ZMP
si:dkey-175m17.7
Ensembl ID:
ZFIN ID:
Human Orthologue:
DUSP10
Human Description:
dual specificity phosphatase 10 [Source:HGNC Symbol;Acc:3065]
Mouse Orthologue:
Dusp10
Mouse Description:
dual specificity phosphatase 10 Gene [Source:MGI Symbol;Acc:MGI:1927070]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa43659 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa23954 | Nonsense | Available for shipment | Available now |
sa7482 | Missense | Mutation detected in F1 DNA | Not yet available |
sa1705 | Nonsense | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa43659
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109626 | Nonsense | 215 | 904 | 1 | 3 |
ENSDART00000139058 | Nonsense | 215 | 892 | 1 | 3 |
Genomic Location (Zv9):
Chromosome 21 (position 26678090)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 27247001 |
GRCz11 | 21 | 27283696 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTACAGTATCTCCTGGAGGAATATTGGAGTTTGTACCAGCTCAAAGACAG[C/T]AGTCAAAATCCAAACCAACAAGAGAGAGAGACTTGTCATCAAAGACTTGC
Long Flanking Sequence:
CACAACCCCAACCCCCACCACCCCGTTCCTATCCAGGTTCCAACTACCTGTCTCTGGAATGCAAGCGCAGGCAGCCGTCCCATGTTCAGAGAGATAAAGGGGAACGAGGTGCTCTCTTCGAGGAGAGTGACCACAATGCTAGTCATTGTCACAGCAATGGGACTGTGACTTTAGGTCCCAGACCTCACAAGCACACACATACCATTGACATTAAAGTGTCTTTGGACAAAGGTGGAAGAGGGGGATCTTACATAGAAAAAGGTCGCAGCAGCAGTCTTACCCGAAGTGAAAGCATCAAGGGGAGCAGAACTAAAAGGGTGTCCCTGCACTTGGACTCTGGGCAAGGTGAAAGAAAATGCAAAGGAAAGTCTTCCGAGTTAGTGGAGAAGCATCAGAACTATCATCAAAGTCAAAACAGGACTCCGCACAGTAGCCATCTTACAAACCAACTTACAGTATCTCCTGGAGGAATATTGGAGTTTGTACCAGCTCAAAGACAG[C/T]AGTCAAAATCCAAACCAACAAGAGAGAGAGACTTGTCATCAAAGACTTGCTCTGCAACTGCCAGTTACCCATTGCACAGTGAGAGGGACGCATCATCTGTTGGAAACAAAGAAAACTCCAAACTGGGACCCGGCCACCAGCTGCCCCACGCCCACAGCCTATCCCGTCACCACAGTTCAGCCCCGTTACCTCATGCTGCCATCCTAAACCCTCAGTACCCTGCTGTCCCACCCCCACTCCCTTCCAGAGCCCCTTCCTCCTACCAGCACATCAGTCAGCCCCGTTCGTCACGAATTAGAGAACATCGGCCACAAATTCTTCACGCCTTGCCTCTCTCACCTACATCTTCCCGGGGAGGCTTCCCCAGTCCTGACCATACATGTACGATTGACTTTTCCCACCCCTGTGGCTGTTGGAGGTTGGTGCGTTGTAGAAGAGGTAGAGGTCACACGGCTGGCTGCCACAGTCATAATACAAGCCCATCCTCTTCATTTTCCCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23954
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 |
---|---|---|---|---|---|
ENSDART00000109626 | Nonsense | 319 | 904 | 1 | 3 |
ENSDART00000139058 | Nonsense | 319 | 892 | 1 | 3 |
