ZMP
zgc:158452
Ensembl ID:
ZFIN IDs:
Description:
tumor suppressor p53-binding protein 1 [Source:RefSeq peptide;Acc:NP_001073639]
Human Orthologue:
TP53BP1
Human Description:
tumor protein p53 binding protein 1 [Source:HGNC Symbol;Acc:11999]
Mouse Orthologue:
Trp53bp1
Mouse Description:
transformation related protein 53 binding protein 1 Gene [Source:MGI Symbol;Acc:MGI:1351320]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa34186 | Splice Site, Nonsense | Mutation detected in F1 DNA | Not yet available |
sa14524 | Nonsense | Available for shipment | Available now |
sa34187 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa34188 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa21079 | Nonsense | Available for shipment | Available now |
sa34189 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa34186
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:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109973 | Splice Site, Nonsense | 192 | 1709 | 8 | 28 |
ENSDART00000128192 | Splice Site, Nonsense | 252 | 1888 | 10 | 43 |
Genomic Location (Zv9):
Chromosome 7 (position 54350746)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 52620596 |
GRCz11 | 7 | 52895666 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTGTTTTCCCTTTTTATTTTAAGAATTAAATTGTGTTGGTCTTTTAGGT[C/A]AGAAGTCACTTCAAGCTGTCCTTTAAAGCCTCAGGATGGGGAAAGCAGAA
Long Flanking Sequence:
TGTCTATTCAGTGTCCTTAAACAAGAACGGTGGTGGTGGGGTTCATAATATTCACAATGGTATTTTATTAGTTGTTGGTTTAACCATGGATGAGATAATGGCTTCTATGTTATTTTCTTTTCAATGACATTTCTTATCACATGTTCAAAAACAACAGCCAATATTGCATATCTATAATTTATATAATGGGTATAATTAAACAATACTTTCACTATAACGTAAATTAGAAGTGTAATAGAAAAAAATATATATTTCTGCGCCATTTTGAATTTTACTCGAATACAAATACAAATACAAATACTTTTCCCCCTCAACAAATACAAATACAAATACAAATACCGGCTGCTGCGCACATCCCTAGTGCACATAATGCTGGAGTGCTTTCAGTATGTATGGAAACAATCAATTTGAAGTAATTGGGCAGTTTTACCAAACGATAGCTTGACAATTATTGTTTTCCCTTTTTATTTTAAGAATTAAATTGTGTTGGTCTTTTAGGT[C/A]AGAAGTCACTTCAAGCTGTCCTTTAAAGCCTCAGGATGGGGAAAGCAGAAAGCTCAGTATTCAGGCTATACTTCACTCTCAGTTACCTGACAGTCAAGAAGATGAAGAGGATGTGCTTGTTTCTTCTCAGGATGACATGTTTGAAAAGGAGACCAATGGTGTGTAGTTATGTTTTCCACTTTCTATTTTTTTTACAAAAATGTATCATTGGGATAAAATTAAAGTGATTTAGCACAAATTGAACTGCAAAATTACATCTAATGTAAAATATTTGTATATCGGTAAAATTTTGTTATTTTTATTTATTTATTCTCTATCATTAAGATAGGAAGTTATTATTATGTAATATGTTTTATCTATATGGATCTTGCCATAAAATAGCCCTTAGTTGCTGATGTGGCAATAAATATACAAACTCAAAATCTATTTTTGTTTCTTGTTCTTTCCTAATTAAGTTTTTCTTTTTCTTTTTTTATTGGAACATGTTGACTAACAGGCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14524
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 |
---|---|---|---|---|---|
ENSDART00000109973 | Nonsense | 273 | 1709 | 9 | 28 |
