ZMP
si:ch211-257m21.2
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate ubiquitin specific protease [Source:UniProtKB/TrEMBL;Acc:A2BIA9]
Human Orthologue:
USP24
Human Description:
ubiquitin specific peptidase 24 [Source:HGNC Symbol;Acc:12623]
Mouse Orthologue:
Usp24
Mouse Description:
ubiquitin specific peptidase 24 Gene [Source:MGI Symbol;Acc:MGI:1919936]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa36972 | Essential Splice Site | Available for shipment | Available now |
sa11303 | Nonsense | Available for shipment | Available now |
sa6615 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa43384 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa15755 | Nonsense | Available for shipment | Available now |
sa43383 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa36972
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 |
---|---|---|---|---|---|
ENSDART00000083890 | Essential Splice Site | 624 | 2589 | 16 | 66 |
ENSDART00000144729 | None | None | 292 | None | 7 |
ENSDART00000146135 | None | None | 63 | None | 2 |
Genomic Location (Zv9):
Chromosome 20 (position 7692869)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 7527274 |
GRCz11 | 20 | 7515013 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACGAAATCACACGGTCTTTTATCAAACAAACCTACCAGAAACAGGACAAG[G/A]TAAAGCCACACAGTCTTCGAAAATAACCATCCTGCCTGTTCCATAGTACA
Long Flanking Sequence:
TTTTGATGGTCCATTTTATCGTTTAATTGATTTCGTTTTTGTTGTTGTTTTGGATGCCTTTTATTTTGGTTTGGTTCAGTTTTTAGTTTTCATTTGAAGTACTTTTCATCGTTTTTTCGAGTTGTTTGTACTTTTCTTTGTTGGGCTGACTTAGTGTTGACACCTTCCGGTAAAAATAAGTGCTTGTGCATACAATGGGCAAACAATTATAAGCATCAAGCACAGTACAAACTGCTTTGATAACACAATTTGTATTTGTATTTGTACACGTAAAAAACCCAAATGTACTTAGGGCTTTACACATCATTGACCCAAATGCAGATTCCATTATTCCATGAATGCTCTATGTGTTGTTGTATTTATATATGTGTGTGTTTGTGTTTGTATTGTAGTCTTCTCAGCAGACTAACCCTCAGACAGTGTGGGTTGTGCCAGCTTTACGGCAGCTTCACGAAATCACACGGTCTTTTATCAAACAAACCTACCAGAAACAGGACAAG[G/A]TAAAGCCACACAGTCTTCGAAAATAACCATCCTGCCTGTTCCATAGTACACTACAAAGCTCATTTTTCATGCTGTAAGTGACGATTGATTGTACATTGTGTTGTTTCCTCTGTCAGAGTATAATTCAGGACCTAAAGAAGAATTTTGAGATTGTGAAGCTGATCACAGGCTCCCTGGTGTCCTGTCATCGATTGGCCGTGTCTGTCGCTGGATCCAATGGTCTTTCCGGGTCCACACTGGTTGATGGACGGTATTCCTATCAGGAGGTACACTTGATGATCATTAGTTATCATTTGTACAATCGAAAATTTATTTTGACAGTAATGATTACTAAAGTGTTAAAAAGCTAAATTAATAATAAATTATTGAATATTATTTATTATTATTTATAATTATTGAAAATAACAGGATCTTGATGGTTTATTTTGGGTATGTTGTTTATATGAAGAAATCTGTTTTACAAGTTAAACAAAAATTTTAATAAACAATAATCGCAAAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11303
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 |
---|---|---|---|---|---|
ENSDART00000083890 | Nonsense | 672 | 2589 | 17 | 66 |
ENSDART00000144729 | None | None | 292 | None | 7 |
