ZMP
usp19
Ensembl ID:
ZFIN ID:
Description:
Ubiquitin carboxyl-terminal hydrolase [Source:UniProtKB/TrEMBL;Acc:B7ZDA8]
Human Orthologue:
USP19
Human Description:
ubiquitin specific peptidase 19 [Source:HGNC Symbol;Acc:12617]
Mouse Orthologue:
Usp19
Mouse Description:
ubiquitin specific peptidase 19 Gene [Source:MGI Symbol;Acc:MGI:1918722]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa24302 | Nonsense | Available for shipment | Available now |
sa13973 | Essential Splice Site | Available for shipment | Available now |
sa17379 | Nonsense | Available for shipment | Available now |
sa43956 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa39403 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa37674 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa12637 | Nonsense | Available for shipment | Available now |
sa3231 | Nonsense | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa24302
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 |
---|---|---|---|---|---|
ENSDART00000112840 | Nonsense | 15 | 1436 | 1 | 25 |
ENSDART00000132025 | None | None | 227 | None | 5 |
ENSDART00000147778 | Nonsense | 15 | 1478 | 2 | 26 |
Genomic Location (Zv9):
Chromosome 23 (position 20464182)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 20249289 |
GRCz11 | 23 | 20175632 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCTGAAAATGGCCAGCAGCAGCACAGGATCCAGCGAATCAGGCCGCAGG[C/T]GAGGTCAGAGGGGACCGGATGACACGGTCAGCACCAGCAAGAAGAAGCAG
Long Flanking Sequence:
TGTCTGAACTGTCCAATCGTCACAAAATAATGACATAATCCAGGTTTTTGGATTGTACAGTGTATGAATACCCACGAGTAATTGTTAACCCTGGGTAAATTATGAACATTGGGCAAGGGACCAAGGATTTATTATTTCAAGTGTGATTTTATGTGATATCCTTCAACTTTGTCTGCCCTAACATTCGATCAGAAATTAAAAGTTGTTTCTTGTATAATTCCATCATTTTACTCATGTGTACTGCCGGTAAAATGGAGTCTGTTTGTATTACATCATCGCTGTTGCTTTTGTTTACAGTCTCCTGATTCTCTTCTGGGAGTGCTCTCACTTGAAACGCCGCCAAGATAGCTGGACCGGGCAGGAAACGGCACAGCTCAGATCCAGACCCCAGTGGAAGCGGCTCCGGCAGCGGGAGCGAGGTAGGAGACGGCCGAACCATCAGCGGCAAGTGGCTGAAAATGGCCAGCAGCAGCACAGGATCCAGCGAATCAGGCCGCAGG[C/T]GAGGTCAGAGGGGACCGGATGACACGGTCAGCACCAGCAAGAAGAAGCAGAAGGACAGAGCCAACCAGGAGAGCAAAGAGGCCAAACGGGTGGCTACCAGCACAGAGACTAAGAAAGGTGAGGCGAGGACAATGTAGTTTATAAACCCCCATAAACCAGGTCTGAATTACTTTATTTCACTCAGGTCTTTTACGCAAGTTCATTTGAATGCTTTTCTTTGTGATCGTGCTTTCACTTTTGTCTCTCGCCAAGTGTTAATCAGTCTTGTAAATCAAGATGTTGAGATTTATGGTAAATGGTTTACTACAGTGATGTCTAATGTAATATGAACTGATGGGAAGAGTCTGTGGTGCAGTGTCCTTTTGACCGTAATGCAGTTTGGCCCATAACTGGTGGTTAAAGGCATTAAAAGAGATTTTAGAGTCTTTGGGATAATTTCCTATTTGTTATTTGCTATAGTAAATAGTGAACTAGAAAATTAACAGACGTTAACTGTGTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13973