ENSDART00000128192 | Nonsense | 333 | 1888 | 11 | 43 |
Genomic Location (Zv9):
Chromosome 7 (position 54351326)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 52621176 |
GRCz11 | 7 | 52896246 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGCCAACATCCACACCTGCACAAAGTCTGCGCCTGCTTCATCTGTCTGGA[C/T]AGGGTACCTATGTACAGGAAAGTCTTTCACAGTAAGTRTTTTAGCCTGAT
Long Flanking Sequence:
CAGTTACCTGACAGTCAAGAAGATGAAGAGGATGTGCTTGTTTCTTCTCAGGATGACATGTTTGAAAAGGAGACCAATGGTGTGTAGTTATGTTTTCCACTTTCTATTTTTTTTACAAAAATGTATCATTGGGATAAAATTAAAGTGATTTAGCACAAATTGAACTGCAAAATTACATCTAATGTAAAATATTTGTATATCGGTAAAATTTTGTTATTTTTATTTATTTATTCTCTATCATTAAGATAGGAAGTTATTATTATGTAATATGTTTTATCTATATGGATCTTGCCATAAAATAGCCCTTAGTTGCTGATGTGGCAATAAATATACAAACTCAAAATCTATTTTTGTTTCTTGTTCTTTCCTAATTAAGTTTTTCTTTTTCTTTTTTTATTGGAACATGTTGACTAACAGGCACCAAGGCTGACAGCAGTGTTTCAGAGCACTTGCCAACATCCACACCTGCACAAAGTCTGCGCCTGCTTCATCTGTCTGGA[C/T]AGGGTACCTATGTACAGGAAAGTCTTTCACAGTAAGTGTTTTAGCCTGATTTATTGTATTGTGAATTAGAGCTGAGCCGATAAACGATATTATATTTTTTTAAAATGTGTGTCGATAACAATGATAAACGCTGGACTTTTTTACTCTATATTTATCTAAAAGGAATCTAAAAGTATGTTGATATTAGGTATGCACTGAATTTTCGGCCACTGTAAATTTATCAGTTAAAAATATGTTATGCCAATAAATAGACCCTCTAATTTTTGTGGCTTTAGGTATTGTTGTGATACTCTTTTAAATCTGGAAACATTGTAAACTTGTATCAAGATATATATCGTTATCGTTCAATATAGAAGATAATCCGACCCGCTAGTTTTTCATGATACCTCAATCGCTGAATCCAACGCTAAATCGACAAAAAAAACACACATTTTTTCAATCCTGCAAAATTAATTAAACGCAAAATAATCGCAAAAAATGTAAATAATCTCATAAAAATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34187
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 |
---|---|---|---|---|---|
ENSDART00000109973 | Nonsense | 766 | 1709 | 12 | 28 |
ENSDART00000128192 | Nonsense | 826 | 1888 | 14 | 43 |
Genomic Location (Zv9):
Chromosome 7 (position 54356618)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 52626468 |
GRCz11 | 7 | 52901538 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGTGAGTTCAACTAAGGTTTCACCTCTCCGGCTTGAGAAAACCAAATCG[C/T]AGAACACACAGCCAAGTAGTTCAGGACAACAGAAAGTGAACTCAGACAAC
Long Flanking Sequence:
CTCAGTCAGTCTTAACAGCGTCATCCCAGAAAAACACTGGCAACAAAGAAAAACATGATGGTCAAAACCAGAGACTCAGTCAGCCTATGCTACACAGCCACAGTGTTACTACAGACAGTGTTAGAAACGTAGAGGAGGAGGAGCAGATGGAGGAAGGTGAGATTAAGAGTACAGTGAAGGGGGATGACACTGGAATAAACCTGGCTTTGTCTCAGAGTCAGGCTCTTTCTCCAGAACCCATGGAGGAGGAAGAGGAGAAAGGAGAAGCCAGCATCAGATCGTCTAGCAGAGAGGAGAGCTTCAGTGTGATGGTGCTGGAAGAGAGCCAGAGGGTTTCTCAGGAGAAAGTGCAGAAGGGGAAATCACCACCGTTCAAAAGCTCCTTGCAGCCTGTGAGTGGCTCCATACAGGACAAACCTGAAGCCCTGGCAAAGATCTCTGGGTCTCAGCCAGTGAGTTCAACTAAGGTTTCACCTCTCCGGCTTGAGAAAACCAAATCG[C/T]AGAACACACAGCCAAGTAGTTCAGGACAACAGAAAGTGAACTCAGACAACGCAGCCAACAAAAGTCTGAGTGACAGCTCTGGAGGTGGGATTAAGACACAAACAAACGATCTATTATCTGTGCTGATTAACTTACTTGTGTTCAGGAAATCCAGCTAGCTGATTTCTTTTTCTTTCCTGCTCAGAGCTTCCGTTTCACTTTACACTGCCCAAAGAGGGTGAGCTGATCCGGCCTGCAGTGAGTGCTACTCCTCCACAAATTAGTCTGCTGAAAAAGACACCAAGACACAGCACTCCTATTGGTGAGTCTTTCTTTTTATTCTCTAACATTTGGGTTTAAATGTACGTAATACCAGACTGAAACTGCACACCCTGCCTTCTAAGCTCCTATTTGTGGTGAAGCATCTTTCTTTTTTTTGAACACGTACTGATGTTTTGCAGAGATGAACTCATTCTCAGAGCCGTCAGTGGGCGACGTTACCAGGGAGACAATGGCAAACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34188
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 |
---|---|---|---|---|---|
ENSDART00000109973 | None | None | 1709 | None | 28 |
ENSDART00000128192 | Nonsense | 1012 | 1888 | 20 | 43 |
Genomic Location (Zv9):
Chromosome 7 (position 54365958)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 52636039 |
GRCz11 | 7 | 52907362 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACGGTCGTGGTGTCTGTGTAGTGAGTTTATCAGACCAGTTCACCCGGCCT[T/G]AAGTTCAGTCTGTTTTCACTCCAAGATGTAAACAATAGTCTGATAATGCG
Long Flanking Sequence:
AATGTAAAAAAGGGAGAGTCTGGAGGGAGTCTCAGGGAATGAAATGAAAACAACATTTATTTTCTGTTGTCAATGTCAGAGGTGGGTAGTAATGAGTTACATTTACTTGAGTAAAATTATTGGGTAACGCGTACTTTTTGAGTACATTTAAATATGTGTACTTTTACTCAAGTAAATTATTAGAGAAAAATCATAACTCTTACTTCGCTACATTTCGCGGCGTTCTTCTGTTACTGTCAAATGATAATAAAATGATCCATATGTTTTGTTTGCAAATATCGCAAGGCCCCGCATTGGAGAGGTTGTGTCACGAGAGGTTGCTATAGAGACGCGTCTTCCGCTATCGGTATGGGTCTGCGCAGCCGCGCGCCTGTGTCAAATGATGGCTGACAAGGGAGACGTTCGAGGTATACTGCGGTCACGCCATGGCCATCTACGGTTCCGAGAAGGACGGTCGTGGTGTCTGTGTAGTGAGTTTATCAGACCAGTTCACCCGGCCT[T/G]AAGTTCAGTCTGTTTTCACTCCAAGATGTAAACAATAGTCTGATAATGCGATGCATGCTGTACATTGAACTGACATCACAGCATATACATGAATTCCAGCTCCAAACTGAAAAAAACTAGTGGTAAGTGTCCAAATGATCCCATTTTGAACCTTATTCATGTTAACTTTGCAGGCCCATAGCTAGGGGGGTTCGGGTGGTTGGAAAAACCCATCTCTCAATGACAAAGGTCCAGAATTTCTCCCATACATGAGCTCATTTGTCTTATTTTGACTGCTATGTCATCATAAACAGTGAAATTAATCCATTGAAAAAGGCTTTAGGACCAAGAAGAATCCTATGTTAAAATTAATTTGAAAACTAATTTGGCTATTTTTGTTATCCATGAATTTTCAATCAAATCAAATTGACTTTTTTCACAAAAAAATGTGAAGTTCTTTCTTTTTCTTTCTTTCTTTCTGTCTTTCTTTCTTTCTGTCTTTCTATCTTTCTTTCTTTCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21079
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 |
---|---|---|---|---|---|
ENSDART00000109973 | Nonsense | 1008 | 1709 | 17 | 28 |
ENSDART00000128192 | Nonsense | 1163 | 1888 | 28 | 43 |
Genomic Location (Zv9):
Chromosome 7 (position 54372854)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 52642845 |
GRCz11 | 7 | 52913970 |
KASP Assay ID:
2259-9515.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTTAGAAGCAGATTCTGAAGCTCTGGTCAGCGGTCTGTTATCCCCAGCC[C/T]GAGAACGGGAAGCTCTCGACACTTTTGACAGACCTCAAACACCCGTCCGA
Long Flanking Sequence:
ATGATTGTGCTGCACTATATCAGGCTAATGCAGAAATACAACTAGAACTATACCCAACTGTTCATATAACCTTTCGACATAATAGTTGAAAAGCAGCTTTAGATGTTTGAACCATGACATGACTTACACATCCTTCATAATTGCAGGATTTATTTATATAAAGCATCTTGTAGTCATTAAATAGGAGATGCTACAATTTAGTTAAAGAAATGTTCTGTGAAGTGAAGTGTAGCACGTTGTTGTTTTACACATGAACAGTTTATTATTTAGTTTAAATTTTCATCTATTACATCTTTATTTGCTTTCATTTCTACTTCTCCAACAGGCAGCCAAGCCAACTGCTCAGTCCCACCATTACTAATGACTCGGAACTGTCTCCAAATTGCCCAAAAGAGACTTCAAACAGCAGCAGAGCTTCAGTCACAGAAGCTGTATCTCTAAATCCTGGGGCTTTAGAAGCAGATTCTGAAGCTCTGGTCAGCGGTCTGTTATCCCCAGCC[C/T]GAGAACGGGAAGCTCTCGACACTTTTGACAGACCTCAAACACCCGTCCGAAAGAAAGCTGTGTCACAGCAAACCAGTGTAGATATCAGCTCAACCACCAGTCCACCCAGCAAAGTAAGAAAGCTGTTGTGTATTTTAGTATAAATACGTAAATCATGCATTAAAATGTAATTTGTTATATGTTTTCTCCTTTGATTTCAGAAAGCTGTTTCTCAGCAAACAAGTTTTGATCTGTCTGGACCACATAACCTGTCTGGAAGGGTAAAAGACTTCACTTAATTTTTATAATGAGCTTGCAAGAAATACAGTGTTATTAAATATATAAAGGACTGTAGCTTTTCAGAAGTGTCTTTATGTTTTATGGTTCTACTAAAAGGGAGAACCGAGCACCCCCACCAGAACCCAGCCAGTTCCATCATTGCGCAGGCATGTTCGCACCATCCAGGAAGTCCGAACAACAGTCACTCGCATCATTACAGATGTCTACTACGAAGATGGCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34189
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 |
---|---|---|---|---|---|
ENSDART00000109973 | Nonsense | 1292 | 1709 | 21 | 28 |
ENSDART00000128192 | Nonsense | 1460 | 1888 | 34 | 43 |
Genomic Location (Zv9):
Chromosome 7 (position 54380545)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 52650536 |
GRCz11 | 7 | 52921661 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGAGAACCGTTTCCGCCTTCTGTTTGATGACAACCAGGAGTGTGAAGTG[C/T]AGGGAAAGGACATCTTGCTCTGTGACCCAATTCCTCTGGAGACGGAGGTC
Long Flanking Sequence:
CTCACTTTAGGAAGCAGCATGCCAGTATCATAAATTACAAAAAGAAAATGCAGGAATAGAGAATATAGGAAAAATAGGATTTCATGGCTCATAAGTATCAATATTGAATCAACTACTTCTTAAAAAAACTTAAACTTAACTTAGCTTAGTCTTTTCTTTGTATTGCTTATTCCCTGTTAACACTGACTATCAGAGGTGGCAGGCCAGGCCAGAGAGGTGGTGCTCATGCCCCGGGTGGTGCGTCGTCCTCAGAAGAGGAGCCATTTGCACAAAGGCATGTCCAGATGCCCATCAGCCCAGTTGAGCCCAGTGCTACAAGCCACTCAGAGTCCCTTAACACCACTTCCCCGGACAACAGCACTGGCTCCAGCAGTTTTGTTGGGTTGCGTGTGCTGGCCAAGTGGTCATCCAACTCCTATTTCTATTCTGGGAGCATCACTCGAGACCTGGGAGAGAACCGTTTCCGCCTTCTGTTTGATGACAACCAGGAGTGTGAAGTG[C/T]AGGGAAAGGACATCTTGCTCTGTGACCCAATTCCTCTGGAGACGGAGGTCACTGCCTTGACCGAGGAGGAGTACTTCAATATAGGTGAGCACTGCAGTCCAAACCTGTTGTGAGCCATTCATTTAAAACCATGGTATAACGATTTATAACACCACCAGGATTGTTTTTATTTTAATATTATTCCAAGAGCCTAACACTATAACAATGAGCATGATTTTGCAGGTTGGGCTGTAAATGATCTGTCCATCCATCATTCTATCATTCTGTTTTTCATGGATTCATATTGAACCATTTAGAACGAGGCTTTTACTTTGATATGCAATACTGTCCGTCTGTCAGTCGGTCGGTTGGTCTATCAATCTGTCTTTTTTATCTGTCTGTCTATCTATTTATCAGTCGTTCTACCTGTCTATCATTTGTTATGCATTGCTGTCTGTTGGTTGGTCAGTCTATCTGTTTGTCTTTTTATCTGTCTTTATCTGTTATTCTATATATTGCTC
Associated Phenotype:
Not determined