Genomic Location (Zv9):
Chromosome 21 (position 26678402)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 27247313 |
GRCz11 | 21 | 27284008 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCAGCACATCAGTCAGCCCCGTTCGTCACGAATTAGAGAACATCGGCCA[C/T]AAATTCTTCACGCCTTGCCTCTCTCACCTACATCTTCCCGGGGAGGCTTC
Long Flanking Sequence:
AAAGGGTGTCCCTGCACTTGGACTCTGGGCAAGGTGAAAGAAAATGCAAAGGAAAGTCTTCCGAGTTAGTGGAGAAGCATCAGAACTATCATCAAAGTCAAAACAGGACTCCGCACAGTAGCCATCTTACAAACCAACTTACAGTATCTCCTGGAGGAATATTGGAGTTTGTACCAGCTCAAAGACAGCAGTCAAAATCCAAACCAACAAGAGAGAGAGACTTGTCATCAAAGACTTGCTCTGCAACTGCCAGTTACCCATTGCACAGTGAGAGGGACGCATCATCTGTTGGAAACAAAGAAAACTCCAAACTGGGACCCGGCCACCAGCTGCCCCACGCCCACAGCCTATCCCGTCACCACAGTTCAGCCCCGTTACCTCATGCTGCCATCCTAAACCCTCAGTACCCTGCTGTCCCACCCCCACTCCCTTCCAGAGCCCCTTCCTCCTACCAGCACATCAGTCAGCCCCGTTCGTCACGAATTAGAGAACATCGGCCA[C/T]AAATTCTTCACGCCTTGCCTCTCTCACCTACATCTTCCCGGGGAGGCTTCCCCAGTCCTGACCATACATGTACGATTGACTTTTCCCACCCCTGTGGCTGTTGGAGGTTGGTGCGTTGTAGAAGAGGTAGAGGTCACACGGCTGGCTGCCACAGTCATAATACAAGCCCATCCTCTTCATTTTCCCACGCCCAAGGAACAAGTGCTACCAACGGAGGTGGCGGAACCATGGGCCTGAAGACTTTAGGAGGGTGTCTATCTACTGCTTCCACCACCAACACCTCCTCTTCCAATAGCACTGTCTCAGATTGTCGTACAGGACTGCTTAGACCATTAGGTTGTGCATCCTGTTCTGGGGAGGCTGGAGGTTTTGAGAGTCCTGCTGCTTTCCGTAAGAAACTTGTTGGGGGTTGTTTACCCTGTGCCCCCTTGTCCTCATCTGCACCTCTTCGAGCACTCCAGAGTTGCGTCAGTGGGTGCAATCCCAAAGCAAGTCAAACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7482
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:
Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109626 | Missense | 417 | 904 | 1 | 3 |
ENSDART00000139058 | Missense | 417 | 892 | 1 | 3 |
Genomic Location (Zv9):
Chromosome 21 (position 26678698)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 27247609 |
GRCz11 | 21 | 27284304 |
KASP Assay ID:
554-4093.1 (used for ordering genotyping assays)
KASP Sequence:
GGAGGGTGTCTATCTACTGCTTCCACCACCAACACCTCCTCTTCCAATAG[C/A]ACTGTCTCAGATTGTCGTACAGGACTGCTTAGACCATTAGGTTGTGCATC
Long Flanking Sequence:
AAAGAAAACTCCAAACTGGGACCCGGCCACCAGCTGCCCCACGCCCACAGCCTATCCCGTCACCACAGTTCAGCCCCGTTACCTCATGCTGCCATCCTAAACCCTCAGTACCCTGCTGTCCCACCCCCACTCCCTTCCAGAGCCCCTTCCTCCTACCAGCACATCAGTCAGCCCCGTTCGTCACGAATTAGAGAACATCGGCCACAAATTCTTCACGCCTTGCCTCTCTCACCTACATCTTCCCGGGGAGGCTTCCCCAGTCCTGACCATACATGTACGATTGACTTTTCCCACCCCTGTGGCTGTTGGAGGTTGGTGCGTTGTAGAAGAGGTAGAGGTCACACGGCTGGCTGCCACAGTCATAATACAAGCCCATCCTCTTCATTTTCCCACGCCCAAGGAACAAGTGCTACCAACGGAGGTGGCGGAACCATGGGCCTGAAGACTTTAGGAGGGTGTCTATCTACTGCTTCCACCACCAACACCTCCTCTTCCAATAG[C/A]ACTGTCTCAGATTGTCGTACAGGACTGCTTAGACCATTAGGTTGTGCATCCTGTTCTGGGGAGGCTGGAGGTTTTGAGAGTCCTGCTGCTTTCCGTAAGAAACTTGTTGGGGGTTGTTTACCCTGTGCCCCCTTGTCCTCATCTGCACCTCTTCGAGCACTCCAGAGTTGCGTCAGTGGGTGCAATCCCAAAGCAAGTCAAACTGGCAGCTCCACATGTAGCTACTGCAGTAGTGACCCCATTGTAGTTACCTTTAACCCACACAGAGGGAATCCTCCTAACATGGGCCATAATGTTGGCGCACATACCATGGGCGGATACCAGCCCGATGATGACGATTACAGTGTACGCACAATTTGGCCAGAGGAACTAGCAAAGAAGATGACTCGTTCGAAAACCCAACCTATCCACCACAATTCAGGCTCAGGGAGGACCTGCATGGGCCACAACCAGAATAGTGGCAATGGTGGCAATCCTGTAATCCTTGACTGTCGGAATCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1705
Status:
F2 line generated
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 |
---|---|---|---|---|---|
ENSDART00000109626 | Nonsense | 808 | 904 | 2 | 3 |
ENSDART00000139058 | Nonsense | 796 | 892 | 2 | 3 |
Genomic Location (Zv9):
Chromosome 21 (position 26680469)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 27249380 |
GRCz11 | 21 | 27286075 |
KASP Assay ID:
554-1651.1 (used for ordering genotyping assays)
KASP Sequence:
TACAAAAGRCTCCCCGCTACTGACAACAGCAAGCAGAACCTGCGACAGTA[T/A]TTCGAAGAGGTTTTTGAGTTTATAGGTAAGAGAACGTGTCAACTTTTGTA
Long Flanking Sequence:
AGAGTGAAGAGTCTTCAAACAGGAAAGTTAAGGAGGAGGGATTAAAATTAGTAGAACTATTCGATTTCCTTACATAAGGGCTCTATGACATTATGTTTCAGCAGCATTTTAACCTGTGCCATTTCTAAACGATTGAAAAGAGTCTAAAAAACTTTACATTCTTATCTCATTATACAAACTAATTTAAGCAACATTTTATTTTATTGTTTGTTTTTTCCAGTGCACCTTTCGCTCCCTCTTTCCTCCTCACTCCCAGCATCACTGTCTGACGAGAGTGTGATGACTCCTGATGTGGAGAATGCTGTGATTAGTCCCATCCTCCCTTTCCTTTTCCTGGGCAACGAGCGAGATGCACAGGATCTAGATCTACTTCTTCATCTTAATATTGGTTTTGTGGTCAATGTCACCACCCATCTTCCCCTCTACCATCTGGACACAGGCTTGGTGCGTTACAAAAGGCTCCCCGCTACTGACAACAGCAAGCAGAACCTGCGACAGTA[T/A]TTCGAAGAGGTTTTTGAGTTTATAGGTAAGAGAACGTGTCAACTTTTGTATTTGACATATTCCCAGACTCCATGAAAATGTCTTGGTATGGATAAAGTGTATCAAAAGGCTTGTCTTTTTCTTTTTTAAACTGTTAATAGCCTTTGGCAGTGAACAATTATTTTTAGTTCAGGGGTGTCCAATGCTGCTCCTGATGGGGCAGAATTTTAAAAAATTTAAGCTCCAACACATGTACCTGGAAGATTTTAGTAAGTCTGAAGGCCATGATTAGCAGATTTAGGCTTGCTAGTGTTGGTTGTAAACTCCTCTCTTCTGGACATCCACCCTCGAGGATGAGTTTTGGACATGTTTAAGCTAGTCCGGTACAGGTGGTACTATGGAAGTGGGGCATTTTATTTGGAATAGAGAACCAAGACTTGGCAAGATGTGTCATCCACAATGTCGGTTTGTGTTCTTGAAAATAATGTTATCAGAACGTCTTTATAGCTAATTTGAATTCA
Associated Phenotype:
Not determined