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:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112840 | Essential Splice Site | 414 | 1436 | 5 | 25 |
ENSDART00000132025 | None | None | 227 | None | 5 |
ENSDART00000147778 | Essential Splice Site | 414 | 1478 | 6 | 26 |
Genomic Location (Zv9):
Chromosome 23 (position 20456416)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 20241523 |
GRCz11 | 23 | 20167866 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGTCCAAAGAGGAGCCACAAGGAGCAWGCCAAGAGGAGGATACGGAAGG[T/A]CAGTTAAAGGCATAGTTCATCCCAAAAYGACCAGCTCCCACCCRAATGTC
Long Flanking Sequence:
CATCAAGCAATGCAAAAGACAACAGGGCTCAGATGCAGGGCAAACCTCAAGGATGCCAGGCATTGCAAAAAGAAAAAGGGATTGACAGGAAGCCAAAGAGCAATGCTCAGGTAAGCTAATAATAGTAATCTGCAAATAAAATCATGAAAAAATTCTCTGAAATCCTGTTTGTCTTGGTGTTGTTTATAGGTTGGATCAGGGGAAAGCAAGAGCGTCTCTGTGTGTGAGCCGCAGGTACCGCAAAAAGACCATTCTACTCCTGTAAAAACATGCACTGATAAAATAGCGTCTGATGAGCCAGAAAACAGAAAGGAGGAAACGAAGCCACAGGCTGAAGGCCACATCCCTAAAATGCTTCCCTCTCATGACTTGGGATCTGGAGAGCCTGCATCAACAGACTCCAAAAGAGAGGAGTCTCCACAAAAGAGCCACACAGAGGAGAAGAGGGACAAGTCCAAAGAGGAGCCACAAGGAGCAAGCCAAGAGGAGGATACGGAAGG[T/A]CAGTTAAAGGCATAGTTCATCCCAAAACGACCAGCTCCCACCCAAATGTCATTCCAAACTCATAAGTAGGCCTACATGGAATCTGCGCATGCAGAAATCTGCCCATCATTGAGTCTATTTATTTACATGTGTAAATGTATATTTATTAAGTTAATTATTTCCATAATCTTGACTAATACGAAAATGTTAATATGATTTGTTTACAATTCAGTTTGTAAAGTAATATTTTCTGTCTTTTAGTTGATATATTATATGAGAGACTTGCTTTGTTTCCCAAATAAGTGGACACAAGTGGATTTGTTCTGTAAACATTAAATAAAAGTTAGAAAGGTATTACTTTTTATATTATATAGTAAGTTTTTAGTTACACTCCGTAAATCTATGCATGCATACATTCACAGTTTTTTTTTCAGTAAATTCTGTGCAGAAATAGGAACAAAATGTCTACAGATTCTGTCTGGCCCTAATAAAAATATTAGTGATCCTCATTAGTTTTTGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17379
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112840 | Nonsense | 647 | 1436 | 10 | 25 |
ENSDART00000132025 | None | None | 227 | None | 5 |
ENSDART00000147778 | Nonsense | 647 | 1478 | 11 | 26 |
Genomic Location (Zv9):
Chromosome 23 (position 20450985)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 20236092 |
GRCz11 | 23 | 20162435 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAAGTATGTCACCCTGGCTTCACTGGACTGGTCAATCTGGGAAACACTTG[C/A]TTTATGAACAGTGTGATCCAGTCCCTCTCCAACACACGGGAGCTCAGGGA
