ZMP
im:7159098
Ensembl ID:
ZFIN ID:
Human Orthologue:
UTP20
Human Description:
UTP20, small subunit (SSU) processome component, homolog (yeast) [Source:HGNC Symbol;Acc:17897]
Mouse Orthologue:
Utp20
Mouse Description:
UTP20, small subunit (SSU) processome component, homolog (yeast) Gene [Source:MGI Symbol;Acc:MGI:191
Alleles
There are 12 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa24757 | Essential Splice Site | Available for shipment | Available now |
sa24758 | Essential Splice Site | Available for shipment | Available now |
sa24759 | Essential Splice Site | Available for shipment | Available now |
sa38162 | Splice Site, Nonsense | Mutation detected in F1 DNA | Not yet available |
sa32555 | Nonsense | Available for shipment | Available now |
sa30375 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa30376 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa44386 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa24760 | Essential Splice Site | Available for shipment | Available now |
sa30377 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa24761 | Nonsense | Available for shipment | Available now |
sa24762 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa24757
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000033957 | Essential Splice Site | 712 | 2788 | 19 | 63 |
Genomic Location (Zv9):
Chromosome Zv9_scaffold3539 (position 13275)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 5872162 |
GRCz11 | 4 | 5880732 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGTGCCTGACATCATTGTTTTGTGTTGTAAATTAAATTACTTTTATTCC[A/T]GGTTCCTCTACGCTATCTTATTGCGATGCTGTTTGTTAACTTCCGACCCC
Long Flanking Sequence:
GTCTTTAATAATTATTATAGTTTTTGCTCTGAAAAAATCGTGTTCATTATTCAGACCTTGCTGTTATCAATATGCAGCTTTTGACGTGTCCATTTGTGATTATTCTTAACAGATTCGCTTGCTGACCCTCAGAATTATGACAAACTTTGAGGCTGATCTTCCTAAACCAGCAGAGGTATCGTTTGTGAGTTTCCTCAATCACAGCAGATGTGAAGAAACATGCTTGTGTTAATCAGGAGCTCGTGTTTTATTCAGGAAGAGGAGAGCTCAAATGTGCAGACAGTGTTCGCTGTGTGTCTGCAAGCAGAGCTGGTCCCGGCCACAGTGCAGGACTACAGGGAGAAACTGTTACACCTTCGTAAACTCCGACATGATCTAGTGCAGGCCTGTCTGCCTAAAGGAGCTTTCCATGAGGTAGCTAATGCATTTTACATCATGTCTAGTATTAAATTGTGCCTGACATCATTGTTTTGTGTTGTAAATTAAATTACTTTTATTCC[A/T]GGTTCCTCTACGCTATCTTATTGCGATGCTGTTTGTTAACTTCCGACCCCTCTGGGATGCTGTTATTGAGCTATTGGAGTAAGTGCTTCATTATTAGTTATTGCTGTTTCACTGCATTATTTCAGTTTTTTCATGTTTGTTTAACATGCATTCATCCGCTCAGGTCCCACGCTAAAGAAATGGACAATAAGTCATTCTGGAAGGTCTATTATGAACATTTGGAGATGGTTGATAGTCTTGCTGGTAAGTTCAAGGGATGCCAACTCATTTATCTTGTGTTGATGTTGCAAATTTAGGCCATGTTTACACAATTATTTAGCCAAAAACTGAAAAAAAACTTTTTTCTTTGGGTTTAAAAAAACTTTCACATAAACATGACAACAATTTTTAGATCATTAATTACCAGAAACTGCTGTATTATGGATGCTAGGACAGTATTTGGTGCTGTAATCTTGTTAGTAAACAGCCCCTATAGCTGGGGTGTGCAAACTCTGTCGTGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24758