ENSDART00000146135 | None | None | 63 | None | 2 |
Genomic Location (Zv9):
Chromosome 20 (position 7692609)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 7527014 |
GRCz11 | 20 | 7514753 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGATCCAATGGTCTTTCYGGGWCCACACTGGTTGATGGACGGTATTCCTA[T/A]CAGGAGGTACACTTGATGATCATTAGTTATCATTTGTACAATYGAAWATT
Long Flanking Sequence:
TTTGTACACGTAAAAAACCCAAATGTACTTAGGGCTTTACACATCATTGACCCAAATGCAGATTCCATTATTCCATGAATGCTCTATGTGTTGTTGTATTTATATATGTGTGTGTTTGTGTTTGTATTGTAGTCTTCTCAGCAGACTAACCCTCAGACAGTGTGGGTTGTGCCAGCTTTACGGCAGCTTCACGAAATCACACGGTCTTTTATCAAACAAACCTACCAGAAACAGGACAAGGTAAAGCCACACAGTCTTCGAAAATAACCATCCTGCCTGTTCCATAGTACACTACAAAGCTCATTTTTCATGCTGTAAGTGACGATTGATTGTACATTGTGTTGTTTCCTCTGTCAGAGTATAATTCAGGACCTAAAGAAGAATTTTGAGATTGTGAAGCTGATCACAGGCTCCCTGGTGTCCTGTCATCGATTGGCCGTGTCTGTCGCTGGATCCAATGGTCTTTCCGGGTCCACACTGGTTGATGGACGGTATTCCTA[T/A]CAGGAGGTACACTTGATGATCATTAGTTATCATTTGTACAATCGAAAATTTATTTTGACAGTAATGATTACTAAAGTGTTAAAAAGCTAAATTAATAATAAATTATTGAATATTATTTATTATTATTTATAATTATTGAAAATAACAGGATCTTGATGGTTTATTTTGGGTATGTTGTTTATATGAAGAAATCTGTTTTACAAGTTAAACAAAAATTTTAATAAACAATAATCGCAAAACAAGTGTGATTAAATCGTTATTTTTATATAATATTTTTATATAATATAAATAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACTATTTGTATGATATTTAAAAAATGTATAATGAAGTTATTTATGTATGAATAAATAACCCTTAGTAAAAACCTTTAAAATACAGATATGGATAAAACTGAAGTTTAGTCTATGCAAGTGATGCTGAAGTGAATATTTGTGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6615
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 |
---|---|---|---|---|---|
ENSDART00000083890 | Nonsense | 676 | 2589 | 18 | 66 |
ENSDART00000144729 | None | None | 292 | None | 7 |
ENSDART00000146135 | None | None | 63 | None | 2 |
Genomic Location (Zv9):
Chromosome 20 (position 7691519)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 7525924 |
GRCz11 | 20 | 7513663 |
KASP Assay ID:
554-4379.1 (used for ordering genotyping assays)
KASP Sequence:
TCKGTGAGAATAACAAACWGGTTTTTTYCTTTAATTATTTTGCCAGTATT[T/A]GGAGGGTCACTTGAAGTTCCTTGCGTTCTTCCTSCAAGAGGCCAGTCTGT
Long Flanking Sequence:
TAGTTTAAAAAAGAGTTCCAAACACTTATTTGAGGTGTTTTTTTTGTTTAAGATTGAATATTGCTAAATGAAAATACAAAAAGACTAAAATCTTTTTTTTGAAGATATTTTTATGAACAATTTTTAAGTGTTGCACCTTAAAAAGGTATTATGAATCTTGCAAAAAGATGCATATCAGATAAAAATAATATTCATAATATAAATATTAATAGAAAAAGATATAGATCCTAAACATAAACACACTATATTTCCTCTATTAATAGCCTATTAAATGCTTTATTTTATTTTTCGAAATGTCTTCTAGTTTCTATTCAATCAAGATTATGTAAACAAAGTCTTGTAATTTCTCCTGGTTAACAGATGAATCATGTTGTTATTTGAGATAAAAATTGAGTATAGGATAAAAATATACTGAAAGCCTACTAAAGTGACTCATGTGATGCTAATCATTCTGTGAGAATAACAAACAGGTTTTTTCCTTTAATTATTTTGCCAGTATT[T/A]GGAGGGTCACTTGAAGTTCCTTGCGTTCTTCCTGCAAGAGGCCAGTCTGTACCTGGTCTGGAACAGAGCCAAAGAGATCTGGGAATGCCTGGTATCCGGCATGGATGTTTGTGAGCTGGATCGAGAGGTGTGTGGACGATGCAGTGTGATTTTTATTATTATTTTTTTATTTTTGTTTTTTTTATTATTTTGTGTGTGAGCATGTGTTCTTCTCTTTCTTTTCTTTTTGTTCACTGGTTTCCTTTGTTTTAGTTTATTTCATAAAATTCTTTTTTTTTTTTGTTAAGATGCTTAGGGAGGTGTTTTGTTTGATTAGGATTTATTACATATGGTTTTGTTTAGTTAGTATTTTCTATTTGTTTTTTTAAGATGCTAAGAGAGGTTTTTGTTTGTTTAAGATTTATTATGTATGGATTTGTATAGCTAGTATTTTCTATTTTTTTTTTTTAGATTCTTAGGGAGGTTTTTTGTTTGATTAAGATTTATTACATATGGTTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43384
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 |
---|---|---|---|---|---|
ENSDART00000083890 | Nonsense | 717 | 2589 | 18 | 66 |
ENSDART00000144729 | None | None | 292 | None | 7 |
ENSDART00000146135 | None | None | 63 | None | 2 |
Genomic Location (Zv9):
Chromosome 20 (position 7691397)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 7525802 |
GRCz11 | 20 | 7513541 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGAGATCTGGGAATGCCTGGTATCCGGCATGGATGTTTGTGAGCTGGAT[C/T]GAGAGGTGTGTGGACGATGCAGTGTGATTTTTATTATTATTTTTTTATTT
Long Flanking Sequence:
TTTAAGTGTTGCACCTTAAAAAGGTATTATGAATCTTGCAAAAAGATGCATATCAGATAAAAATAATATTCATAATATAAATATTAATAGAAAAAGATATAGATCCTAAACATAAACACACTATATTTCCTCTATTAATAGCCTATTAAATGCTTTATTTTATTTTTCGAAATGTCTTCTAGTTTCTATTCAATCAAGATTATGTAAACAAAGTCTTGTAATTTCTCCTGGTTAACAGATGAATCATGTTGTTATTTGAGATAAAAATTGAGTATAGGATAAAAATATACTGAAAGCCTACTAAAGTGACTCATGTGATGCTAATCATTCTGTGAGAATAACAAACAGGTTTTTTCCTTTAATTATTTTGCCAGTATTTGGAGGGTCACTTGAAGTTCCTTGCGTTCTTCCTGCAAGAGGCCAGTCTGTACCTGGTCTGGAACAGAGCCAAAGAGATCTGGGAATGCCTGGTATCCGGCATGGATGTTTGTGAGCTGGAT[C/T]GAGAGGTGTGTGGACGATGCAGTGTGATTTTTATTATTATTTTTTTATTTTTGTTTTTTTTATTATTTTGTGTGTGAGCATGTGTTCTTCTCTTTCTTTTCTTTTTGTTCACTGGTTTCCTTTGTTTTAGTTTATTTCATAAAATTCTTTTTTTTTTTTGTTAAGATGCTTAGGGAGGTGTTTTGTTTGATTAGGATTTATTACATATGGTTTTGTTTAGTTAGTATTTTCTATTTGTTTTTTTAAGATGCTAAGAGAGGTTTTTGTTTGTTTAAGATTTATTATGTATGGATTTGTATAGCTAGTATTTTCTATTTTTTTTTTTTAGATTCTTAGGGAGGTTTTTTGTTTGATTAAGATTTATTACATATGGTTTTATTTATTTATTTATTTATTTATTCAGTTTTTAAGATGCTCAGATAGTTTTTTGTTTAGGATTTATTGCATATGGTTTTGTTTGGTTTATTTTTTAAAGTTTTAATTTAGTTGTAGAATGTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15755
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 |
---|---|---|---|---|---|
ENSDART00000083890 | Nonsense | 1978 | 2589 | 49 | 66 |
ENSDART00000144729 | None | None | 292 | None | 7 |
ENSDART00000146135 | None | None | 63 | None | 2 |
Genomic Location (Zv9):
Chromosome 20 (position 7645997)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 7480503 |
GRCz11 | 20 | 7468210 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AACGACAATGTTGTGGAAGAGTTTGACATGAACGATGAGACTCTGGAGTA[C/A]GAGTGTTTTGGGGGGGAATACAGACCCAAAGTTTATGACCAGTGTAAGTC
Long Flanking Sequence:
ATACTTGGGTTTAATGCAAGCTAACAAACCCCTAAAGTGTGAAAAGTGGTAAAAGATTGCATCATGCATCATAATATTACAGTATTCTTGTGTTAAAGGATTCAATATGACTTGTATTTGAACGACACATTTATGAAGTTCTGCAGAGAGTCTATTTCCACAGTGCAGACTCTTTATGTACTTACTTCAACGGTTGTAATATCTAAAACATAAGCTTAATGTTTCAGGGAGTGTTTGCCCCTCCATGTGTATTTATGGGTCTCTGGAGGGCCATGCTTCTGTTTTGTATGTTTTATGAGTCTTAAAACTCTCCCAGATGCTTGGCTGTATGATGGTGTAGTTATTTTTTGAGGGAATGAAAGAATGTTTGGGTGACCATGATAAATATCTGTTAACATGCATTTTGTTTTCTTGTTTAGGGGTAGTGCACGAGGACGCTGGTATAAGTTTAACGACAATGTTGTGGAAGAGTTTGACATGAACGATGAGACTCTGGAGTA[C/A]GAGTGTTTTGGGGGGGAATACAGACCCAAAGTTTATGACCAGTGTAAGTCATTCATATTTCTTTGAATCAGTGTAAATAAATGATGTCAAAAGTACATGCACTCAAGTAGCAATATAATGAGAGATCATTAGGCAACAGCATTGTCCGATCACCAGGACAAAGTCATACAATACTCTATTTAAACATGCTGTATGTAAGTTTTTGACTCTTCTAAAGTATAAAAATACCCTAATACTTTTGCAGATATTTAAAGGGTCATGACACCCCCCCCCTCCTCTACTTTCAGTTCAGGTCTACCTCAGAATTTTTTCAAAAGATGCATCATACTGGGCATGGAGCTCCGCGAGCAAAGGGCAGGAGTGGGCATGGCCAGCAGGGGAGAAAGAACAACTGTTGTCAGTTAGCTCACAAAATGAGACACAAACCATGAGGAGACGCATGATTTTATAGTTTACAAAGTTAAATGCAAAAAAAGAAACAGTAATTTAATCTCCTGCTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43383
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 |
---|---|---|---|---|---|
ENSDART00000083890 | Nonsense | 2001 | 2589 | 50 | 66 |
ENSDART00000144729 | None | None | 292 | None | 7 |
ENSDART00000146135 | None | None | 63 | None | 2 |
Genomic Location (Zv9):
Chromosome 20 (position 7642101)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 7476607 |
GRCz11 | 20 | 7464324 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATCCTTTTTAATGTGTCATGCTATAGCAAACCCTTACCCGGATGTGCGA[C/T]GACGCTACTGGAATGCCTACATGCTGTTCTACCAGCGCATCAGTGACCAG
Long Flanking Sequence:
ATGCTCACTAAATACAAACCTAACAGATCACTCTGATCTTTAGGATCAAATAAACTAGAAATTCCAAGAGTTCAGTCAAAGCAGGGTGAATCTGCTTATATCAACTACGCCCCTCGCTGTTAGAATCAGCTTCCAGAAATGATCAGAGGTGCTCCAACATTAGGCACATTCAAATCGACACTAAAAACGCATCTGTTTAGCTGTGCCTTTACATAATGAGCACTGTGCTACGACCGACAGATCGCACTATTATGTCTTTCTTTTCTTTTTCATTCTTTTATAAACTGTTTTAACATTTTTATTCGTTTTTATCAGTTTATTTTTATAATTTTTATTGTTTGTTTTTATTTTATTGGATTGTACATAAAATAATTAAGTTGTCCCAAAAAAAATTGAGAATGGTGTTCTTTCAGCTCATTTTAATTAAGTAGTTTGAACAAGCAGTAAAGTAATCCTTTTTAATGTGTCATGCTATAGCAAACCCTTACCCGGATGTGCGA[C/T]GACGCTACTGGAATGCCTACATGCTGTTCTACCAGCGCATCAGTGACCAGAACTCACCCGTCCTGCCCAAAAAGAGCCGTGTCAGCATCATGAGGCAAGAAGCAGAGGATCTCTCTCTGTGAGTCTTAATAGCTTCTGCATGAGAGCTTGAATGTGGACTCGGTTATTAATGTTGATAATTCTTGTTGTCAGGTCAGCACCCTCCTCTCCGGAGATCTCACCCCAGTCTTCTCCACGACCACCCAGAGCCAACAACGACCGGCTCACCCTGCTTACACGCCTGGTCAAGAAAGGAGAAAAGAAAGGTCTGTTTGTGGAGAAGATGCCCGCCAGGATCTTTCAGGTACAGATTTGAATTATTATTATTTGTTTGTTCAGGTTTTTGAGATGCTTCAATAAAATAAACAAATTGAAAATTACTTTATATATACAGTGCTCGCGTAAATGAGTACATTCCCTTCTGAAAATCCTCTTGTTTTATTAAATAGTTATGTATAGTA
Associated Phenotype:
Not determined