Long Flanking Sequence:
TAGATGTATGCAAAACTATATAGGAAGTGTCTGGTGCATATTGAGAAGAAAGAGTGTTTCCCACAGGTGGTTTGTCCAGCCCACTCACCTGCGTGAATAAATAGCCATTTATGACCACTGTTTAGTCATATCACATAATAAAGCAAATCTTTACTACAATCTCTGGACTTGCTACAGATAGCAACTGGTGTCTTCTGAGATTAGACCCGAGTATAAACATTACATTCATGATTTTTTTAGTAGTATCTCAGCACAATGTGAGCGTAAATGTACAGTTTACTGTTCTCTTATGGCATCTGATAGAGCATTTGCACCCAGAAACTGAAGTGAATAGGTTCTTATTAGGCTTCCTATGCCAACTGTCCACAGCCCAAACCCACCTGCATGGTGCAGCCCATGACCCACACTCCTCCGGTAGGCAATGAGAGATCAGAAGAGGTGGAGGAGAAAAAAGTATGTCACCCTGGCTTCACTGGACTGGTCAATCTGGGAAACACTTG[C/A]TTTATGAACAGTGTGATCCAGTCCCTCTCCAACACACGGGAGCTCAGGGATTATTTCCATGGTCAGTTACATTTTCTACAGAATATTACATTTTTTCATATGCCTATGTGTCTTAAGTTTATTAAGACGTGTGTGTTTTCAGATCGAGGTTTTGAGTCAGAGATTAATTGTAATAACCCATTGGGCACGGGTGGACGGCTGGCCATTGGCTTTGCTGTTCTGCTACGGGCGCTGTGGAAGGGCACTCATCATGCTTTTCAACCCTCCAAATTAAAGGTATTTTTAGATTCTTCTCCTATACTGCATCTTTAAGTTATGTTAATTACACATTATAAATGGTTGTTTCTTCATTTCTCTTTCTAGGCTATCGTTGCCAGTAAAGCCAGTCAGTTTACAGGTTATGCGCAGCATGATGCTCAGGAGTTTATGGCTTTTTTGCTGGATGGTCTTCATGAAGACCTGAACCGCATCCAAAACAAACCATACACCGAGACTGTGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43956
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 |
---|---|---|---|---|---|
ENSDART00000112840 | Nonsense | 677 | 1436 | 11 | 25 |
ENSDART00000132025 | None | None | 227 | None | 5 |
ENSDART00000147778 | Nonsense | 677 | 1478 | 12 | 26 |
Genomic Location (Zv9):
Chromosome 23 (position 20450814)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 20235921 |
GRCz11 | 23 | 20162264 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTAAGACGTGTGTGTTTTCAGATCGAGGTTTTGAGTCAGAGATTAATTG[T/A]AATAACCCATTGGGCACGGGTGGACGGCTGGCCATTGGCTTTGCTGTTCT
Long Flanking Sequence:
CTACAGATAGCAACTGGTGTCTTCTGAGATTAGACCCGAGTATAAACATTACATTCATGATTTTTTTAGTAGTATCTCAGCACAATGTGAGCGTAAATGTACAGTTTACTGTTCTCTTATGGCATCTGATAGAGCATTTGCACCCAGAAACTGAAGTGAATAGGTTCTTATTAGGCTTCCTATGCCAACTGTCCACAGCCCAAACCCACCTGCATGGTGCAGCCCATGACCCACACTCCTCCGGTAGGCAATGAGAGATCAGAAGAGGTGGAGGAGAAAAAAGTATGTCACCCTGGCTTCACTGGACTGGTCAATCTGGGAAACACTTGCTTTATGAACAGTGTGATCCAGTCCCTCTCCAACACACGGGAGCTCAGGGATTATTTCCATGGTCAGTTACATTTTCTACAGAATATTACATTTTTTCATATGCCTATGTGTCTTAAGTTTATTAAGACGTGTGTGTTTTCAGATCGAGGTTTTGAGTCAGAGATTAATTG[T/A]AATAACCCATTGGGCACGGGTGGACGGCTGGCCATTGGCTTTGCTGTTCTGCTACGGGCGCTGTGGAAGGGCACTCATCATGCTTTTCAACCCTCCAAATTAAAGGTATTTTTAGATTCTTCTCCTATACTGCATCTTTAAGTTATGTTAATTACACATTATAAATGGTTGTTTCTTCATTTCTCTTTCTAGGCTATCGTTGCCAGTAAAGCCAGTCAGTTTACAGGTTATGCGCAGCATGATGCTCAGGAGTTTATGGCTTTTTTGCTGGATGGTCTTCATGAAGACCTGAACCGCATCCAAAACAAACCATACACCGAGACTGTGGACTCAGACGGCCGTCAGGATGAAGTGAGCTTTTAAAAACAATTCTACATAACATTACATAAGCAAAAAAATATGTAAATCACTTGATTTTTTTTAATTGTATACATTTTTTGGTAACACTTATACAATTGGGGAGTAAGTTTATATTAGTTAATGTTAGTTAATGTATTTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39403
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112840 | Nonsense | 791 | 1436 | 13 | 25 |
ENSDART00000132025 | None | None | 227 | None | 5 |
ENSDART00000147778 | Nonsense | 791 | 1478 | 14 | 26 |
Genomic Location (Zv9):
Chromosome 23 (position 20449865)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 20234972 |
GRCz11 | 23 | 20161315 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATAAAATGAGAAACGATTCCTTCATTGTTGACCTCTTTCAAGGCCAGTA[C/A]AAGTCAAAGCTGGTGTGTCCAATGTGCTCCAAGGTATTTCATGTCAAAAT
Long Flanking Sequence:
TATACAATTGGGGAGTAAGTTTATATTAGTTAATGTTAGTTAATGTATTTATTAAAATAAACAAACGATGAACAATGACATCTTTGTTCATGTTAGCTGATAAAGTTGTTCATTGTTAGTTCATGTTAACTTATTGCATTAACTAATGTTAAAAAGCTTGAATATGGATAGTAAATTTTGAACTATGATTAATAAATCCTGTACAAGTATTGTTCATTATTTTTGATATTAATAAATGCATTAACATTATCCAAGGAAACCCTATTGTAAAGTGAATAATTAAATATTTTGCATTCAGTTACAAACAACTATGATATTCTTTAATTTTTTTATTATTATTAAGCAAAATCAGCTCTATGTTGTGAATTCCTTTTTTCATGATAATAAATCTGCTGAAAGTTGTTTTTGTTTGTGTTTTGGTAGGTTGTTGCAGAAGAGGCATGGCAGAGGCATAAAATGAGAAACGATTCCTTCATTGTTGACCTCTTTCAAGGCCAGTA[C/A]AAGTCAAAGCTGGTGTGTCCAATGTGCTCCAAGGTATTTCATGTCAAAATGAGCTACAGTATGATTCTAATTCAGATTCCCATTCAGATATTTGTAGTCTTTTGCGCTCATTGAGGCTACTATGATTTTAAAAAATGCTTATGAATGTTGCAGAAATGCTCATGAATGTTGCAACAATTTTGTTGAATAATGTTGATATTTTTGAAAGAATTATGCATTTCCTTTCAGTATGATTAATGGTAAAGAAAACAGTTAATTTGAAATGGAAATGTTTTGGCAAAATGTAAAAATGTCTTCATTAAAGAATAAAATCAACAATAAAATATTTCTGTCAGAAAGTATATATTAAGCAATGACCCCAAACTTTAAAACAGTTCTAATTTAAAAAGTTTTAAAAACTGTCTACACTTTCCATGCTTGGACCCACTTTAAATCATTTACTTTGTAAAAGAATCATTCCTTTTTTAAAATGTTTGGGAGATAATTACGATTTTCACTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37674
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112840 | Essential Splice Site | 960 | 1436 | 17 | 25 |
ENSDART00000132025 | None | None | 227 | None | 5 |
ENSDART00000147778 | Essential Splice Site | 953 | 1478 | 18 | 26 |