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000033957 | Essential Splice Site | 712 | 2788 | 19 | 63 |
Genomic Location (Zv9):
Chromosome Zv9_scaffold3539 (position 13276)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 5872163 |
GRCz11 | 4 | 5880733 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGCCTGACATCATTGTTTTGTGTTGTAAATTAAATTACTTTTATTCCA[G/T]GTTCCTCTACGCTATCTTATTGCGATGCTGTTTGTTAACTTCCGACCCCT
Long Flanking Sequence:
TCTTTAATAATTATTATAGTTTTTGCTCTGAAAAAATCGTGTTCATTATTCAGACCTTGCTGTTATCAATATGCAGCTTTTGACGTGTCCATTTGTGATTATTCTTAACAGATTCGCTTGCTGACCCTCAGAATTATGACAAACTTTGAGGCTGATCTTCCTAAACCAGCAGAGGTATCGTTTGTGAGTTTCCTCAATCACAGCAGATGTGAAGAAACATGCTTGTGTTAATCAGGAGCTCGTGTTTTATTCAGGAAGAGGAGAGCTCAAATGTGCAGACAGTGTTCGCTGTGTGTCTGCAAGCAGAGCTGGTCCCGGCCACAGTGCAGGACTACAGGGAGAAACTGTTACACCTTCGTAAACTCCGACATGATCTAGTGCAGGCCTGTCTGCCTAAAGGAGCTTTCCATGAGGTAGCTAATGCATTTTACATCATGTCTAGTATTAAATTGTGCCTGACATCATTGTTTTGTGTTGTAAATTAAATTACTTTTATTCCA[G/T]GTTCCTCTACGCTATCTTATTGCGATGCTGTTTGTTAACTTCCGACCCCTCTGGGATGCTGTTATTGAGCTATTGGAGTAAGTGCTTCATTATTAGTTATTGCTGTTTCACTGCATTATTTCAGTTTTTTCATGTTTGTTTAACATGCATTCATCCGCTCAGGTCCCACGCTAAAGAAATGGACAATAAGTCATTCTGGAAGGTCTATTATGAACATTTGGAGATGGTTGATAGTCTTGCTGGTAAGTTCAAGGGATGCCAACTCATTTATCTTGTGTTGATGTTGCAAATTTAGGCCATGTTTACACAATTATTTAGCCAAAAACTGAAAAAAAACTTTTTTCTTTGGGTTTAAAAAAACTTTCACATAAACATGACAACAATTTTTAGATCATTAATTACCAGAAACTGCTGTATTATGGATGCTAGGACAGTATTTGGTGCTGTAATCTTGTTAGTAAACAGCCCCTATAGCTGGGGTGTGCAAACTCTGTCGTGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24759
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000033957 | Essential Splice Site | 976 | 2788 | 24 | 63 |
Genomic Location (Zv9):
Chromosome Zv9_scaffold3539 (position 17831)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 5876718 |
GRCz11 | 4 | 5885288 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCGTTGGACTGTTTGATGACGTACAAAGATCCAAGTATTCTACCCTACAA[G/A]TATGACCTGCACCACATTACATTACTGCTTTAACATTAATTTCATTAATA
Long Flanking Sequence:
GTTTGTTAGAGCATATTGCTTTCTCACTACAACCGAACCACTCTAGAGTTTGTTTCAACCAAGCTGTAACCTCCTTATCCTCAGACTGATTGTTTTGGCTGAGATCAGATTGCGATTGCTGGTTACACATATGCCTAAACGAACCAAGCCAGGAGGTAAACGTGCCAGGTTCCAAAACAAATGTCTAGGTGTGAAAGTGCCATTAAATACTTGCATTTCCTACCTGCATTTATTTTGTTACAGGCAGCTCATTGCTCACCTAAAGGTTTTTTCCAAATTCACCAACCCGAGAGCTTTATATATGGAGGAGAAACTGCGTGAATTGTACATTCAGGTTGGTTCCTTATATTTGTATGACATTCAGTTCTGTTTGCTGAATGTGCTGCTAAAAGCAAACTTTCTCTGAACCCGCAGCTCATGTGCCATAAAGATCAACAAATCCAGAAAATTGCGTTGGACTGTTTGATGACGTACAAAGATCCAAGTATTCTACCCTACAA[G/A]TATGACCTGCACCACATTACATTACTGCTTTAACATTAATTTCATTAATAACTCTGTATTATACAGAAACTAGGTCAGTTTGTGAATAGCATGCCTTAGATTCAGAGCAGTGACTAATGGTATCTTCCAAAAGATGTCTTTGGTTACTTTAGTAACTTTCACTACTGGGATTCCGGAATGTACCAATTGCCTCAGGAAGTCTTTTAGTCTATTTTGGTATTCATTTTTCACATCACTTGAATTACTTTGAGCCAGTTTTTTTGTTTTGTCCATGGAATAAAAATACCTAGATGGGATCCTTTACTGACCTAATTTTAAGAGGATAGCTTTTCTCCAACCACAAACTTGCTCTGTGAATGCTTTAAACAACTTTTAAACATTTTCTAGTCATTTAAATTGTTTTATTATGTAATTATGGTGATTTATATACTGTACATGATAGCTTAAAACTTTAAACATTGCAGCAGTAGCGGTGTACCCCAAGGCTCTGCTTTAGGTCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38162
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:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000033957 | Splice Site, Nonsense | 1144 | 2788 | 27 | 63 |
Genomic Location (Zv9):
Chromosome Zv9_scaffold3539 (position 19472)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 5878359 |
GRCz11 | 4 | 5886929 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCTGCTGTGCATCACAGCCTCTGTGTCATTTATTCTGGATCACAGAGAA[C/T]AGGTGAGCTGACTGCAAAAACAAAAACATCCCAATTAGTTGTTTTATTAT
Long Flanking Sequence:
GTACCTATTGGAAATATAAGACATGATTAATACTACAGACAGTTTTAAAAATTTAGAGAAAGGGGGACATTTTTATTGTTGACCAACCTAAAACAGTAGCAAGCAACAGTACACACTTTCACATCAATAAGTGCAACACATCTGTTATTCCAGAATACTCTGACAAGCTTTATTATAATATTGACAGACCCCTTTTACTCATTTTGCTTAAAAATAAGGAAAGATATATCAAAAGCAGGCTCTGGTCTTGAAATTGCATCATCTGATAGCAGAAAATGTGATTTTTTTCTGCAGGAACGTGCCTGGCGGCAGTAGAAAGAGCTGTAGCTGAGACAAACCTGTCTGCTGTTCTCCCTGTGGGCCGTCAGCACAGTCTGCTTAACACCATAGAAATGCTCATCCATAAGCTGGGCCATCTCATCCACATCTACCTGCCCAAAGTACTGCAGATCCTGCTGTGCATCACAGCCTCTGTGTCATTTATTCTGGATCACAGAGAA[C/T]AGGTGAGCTGACTGCAAAAACAAAAACATCCCAATTAGTTGTTTTATTATGCAAACTAAAATAGTGCATGTAAGGCAAGGCAATAGGGCCAAACACATTTTGTAGCATTTGATTTAGCTGGTGTTAATTGTTTAGACACTTTTTTCAACATAAAAGTTTTGGTGTTAAGGCACATTATCAGATTTTAGAGTAGTATTTTTTTTAATCATGGAGTTTCGTGTCTTTTTTTGTTGCTGATCTAATGAGCTCACTGTTCTTGCCTGTTCCTTTAGCTCAAGCCTGGTTGCATTAATCCGCTAAAGAACTTGCGACGCCTTGGGACTCTGCGCATTCAAGACTTCTTTGATGGCTTTGAGTCCTACAGCTTCACTGCAGATGAGCTAGATGCTGTGTTTCAAGTCATCGTGTGGCCTAAGGTGTGTGAGAAAACTGTCTGAATAACTTTAGTAGCTTTAATAAGCTTCCTAAAATGGGAAAAAGTAATGCATCTGTCATGATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32555
