ZMP
zgc:55695
Ensembl ID:
ZFIN ID:
Description:
exosome component 10 [Source:RefSeq peptide;Acc:NP_957383]
Human Orthologue:
EXOSC10
Human Description:
exosome component 10 [Source:HGNC Symbol;Acc:9138]
Mouse Orthologue:
Exosc10
Mouse Description:
exosome component 10 Gene [Source:MGI Symbol;Acc:MGI:1355322]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa39400 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa43927 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa24276 | Nonsense | Available for shipment | Available now |
sa24277 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa39400
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000054915 | Essential Splice Site | 128 | 499 | 3 | 27 |
ENSDART00000137410 | Essential Splice Site | 128 | 899 | 3 | 25 |
Genomic Location (Zv9):
Chromosome 23 (position 14886368)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 15018301 |
GRCz11 | 23 | 14774378 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCGCTTTGACCTGGTGGTGGACGCAAATGATGCCATCCTGGAGAAAGTGG[T/A]ACGAGTCTCTCACTGACACGCACACATCGCTGAAGTTCTGGTTCAGTGCT
Long Flanking Sequence:
TATTTATATATGCTTGTAATTTATTATGATTTATGCAAACGCACTGGACAGAAACAGACTTGATCATCTCAATCTATCTAAATGAATGAAATCTTTCCAAATCTAGCTATTCTATTCATCTGGTAAAATTATATTCATTGATAGTATATATGAATAGTAAATATTGCAAAAAAAAAAAAAAAAAAAAAAAATTCTATATATATTGCAATGTCAGATTTTTCCAATATTGTGCAGCCCTACTACTAGGTATTCTTAAATATATATGCCACAGCATACTGCATAAAGCTTATCATGTCAGTGTCAGTAAAGTTTACTTCACTGGAGACTGACAAAGCAATTTTCTTTTTTTTCTTTTTCTTTTTTTTTTCCTGACAGTATGAGCCAGATAATGCAGCACCATGGCTGTAGATCCCACATGAGAGACCGGAACAAACTGACTGGACTGGAGGACCGCTTTGACCTGGTGGTGGACGCAAATGATGCCATCCTGGAGAAAGTGG[T/A]ACGAGTCTCTCACTGACACGCACACATCGCTGAAGTTCTGGTTCAGTGCTTCCTGTTGGCATGTCTGTTAATGCTGAGAATGAGAAGGTTTATTCCAGACACTGAAAGTCAGGGAATGCTCATATATTTTTGTTAATCTCCTGGAATATCAGTGATTATTGTGTTATTGCTTTAAATTTTAGTTTCCATTCAGCAAAATGCAACTTTTCTGTACCATATTCACATCTATAGTTACTCTCATCAACTCCCAGTCATTTAACTAAGGCTAACATGTTGGGACAATATACATTGTAAGAGATTTGGTTTCAAATGACAACTTCAAAAACTTTGTCAGAAGTAGACCTCAGGAATTTGTTAGGCTATCATATGTGGGAGAGAGAGCAAATTTGTTTTAATATTTGAATTATACTAAATTATTGATTGTTCTTATAATGCCTGTTAAAACTTAAAATGATATTCAGATTAAAATAATTCTTAAATTATTTTCTTATCTATCCATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43927
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 |
---|---|---|---|---|---|
ENSDART00000054915 | Essential Splice Site | None | 499 | 21 | 27 |