Genomic Location (Zv9):
Chromosome 23 (position 20447446)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 20232553 |
GRCz11 | 23 | 20158896 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAAGCTGAAGCGCTGCACACGCTGTTATCGTGTCGGCTACTGCAATCAG[T/C]GAGTTGTGTGTTGTTCTGGCTTTGACATCACACATAAGATTTAGAGATTT
Long Flanking Sequence:
CTATCCCTTTAAGTATTGCCTTTAGAATTAGAGTATGATCAAATTTTTTTGGCAGCCATATTTACAGTGCTTTAGTTGTGTGTCATTGAAAAGTTCTATACTCTCTAATTTATGTTTTGTTGTTTTTTCCCCTCAGGTTGTGAAGGGCAGGTTCCACAGAATCTTCTCACCGTCTCAATCTTTAGACACGGTCTCGTCCAGTGACCTGCTCTTCTGCTTTGAGATGCTGTCAAAAGATCTCATCAAAGAGAGAGTGGTGTTGCTGAAGGTCCAGCAGGTACGCCATTTACACCGCTCTTACTTTCTTCCCTTAACTATTGCCGATTTTTGTTAGCATTTGCCTTTTTTCTTGCTATAATCATGTGTTTTTTTATCTTCAGAGACCTCAGATTCCTAGCATACCAATCACAAAGTGCGCTGGTTGTCTGAAGCCTCCTGCCTCTGACGATGAGAAGCTGAAGCGCTGCACACGCTGTTATCGTGTCGGCTACTGCAATCAG[T/C]GAGTTGTGTGTTGTTCTGGCTTTGACATCACACATAAGATTTAGAGATTTTGCCTTTGGCGTAGTTGGTAGTAAGAATTTTTTCTGATTACAGGACCTGCCAGAAGAACCACTGGCCTTCTCACAAGACTATGTGTCGGTCTAATGTGGAAAACATTGGACAGCCATTTTTAATCAGCGTGCCTGAGTCTAGACTTTCTTACACTCGCCTCACACAGCTTCTAGAAGGCTACTCTAGGTATAATTACAGCTATATTCAGATTTGTTTACCTATCTATGTAATTCAGTCAGGATTAGATGAAGATATAATTAAAACACTGATAAAATTTTAGTATTTATTTATTTATTGCTTTATCTGTCAGTCTATTTGTATGTCATTTATTTATTTTTTAAATAAATAGATTGTAAGGTTTTATATACATTTTATACATTGTATGCATTTTTGTGCCAATTTTGTGTAGGTTTTTTATTTAGAAAGCATATATTTTTATTATTATCCTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12637
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112840 | Nonsense | 1178 | 1436 | 21 | 25 |
ENSDART00000132025 | None | None | 227 | None | 5 |
ENSDART00000147778 | Nonsense | 1171 | 1478 | 22 | 26 |
Genomic Location (Zv9):
Chromosome 23 (position 20443066)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 20228173 |
GRCz11 | 23 | 20154516 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGTGCACACTAGAGCTGGTGTGGAAGAACAACGAGCGGCAGAAGGAATA[T/A]GTGCTGGTGCGCTCTAAAGATCTGGAGTTYGATGAGGACCCRGGCTCTGC
Long Flanking Sequence:
TAACCTCAAAATTCTGAAGCAAAAAGCAGATTTTACTCTCTACAAGCAGGTTGAACTTCTCAATAGCTATAAAATAATGTTTCCAGGGTTACTTCCCCTAAATAAAGCAGTGCTGCACTTTCAAACAGAACTTTAATATGTATCATTCAGGGATGAGAAGAAAAGAAAATACCACATTAGCTCTTCTGAAGGAAGTCATTTTCTTGAGGAATTTGTTCATAAAAACTGCTATGCCAGTTGTATTGTGATTTGTTTGGCATTTATTGTCATTTGAACCACCACATATTTTAAACTATTTTTAAGTTTTAGGCATCAAATTCAATCATTTCTGCTCCAAAGTTTGTGTTCTGATTCTGCCTTATTGGCTCTGGGTTTCAGTACCAAACCTTATTGTGTGTTTTTACCATCTTTTTGTCTCCTGCAGGTGACGCGGTACTGGAGCTGCCTGATGAGTGCACACTAGAGCTGGTGTGGAAGAACAACGAGCGGCAGAAGGAATA[T/A]GTGCTGGTGCGCTCTAAAGATCTGGAGTTTGATGAGGACCCGGGCTCTGCTACCGAGACCTCCAGGGCAGGACACTTCACCTTAGAGCAGTGCCTCAACCTCTTTACCAAACCTGAGGTCCTAGCCCCTGAGGAGGCATGGTATGAACACGCACTCAGAGTGCCCATAGAAAGTGTTCAAATAAAACTGTATGTGTGGTCATATTTATTTTTCTTATTCAGGTACTGTCCTAAGTGTCAGCAGCACAGAGAGGCCTCTAAACAGCTCCTACTTTGGCGTCTTCCGAATGTACTCATCATCCAGCTCAAGCGCTTCTCATTTAGGAGTTTCATATGGAGGGACAAGATTAATGACATGGTCGATTTTCCAGTCAGGTATACTGAAAGTTACTCAAAGTTTCGTAGACTTTCACTTGCACTGGTGTTTGAATGCTTAAATTTTCCCTTTCACAATTAAGTATCTACTATTCACGACAGAAATAACATTGTACTTAGAAAAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa3231
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 |
---|---|---|---|---|---|
ENSDART00000112840 | Nonsense | 1409 | 1436 | 25 | 25 |
ENSDART00000132025 | Nonsense | 200 | 227 | 5 | 5 |
ENSDART00000147778 | None | None | 1478 | None | 26 |
Genomic Location (Zv9):
Chromosome 23 (position 20434744)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 20219851 |
GRCz11 | 23 | 20146194 |
KASP Assay ID:
554-3198.1 (used for ordering genotyping assays)
KASP Sequence:
TAGCCAGACACTGTTTGGGACAGACCTGGATCCTGACGGGCCCCCTCAGT[T/A]GAGCACGGAAGTGACCTCAGACATGTTTGCACACTCTGGAGAATGTGCCG
Long Flanking Sequence:
GGGCTCAATACTGTACTTCTGTTTTCCCTCTACTATGCACCATTGATTCAAAGCCTGATTGCACATGTTGTACATTGACATGAGATCCTTATATTGTAATATGAGCGCTACTCTAGTTAATGGATATGTGGCATTTTCTACAGTCTCAGGGATGCTGGTGGCCTATTCATTGTTTGTGTTTCCATCCACACTAAAAAAGCCTAACAGACATTTGGCTTCTGTGAATGCCTCAACTCTGGACACCATGACTGAAAAACAACACCATCAGATATAATTGTACCTCATCACAGATTGTAATTACGAATGGTCCTGGATAAAATGATTAAGATCTGTTTTTTGTTTTGTTTTTTCTCATCATAATGGTCTTATTTGCAGTTGGCGTTCATGTACTCCGTTCCGAAGGTGCATGACGTTTCTCTCTTTATAACGGTGGTTTATTTTACAGGCTTCTAGCCAGACACTGTTTGGGACAGACCTGGATCCTGACGGGCCCCCTCAGT[T/A]GAGCACGGAAGTGACCTCAGACATGTTTGCACACTCTGGAGAATGTGCCGCCCCGTCCTACAGCAGCATGGAGGAGGTGGATTGAAACTTGACCCGGTCAGGGAGACTTGCTTTCTCCAAACAAAACAACAAACATTAATTGACGTTAATGCTCACAAGTGGATCTAGCATGGCAAAGGTGCTCTATTTCCTTTTTTTATTGTTATTATTATTATTTACATTTGCAATGTGGACACAAGAGGCTGGGTGTCCATTTCCAATACAAAGACTGCTTGTTTTGGAAACAGCCTGAATGTTACGATACAACAAGGCGATGATGCTTAAGGACTAATCACATATTCACAAATATTTCTGGAAAGTGCACAAATTGAAATACACCATCGGTGGTAAGAGGAAGCGCACAGATCTGAAAGGTTTTTTATGACTATGAAAACATTTTAACTCCTAGGAATTATGCCGTTCACAGTTTCACATTAGGTTTCTACTAAAATGTTTCTCTT
Associated Phenotype:
Not determined