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 |
---|---|---|---|---|---|
ENSDART00000033957 | Nonsense | 1563 | 2788 | 37 | 63 |
Genomic Location (Zv9):
Chromosome Zv9_scaffold3539 (position 25870)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 5883958 |
GRCz11 | 4 | 5892528 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAATGATTATACAACAGTTTTGGCCTGTTTGGTGAAAACCTTCCCGAAC[C/T]GAGCAGAGTTTCGGGATCTGGTGCAATTGACCGACTATAATGATCTGGAG
Long Flanking Sequence:
TCATTTTGTGACATTCGGAAGGCGTGGCTTTGTAGAAACCTTTGGAAAATAATGTTTTAAAGCATATTATAATATTCTAAAACATCCAGTAAATGAAATAAAATAGCGTGATGTGGCCTCTTTATGTTTCTTTTTGATTGTAGTTTTTTAGTTTCTTGCTCTTGATCTGTTTTTGAATGCTTTTTGTGTGTTTTTGTGACAGATTGGAGACATGTCTCTGGCTGACAGCGGCACCATGTGTTTGTCAGCTGTAATAACGCAGCTCTCTGAAGTGGGCTGTCCAGAGGCTCATTACAAGGAGATTGTGCAGTACATGATACTGGATGCAGTGCGAAAGGGTTTGAAGAGCAAGACTGAGGTGGAAACTAGTGCTTGCATAACACTGTATAATCTCTTCATGTGCGTATAACACCGTTATATCAACCAGGTTTTTGTTTTTACAGAGTGTACGGAATGATTATACAACAGTTTTGGCCTGTTTGGTGAAAACCTTCCCGAAC[C/T]GAGCAGAGTTTCGGGATCTGGTGCAATTGACCGACTATAATGATCTGGAGTCTGATTTCTTTGAGCATATGAAGCACATACAGGTAACGTCTGTACACTTTATTAACAGCAGAGGTCTCTAAGATGTATGAATTGACCTTCTTAGGTCTCTAGGTATATAAATGCAAAACGTGACATCAGCTCAAAGTCGGTCTGTTTTCCAGGTTTACAGAAGGGGTCGTGCCCTCAGAAAGTTTGCCCGTCAGCTGACCGAGGGCAAGATTGTGATGTCATCACGCTCCATGCAGAACTACATCATGCCCTATGCCATGATCGCTCTAGTTGATGAAAAACTGCTGAAGGTGTTACATTTTTGACCGATTTAAATTAATCATTACTCAAAACCTTCTCAGCTTTAAACTAATTGCGTTCTTTGTGTTTTCTAGTATGAACCCATGACAACAGCGGCTGTAGAAGTTGTTGGCGCCGTTTGCAGACGCTTGACCTGGTCCAAATACCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30375
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 |
---|---|---|---|---|---|
ENSDART00000033957 | Nonsense | 1891 | 2788 | 44 | 63 |
Genomic Location (Zv9):
Chromosome Zv9_scaffold3539 (position 29113)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 5887201 |
GRCz11 | 4 | 5895771 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACACTTTAGTGAAGATTTTGCAGACTCTTGGCCATCAGTACCTTCATTA[T/G]CTGCTCAGTGAGATGCAGGCGGTTTTAGTAAAGGGTTATCAGGTAAAATA
Long Flanking Sequence:
TTAAGAAATACGATATTGCAGGAATTAGACTTTGTTTTATTGCACAGTTTCCTGTAGATTACAGTGTTAGCTTTTTCTCTAATGACTCCAAAACTCCAAAAATACACAGTACATTTGTTTCTAGACTCACACTGAAGCACACAATTGTTTATTTCTGCAGGTTAAACGTGATGACGAACACAAGAGTGTGAAATCTAAGGAGGTGAAAGATGAAGAGGTGGTCAGAGTGCCTATCGCATTCGCCATGATCCAGCTCATGAAGACTCTGCCGAAGGACGTCATGGAAGCTAACTTACCTGGGTATGATTGATACCTGGGATGGAGATTTTACAGTGCAACCTCTGATCAGCAAAACATTATGCTGGGTTTGGTGTTTATATGTGCAGGATCCTGTTGAAAGTTTGTGTTCATCTGAAGAGCCGCTTCCAGGAGATTCGTGACGTTGCTCGAAACACTTTAGTGAAGATTTTGCAGACTCTTGGCCATCAGTACCTTCATTA[T/G]CTGCTCAGTGAGATGCAGGCGGTTTTAGTAAAGGGTTATCAGGTAAAATAGGATTTTTAATGTGTTTTTTAATAGCGTAATATAGACATGGACTAAACAAACTAAATCACAGATCACTGCCTCATAAATAATTTGTCCTCACAGGTCCATGTTCTGACCTTCACTGTATACCATCTGCTCTTGGTCCTGAAACCATCTTTGACCGGCGGTGATCTTGACCCGTGCATGGACATGCTCATTGCGGTAAATGCCACCAACAATACTACATTTTCAGTCAGAATTTTATGCACTTCCATTGACTAACTCTCCACACTTTTTTCTAGATCTTCAACAATGAGCTTTTCGGAGCCGTTGCAGATGAGAAGGATATTAAAGGAATTGTTTCAAAGGTGATGGAGGCCCGTCACAGCAAAAGCTCTGACTCGTATGAGTTCCTCGGACAATTCTGTGGTCAGGAGCGCGTCATTAGCCTCATCCTGCCACTCAAAGAGGTCAGTAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30376
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 |
---|---|---|---|---|---|
ENSDART00000033957 | Essential Splice Site | 1905 | 2788 | 44 | 63 |
Genomic Location (Zv9):
Chromosome Zv9_scaffold3539 (position 29156)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 5887244 |
GRCz11 | 4 | 5895814 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCATTATCTGCTCAGTGAGATGCAGGCGGTTTTAGTAAAGGGTTATCAG[G/A]TAAAATAGGATTTTTAATGTGTTTTTTAATAGCGTAATATAGACATGGAC
Long Flanking Sequence:
ACAGTTTCCTGTAGATTACAGTGTTAGCTTTTTCTCTAATGACTCCAAAACTCCAAAAATACACAGTACATTTGTTTCTAGACTCACACTGAAGCACACAATTGTTTATTTCTGCAGGTTAAACGTGATGACGAACACAAGAGTGTGAAATCTAAGGAGGTGAAAGATGAAGAGGTGGTCAGAGTGCCTATCGCATTCGCCATGATCCAGCTCATGAAGACTCTGCCGAAGGACGTCATGGAAGCTAACTTACCTGGGTATGATTGATACCTGGGATGGAGATTTTACAGTGCAACCTCTGATCAGCAAAACATTATGCTGGGTTTGGTGTTTATATGTGCAGGATCCTGTTGAAAGTTTGTGTTCATCTGAAGAGCCGCTTCCAGGAGATTCGTGACGTTGCTCGAAACACTTTAGTGAAGATTTTGCAGACTCTTGGCCATCAGTACCTTCATTATCTGCTCAGTGAGATGCAGGCGGTTTTAGTAAAGGGTTATCAG[G/A]TAAAATAGGATTTTTAATGTGTTTTTTAATAGCGTAATATAGACATGGACTAAACAAACTAAATCACAGATCACTGCCTCATAAATAATTTGTCCTCACAGGTCCATGTTCTGACCTTCACTGTATACCATCTGCTCTTGGTCCTGAAACCATCTTTGACCGGCGGTGATCTTGACCCGTGCATGGACATGCTCATTGCGGTAAATGCCACCAACAATACTACATTTTCAGTCAGAATTTTATGCACTTCCATTGACTAACTCTCCACACTTTTTTCTAGATCTTCAACAATGAGCTTTTCGGAGCCGTTGCAGATGAGAAGGATATTAAAGGAATTGTTTCAAAGGTGATGGAGGCCCGTCACAGCAAAAGCTCTGACTCGTATGAGTTCCTCGGACAATTCTGTGGTCAGGAGCGCGTCATTAGCCTCATCCTGCCACTCAAAGAGGTCAGTAACTAAAAATCATTCACAATAGTCTGATCCAAAAAGGATTTATTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44386
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 |
---|---|---|---|---|---|
ENSDART00000033957 | Nonsense | 2223 | 2788 | 51 | 63 |
Genomic Location (Zv9):
Chromosome Zv9_scaffold3539 (position 34170)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 5892258 |
