGCGTCTGACGGAGGACGGGTTCGAATCCACCTTTCAGATCTGCCACCTGGGCCACTTCCTCCTGGTGCAGCTCCTGCAGGACGTCCTGCGGCTCTCGGCTCCGGCACGGGTCGTGGTGGTTTCCTCCGAGTCCCACAG[G/A]TCAGCATTTCACATCATTCCTGCAGACGTATGCAGATATTCAGTAATTCTATACACTGTATTTTAATGATGAACATGCACAGGATTGATATTGAGGACACTGCAAAAAATACAGGGGTTGGACAATGAAACTGAAGCACCTGGTTTTAGAGCACAGGAATTCATTGGTGTAGCTCCTCAATACACCATCAAGTGGCAGGTTCAAGTCCTGCACAGCGGCCAGAAGGATTTTGAGCCGTTCTTCTTCAGAATAGTGTTCAGGACACTACTGATGCTGCTGGAGGCAAAACTTTCCTGACTCGCTCCTCCAAAACAGCCAAAAATGCTCAATAATGTTTAGATCTGGGTACTGTGCAGGCCATAGGAGATGTTTAACTTCACTTTTATCTTTATCAGACCACTCTATCTATCTCTATCTACTGTCTCCAGTCCTTCTGTTTGTATTGCTGCATTATCGTCCTGAAACACACCACCGCCCTCTTGAGACGATGTTTGATCCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32547
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 |
---|---|---|---|---|---|
ENSDART00000020806 | Nonsense | 292 | 384 | 8 | 10 |
Genomic Location (Zv9):
Chromosome 25 (position 37994140)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 36396015 |
GRCz11 | 25 | 36966904 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCTGCTGTCTCCTCCACAGAAGAACTACTGGTCTCTGCTGGCCTACAAC[C/T]GAGCCAAACTCTGCAACCTGCTGTTCTCCAGCGAGCTGCACCGCCGCATG
Long Flanking Sequence:
AATTCAGTTCAATTCAATTTTCCTCAGTTCACTCCACCCAATTCAGTTCAGTTCACTTCTTCAATGCATTACATTAATTTCACTTTAATTAATTTTCAGTTCAATTCAGTTCACTTCTTCACTTTAATTTAATTCAGTTCAGTTCACTCCAGTTCATGCAATTCAGTTCAGTTCATCTCAACTAAGTTCACTTCAAATAAGTTCAATTCAGTTCACTTCAACTCATTCAATTCAGTTCTCTACACTTAAACTCCATTCAGTTCAATTTACTTCTTCAGTTCACTACATTAAATTGTCAGTTCGATTCATTTCAGTAAGTAACTAAACTCGATTCAGAATTGCTTCATTGGCACGACTGTGGAAAAACCCAGTATTGTCAGAGTGTGAATGTGTTTGTCTGTGTGTGCAGGTTCACAGATCTGCTGGACTCGTGTGGGAATCTGGATCTGGATCTGCTGTCTCCTCCACAGAAGAACTACTGGTCTCTGCTGGCCTACAAC[C/T]GAGCCAAACTCTGCAACCTGCTGTTCTCCAGCGAGCTGCACCGCCGCATGTCCCCGCACGGCATCTGCTGCAACGCTCTGCATCCCGGAAACATGATGTTCACCTCCATCCACCGCAGCTGGTGGCTCCTCACGCTGCTCTTCAGCCTCGCGAGACCCTTCACCAAGTCCATGGTAAGAGCTGGAGGTTACTCTGTTTTACAGCATGAGCTGCTGTGGGGTTGATAAAGGGTGTCAATGGAAGATTTTGAGGCGTTTTTTTAATGTCTGGAAGAGCTGTGCAGTGAAGTGGTTTTGTCTCAGTTTTTGTGGATCTGTAATTCGTTACTTGAGGTTTGATTAGTTGTAGCTTTCTGATGACAAATCCACTAGAGGGCGATGTTTAAGTTTTTGAGTTTCTGGAATGTTACAAAGGGTTTGTTTTGTTGCTCATTTCAGGTGACAAATCCACTAGAGGGCACTCTTAACATTTTGAATATGTACTTTGTTATTAATGGTTTG
Associated Phenotype:
Not determined