ENSDART00000137410 | Essential Splice Site | 744 | 899 | 20 | 25 |
Genomic Location (Zv9):
Chromosome 23 (position 14908722)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 15040655 |
GRCz11 | 23 | 14796732 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAGGCTCAGGCCAAACAGCAAGCTAAAGAACAGGCCAAGAAAGCTCAAG[G/A]TACAAACAACACAACTCTGGTGTGCAACGCTAAAATAAACTCTCTTTCTG
Long Flanking Sequence:
ATGAAATGCAAAGGTGTTAAGGCTATGGTTCCCCCCTAAATGAACATTTACTCACTATTCACTATCCCTCTAATGGTTCCAAACCTTTGAGTTTCCTAATTCTGAATAAAAAGTTATTTACCTGTAACCAATGACTTCCTTGGTAGGAAAAATAAATACTATTCAAGTCAGTGGTTGCAGTTTTTTAGATTTTCTTTTGTGTTTAACAGAATAAAGAAACTCTAATTACTTTTTAGCAAGTAAATAATGAGTAAATGATTTGAAATTTCAGTTTTGGGTGAAATATTTAAGTTGAATACGAAGCCACTGTTTGAATGTCAAAAATTCAGGAACTCTTATTATCTTATGGTTGTTTTTTTCCCACTAAGCCACATGAAATTTAGTTTTGTTGCTCTGTTTAATGCAGATTCATAACCGGTGGAAACTGCAGAGTATTGAGCAGCAGCAGAAAGAGGCTCAGGCCAAACAGCAAGCTAAAGAACAGGCCAAGAAAGCTCAAG[G/A]TACAAACAACACAACTCTGGTGTGCAACGCTAAAATAAACTCTCTTTCTGTGATTGTCATTTACTCATAGGCAAAGTAATAAGATGTTTGTTCTTCACAATACACTAAAATTACAAAAATATAAAAAGAAAATACCAGCGTGTGGCATCAAACGCTATAGTGAGCTGTTTTGTATGGCAAACTATTAGGGATGCGCAGAATATTTGACTGCTAAAAATTCTCAGATAAAATGGGCATTTTTGGTTTTGAGCTGAAGGAGAATTCACTATCCGTCCAGCCGTCATCACTGCGGCATGTATGGCCTGTGGGTCAGCAGATTGAAGCCCCTGCTTGATACACAACAAACTCCATTGTAGGTCACCTTTCACAGTTTTATCTCATTATTTTAAACATTCTCACAGATATCTTTTCACAGAAATAAAATGTATCTGGAGTAACAGTAAAAAAACGTTTAAATATAAAAATGTAAATATGTAAACACTTTTTAAAAATATAAACCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24276
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 |
---|---|---|---|---|---|
ENSDART00000054915 | None | None | 499 | 22 | 27 |
ENSDART00000137410 | Nonsense | 747 | 899 | 21 | 25 |
Genomic Location (Zv9):
Chromosome 23 (position 14911288)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 15043221 |
GRCz11 | 23 | 14799298 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTCCTTAAGATTTATGTCCTAAAATGTTTATATTTGTGTTTCAGAGGAA[C/T]GAAAGAAAGCCAAACAGACCTACCAAGAGTCGCTTCAGAACGTTCACACC
Long Flanking Sequence:
CACAAACCACACATGCTCAGCGAAAAAGCAATGTCTGCTCAATAATGCAAGAACAGGACATACAGTATACTATGTAGTATACTTGTTCTTGCTGCTTTCACCAGTGCTACTGTGTTTTAATGGCAATGCTGTGACAACTCTTGACTCATTGACTGTCAGAGCAGCTTAACTTAGCAGCTTGGTGTTTAGTTTTTGATTGTCTTTTTAGAACAGTTTAAATTTGAGTTAAATTTACAAAATGTCTTGTGTAATAAAATGCTAAATAATAATTTTAAAACATTTTCAGTTTTGGTTTTCAATCAAATCCAGATCCAGTATTTTCATTTTGGTGCATTCCTTTAAAAAAAAAATCTGTTGAAGTGAATGAGTCCGGAAGTCTCAACATATGCACAATACCCCGCAACTGCTCTATTGTGAAAAATAAAGTGGATACAAACTCTGCTAAGCCACCTTCCTTAAGATTTATGTCCTAAAATGTTTATATTTGTGTTTCAGAGGAA[C/T]GAAAGAAAGCCAAACAGACCTACCAAGAGTCGCTTCAGAACGTTCACACCGTCAGAGAGCAAGTGAAGGTGAGGAGCTCCACTTCACCACATTTGTTTATTTCATCTTCATCTTTCACTAACATCTGTTAACAATCTTGTGTTTTAAGGAAGCAAAGCAGGCTGGACAGAAAAGAGAAAGAGCTGCAAGTGATGTCAGCGAAGACAGTCTTAAACCAAACGTCAAACTCTCAAAGAGCGAAGGTGAGACAACGGTGGCTGATCAGTCTACAAAACCTGCAAAGAAGAAACAGAAACAGAAAACGGCTCAGGAGCCCGAAGCTCCCAAACAAGACTTTAAACCTTACGACTACAGTCAGTCCAATTTCAAATTATTCGCCGGTGAGTGATCTGCCATGTTTTATTTTCTTAAAGCAATAGTTTGAATTTCACTAAACAAGATATCTTGAAGAATGTTGGATAAAACAGCCATCGACTTCCTAAGTATTTTTTAGTTCCTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24277
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 |
---|---|---|---|---|---|
ENSDART00000054915 | None | None | 499 | 24 | 27 |
ENSDART00000137410 | Nonsense | 861 | 899 | 23 | 25 |
Genomic Location (Zv9):
Chromosome 23 (position 14912020)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 15043953 |
GRCz11 | 23 | 14800030 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACACACAGGTAAATCAAAAGACGGCTCACACTTTGATCCAAACAGACAA[G/T]GACCCAAGCAGAAGGTATGAAGTTCTGTTGTTTACACTGCTCCACTCATT
Long Flanking Sequence:
AAAGAGCGAAGGTGAGACAACGGTGGCTGATCAGTCTACAAAACCTGCAAAGAAGAAACAGAAACAGAAAACGGCTCAGGAGCCCGAAGCTCCCAAACAAGACTTTAAACCTTACGACTACAGTCAGTCCAATTTCAAATTATTCGCCGGTGAGTGATCTGCCATGTTTTATTTTCTTAAAGCAATAGTTTGAATTTCACTAAACAAGATATCTTGAAGAATGTTGGATAAAACAGCCATCGACTTCCTAAGTATTTTTTAGTTCCTATTATTGAACATATTGAATATTATTGGCTGTTTATTTCCCTTATGTCCTTTAAAATATCTGGTTTTGGGTTTAACAGGAATTCATGAACACTTGAGGAAATAGTGCAGAAATTGTCTTTGTTTTTGGGAGTGATCTGTCTTATTAAGACTCTTCAGTGTGTTTTCTTCATTGTTTGTCTTTAATACACACAGGTAAATCAAAAGACGGCTCACACTTTGATCCAAACAGACAA[G/T]GACCCAAGCAGAAGGTATGAAGTTCTGTTGTTTACACTGCTCCACTCATTTCTGTTCTGTTGACATTTTAGTCAGATCACATGTAGATAAGGGAGACTTTCACTTTCAATCCAACAGCTTCATTAGCCGCGTTTCCACTGTTGTGCCTAAATTAAGCGTGCCAGGCCAATCGCTTTTCCACTGTCACTACCAGAGCCTGATCGTGCCAAAGTGTTGCTTCCTCTGGGCCAGCGTCAAGGCCTTTTTCAGCTCACCAAATACCTTGGGCAAAGAGGGCCAGCTAGGGTGGAGGGGCGGATGGAGAGGCGGAGTTTGCCCCAGTCTATTAGTCCGACAGTGGAAACGCAACATGATTTCGGCCTCAGTGCTCATGCTCCCGGGCTATTGGCATGGCCTGGCCCAATAAAAGCCCTGTCTCACACTGGTCCGACAGTGGAAATGCTGCTATTGAGGATGTTTTAGTAGGTATATTATAATGTAAAATAATAATAATATAATTT
Associated Phenotype:
Not determined