GRCz11 | 4 | 5900828 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAGACTCGCAGCTGCAGGTGCTTCTGGGATACGCAGAGGAGGACATTTA[T/A]GATCACTCTCGACAAGCCACAGCATTCGGCCTCCTGAGGGTGAGACATTT
Long Flanking Sequence:
AGACCCCTCAACCCTCTTCACTTTCGCCCGTGACAACCTCCCGCTCTTCACTTTCGTCCTTCGTCCGTGACACCTCTCCGCCATTCAACACCCAAGGCATTGATAAATGCTGCAAAATTCCATTAAGTAACCCTCTGGGTTTCCCGAAATCAGAATCGAGTTGTACTCCATTGGGTCAAAAGTGACCAAAGACCACAAAGTTTTATTTATTTATTTTATTAATTTTCTTTTTAAGGAAAATCATTCAAATCTTATTCGTTTAATAATATTTTTTCTTTTTAATAAATCATAAATAGTGACTGAGGATGCACAAGGGGTTAAGAATCGTCAATGTTGTTTTTGTGATAATTTTATCACGTTCTCATTATGAAATATAAATTAGATTAATTGATGCCATGTTGTGTTTTATAGGCCATTACTGTTTTGGTGAAGAGCACTACTAAGCCTATAACAGACTCGCAGCTGCAGGTGCTTCTGGGATACGCAGAGGAGGACATTTA[T/A]GATCACTCTCGACAAGCCACAGCATTCGGCCTCCTGAGGGTGAGACATTTACGTCAAATGAGGCGTATTTTACATTATACACATGCTTTTGGTGGGATCCTTATGGTCATGGAAACCCTAATATAAAAATAAACATTGGTAAAGCCTTGCACACTTTGCTAGTTATTCTTAGTGCTATTGTTATAAACATTAGCTAATATACAATATAAACAATTATATTAGATAGATATTTAGATATATTTAGATAGATCATCTATATTCATATTTAGATCTAATCTTTATATTTAGGTAATCTTTAACTTTATTAGAAGATTGATAGATTAAAAAGTAAAAGTTTCAAACTCAGAAGTTTCTAAACATCTTAGAAATGATCTGGTCTAAATATGATTTGTTTGTCTTGGTCTTTGCAGTCGATTCTGTCCAGGAAACTGGTGGTGCCAGAGATGGAGGACGTTATGAAAAAAGTGGCCAAGTTTTCCATCGATGGGTCAAATGAACAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24760
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000033957 | Essential Splice Site | 2384 | 2788 | 55 | 63 |
Genomic Location (Zv9):
Chromosome Zv9_scaffold3539 (position 36413)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 5894501 |
GRCz11 | 4 | 5903071 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCAGAATTCCATGTTTAACCTGGTCAACAGCTGGATTTCAGGCGAGAAG[G/A]TGAGTAGATAAACCAGTATTTGTTACTTTTGTAATGTTTGTAGTTTTGGT
Long Flanking Sequence:
CTGGGGCCCCATAAATAGTGGAACTTCTCTTAATTTTAATTTAATTTTACATTTAGAAGTTAATGCTTCCACTTGTAATTATTTTTTAACATGAAGTTTATTTACAAAAAAAGCTAAACAAAACAAAACAACAACTAAAGAATATATATGAATAAACAAATCTACAGAAAAAAATATCTATAGTGAAAGAGAGTGTTTTGATTTTCAATGCTAGGGCCCCATACATGAAATTGCTTAAGGCCTCCAAATCACTAAGTCCGCCCCTGTGTGTTAATTATATTGAAAGATTATAGTTTATTTTGTTGTTATGTTCACAGGCTCTCTTGCATGAGCACTGCGGTTTGTTCTTTGTGCCGTTGTCGTTGGCCGTGTTAAACGATGATTCTGCAACCTGTAAGAAAATGGCATCTCTCTCCATCAAGTCTCTTCTGAATCAGCTGGATTTGCAGCATCAGAATTCCATGTTTAACCTGGTCAACAGCTGGATTTCAGGCGAGAAG[G/A]TGAGTAGATAAACCAGTATTTGTTACTTTTGTAATGTTTGTAGTTTTGGTGTAATNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNGAATTCCATGTTTAACCTGGTCAACAGCTGGATTTCAGGCGAGAAGGTGAGTAGATAAACCAGTATTTGTTACTTTTGTAATGTTTGTAGTTTTGGTGTAATGGTTTGTGATTTTGCAGACGGCTCTGCGCAGACTGGGAGTTCAGATTTGTGGGCTGTTTGTGGAAGTTGAAGGGGAAAAGTTCAGCAGGAGACTGGACGTCCTGATTCCTCTCATCGAGAAAGAGATCCACGCTGACAACTTTGAGGATGTGAGTGCAGATTTGAGCATTTTCTTTATTGTTATTTTTAATTTTGAGACATTTTCCTTAAAGAGAACAGGGTTACCATAAACTGGAACATCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30377
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 |
---|---|---|---|---|---|
ENSDART00000033957 | Nonsense | 2545 | 2788 | 59 | 63 |
Genomic Location (Zv9):
Chromosome Zv9_scaffold3539 (position 40042)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 5897928 |
GRCz11 | 4 | 5906498 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTTTCTTTCTGCTCTGTCAGATGAGAGAGCTGGTTCTGGCCTTCTGTTA[T/A]CAACTGCAGTCCAAGTTCTTGGATATTTCTGCAGGGGAGCAGGTAGGAAA
Long Flanking Sequence:
AAACATGTTTAAAAAAGTGCTGGATGAGTTGAATTTGTATCTTTAGGTGAACTATTTCTTTAATGAAGGGACATTATTGTGATGTATGCATTGACTTCAATAGTAGGAGTAAAATACTATAGAAGTCAATGGCTGTTGGCTTCTAACATTGTTTATTTAATGAAGTGAAATCATTGCGTCTCTTTATGCAGGTCATATTGATTCTCATCTGCGCTATCCTCATTCTTGGGTTTGGCTGACCGCGTCTCAGATCTTTGGTCTGCTGTTTGCTGCTCACAAACCAGAGGATCTCTTGGCTTTATGGGGCTCTATGGAGAACACAGATAAAAGCACACCGCCTGTGGCCACTGCTTTCCTCACTGACAACCTGTATAAGAAGGCAAGAGCCTGAAAGAAACTGTATTTAAAGCATTGGTTATAGAAAGATTGAGTAAAGTAGTGAATGTGACTGTTTTCTTTCTGCTCTGTCAGATGAGAGAGCTGGTTCTGGCCTTCTGTTA[T/A]CAACTGCAGTCCAAGTTCTTGGATATTTCTGCAGGGGAGCAGGTAGGAAATAATGAAAAATTATTATTCATATTATTATTATGATAAATTCATATTATTATGATGATAAATATCTGATTGAAAATAAGTAGTTACTATTTTATTGTTTAATAGAATTTTTTTTTGATCAGAAATGTAGTAGTTGTAATAATAATAATAACAATGATTAAATATGTAATTAAATTTTAACAATAAATGCATTTGAAATCATATTTCATGTTTAAATATTTTTTGTGCATTGTTATATATAAAAATGATTTTGTCAATTGTTTTGTTAATAAAATATTTAATCAAATTATTAAATAAAAAAAACATTTTCATATAATGTTCATATAATTTGACCTTTTCCATTGTTTTTAGTTACTTTCTATGTTTTTATGGAGTTTTCAATATGATTTTTGGAAATTGTAAATTAAGTACCTAATATTGTACTCCTGTGATTAAAATGTCTAATCCCTGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24761
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 |
---|---|---|---|---|---|
ENSDART00000033957 | Nonsense | 2577 | 2788 | 60 | 63 |
Genomic Location (Zv9):
Chromosome Zv9_scaffold3539 (position 40678)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 5898564 |
GRCz11 | 4 | 5907134 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGTGAAGAACTTGCTCTATGTGGCCAAAGTGATCTACCTGATCTCACCA[G/T]AGTCTGATAGCGTAAATCCACCTGAAGAACAAGAGAATATAGAGGAGGAA
Long Flanking Sequence:
TATTTTATTGTTTAATAGAATTTTTTTTTGATCAGAAATGTAGTAGTTGTAATAATAATAATAACAATGATTAAATATGTAATTAAATTTTAACAATAAATGCATTTGAAATCATATTTCATGTTTAAATATTTTTTGTGCATTGTTATATATAAAAATGATTTTGTCAATTGTTTTGTTAATAAAATATTTAATCAAATTATTAAATAAAAAAAACATTTTCATATAATGTTCATATAATTTGACCTTTTCCATTGTTTTTAGTTACTTTCTATGTTTTTATGGAGTTTTCAATATGATTTTTGGAAATTGTAAATTAAGTACCTAATATTGTACTCCTGTGATTAAAATGTCTAATCCCTGGTTTCATATTAACATTTTTTAAATAATTATAAATATTCATATTATTCTTGCAGTATGATTTTAATTGTGATTTAATCTTTTATCAGGTGGTGAAGAACTTGCTCTATGTGGCCAAAGTGATCTACCTGATCTCACCA[G/T]AGTCTGATAGCGTAAATCCACCTGAAGAACAAGAGAATATAGAGGAGGAAACGGCAGAAAACACTGAGACCAATGGAGGAGAACAGGAGCAGAAGCTCGAGGAGCAACAGAACGACAACAAACCTCCGTCTCTCCTCTGGGTGATGAAGAAGCTTTCATTACTGGCCAAAAGAGAAGCGGCGAACACACCCAAAGTGCCACTCAAGGTGGACATTAAGCCTGTCTTTCTGCTTAAATATCTTGAAAGGTATTTGTGTTTTGCTGATGTAAACCCACCTGTCTGTTGTTTTTGTAGAGAACTTGTGTTTTTAAGTTCTTGGGAGCCATAGCGGTGGATCTTGGAAAAGATCGTCTTGGACCATATCTCACCACAATCATCGCTCCTCTTTATAGAGAACTGGACAGCACATATGCAGACCAAGGTCAGTTCATAAAGCAGAAACAAGCGAACAAAAACTCAATTATTTTAGGAAACTGTTCATAACAGTGGAACTTTGTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24762
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 |
---|---|---|---|---|---|
ENSDART00000033957 | Nonsense | 2612 | 2788 | 60 | 63 |
Genomic Location (Zv9):
Chromosome Zv9_scaffold3539 (position 40783)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 5898669 |
GRCz11 | 4 | 5907239 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGAAAACACTGAGACCAATGGAGGAGAACAGGAGCAGAAGCTCGAGGAG[C/T]AACAGAACGACAACAAACCTCCGTCTCTCCTCTGGGTGATGAAGAAGCTT
Long Flanking Sequence:
TTGAAATCATATTTCATGTTTAAATATTTTTTGTGCATTGTTATATATAAAAATGATTTTGTCAATTGTTTTGTTAATAAAATATTTAATCAAATTATTAAATAAAAAAAACATTTTCATATAATGTTCATATAATTTGACCTTTTCCATTGTTTTTAGTTACTTTCTATGTTTTTATGGAGTTTTCAATATGATTTTTGGAAATTGTAAATTAAGTACCTAATATTGTACTCCTGTGATTAAAATGTCTAATCCCTGGTTTCATATTAACATTTTTTAAATAATTATAAATATTCATATTATTCTTGCAGTATGATTTTAATTGTGATTTAATCTTTTATCAGGTGGTGAAGAACTTGCTCTATGTGGCCAAAGTGATCTACCTGATCTCACCAGAGTCTGATAGCGTAAATCCACCTGAAGAACAAGAGAATATAGAGGAGGAAACGGCAGAAAACACTGAGACCAATGGAGGAGAACAGGAGCAGAAGCTCGAGGAG[C/T]AACAGAACGACAACAAACCTCCGTCTCTCCTCTGGGTGATGAAGAAGCTTTCATTACTGGCCAAAAGAGAAGCGGCGAACACACCCAAAGTGCCACTCAAGGTGGACATTAAGCCTGTCTTTCTGCTTAAATATCTTGAAAGGTATTTGTGTTTTGCTGATGTAAACCCACCTGTCTGTTGTTTTTGTAGAGAACTTGTGTTTTTAAGTTCTTGGGAGCCATAGCGGTGGATCTTGGAAAAGATCGTCTTGGACCATATCTCACCACAATCATCGCTCCTCTTTATAGAGAACTGGACAGCACATATGCAGACCAAGGTCAGTTCATAAAGCAGAAACAAGCGAACAAAAACTCAATTATTTTAGGAAACTGTTCATAACAGTGGAACTTTGTTTTTTCATGGCATCATTTATCTTTTATTACTTTCTTGGAGTGGTCAACATCTCGCAAATTCTGACATTTACTGTCAGGCTTCATCTAATTTGGCTTGCAACTTTTAT
Associated Phenotype:
Not determined