ZMP
tprb
Ensembl ID:
ZFIN ID:
Description:
nucleoprotein TPR [Source:RefSeq peptide;Acc:NP_001025294]
Human Orthologue:
TPR
Human Description:
translocated promoter region (to activated MET oncogene) [Source:HGNC Symbol;Acc:12017]
Mouse Orthologue:
Tpr
Mouse Description:
translocated promoter region Gene [Source:MGI Symbol;Acc:MGI:1922066]
Alleles
There are 15 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa37088 | Essential Splice Site | Available for shipment | Available now |
| sa23754 | Nonsense | Available for shipment | Available now |
| sa14064 | Essential Splice Site | Available for shipment | Available now |
| sa18388 | Nonsense | Available for shipment | Available now |
| sa23753 | Nonsense | Available for shipment | Available now |
| sa32305 | Nonsense | Available for shipment | Available now |
| sa23752 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa37088
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000017941 | Essential Splice Site | 465 | 2352 | 12 | 50 |
| ENSDART00000109614 | Essential Splice Site | 466 | 2316 | 13 | 52 |
Genomic Location (Zv9):
Chromosome 20 (position 34088499)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 34161012 |
| GRCz11 | 20 | 34063891 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAGAAATCAGTTTCCAGTCTCTCTGCTAAATTAGAGCAAGCTGTCACGG[T/C]GAGAATTGAAAAGTTTTATTACATGTCACATTACCAGATGATTACTTTTT
Long Flanking Sequence:
TTTGCTTTTTACTGTTTTTTTATGTTTATTTCTGCAACTTTGACTAGTGGTTTTTGATATAAAATGTATACAAGTTTTTCATTTGCCACTCCAGGAGCTGCTTCAATTCTTACAGAAGAGCAGGTGACCATAATGTCCCCCACTGCTGCTGCAGTTGCCAAAATGATCAAACCAGGCATGAAACTCACAGAGGTGATAACCTTACTTCTGATCAGTTATACCAGTCTAAGGTTCATTTTCATAAATCATTTTTATGAGGTAAAGTAAGCTAATGCACATTTTCCAATTTTTTTTTTTGTAGATCTATACCGCATACGTTGAGACCCAAGAGCATTTACAGCGTGAAAAACTCGAGAACAAGCGACTGCACAAGTACCTGGATGACATTGTGCAGGAAATGGAAGCAAAGGCTCCTATACTGAAAAGACAGAGAGAAGAGTACGAGCGCATGCAGAAATCAGTTTCCAGTCTCTCTGCTAAATTAGAGCAAGCTGTCACGG[T/C]GAGAATTGAAAAGTTTTATTACATGTCACATTACCAGATGATTACTTTTTATATTTATAAAACCAAATCTACAATTGTGTATTTTTTGGTACTTTTCAGGAGGTACATCGCTTGCAAAAAGAATCGGATGAAAGCAACAAGCGTGCATCAGTTTTGGAAAGAGATAACCAGAGGTTTGAGGTTCAGCTGGCTGACATGGCTCAACAGGTGAGGCCTGGAGGCACAACTTTGCGATCAGTGTTTCATGCCAGAGCAAAAAAAAAAAAAAAAAGATCTAAGTTACAATAATTTTAACATTGTAATCTCAGGTGCGAGTTCTTCTCGTTGAGCTGGAGGAAGCACGTGGTAACCATGTTATGCGGGAGGATGATGATGTGGGTTCGGCAGATGTGAGCAGCACATCGGAGGTTATTTCTCAGCACCTGGTCACTTTCCGTAGCGTTGAAGAGCTGCAGCAGCAGAACCAGCGACTCCTAGTGGCGCTCAGAGACCTTAGTGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23754
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 |
|---|---|---|---|---|---|
| ENSDART00000017941 | Nonsense | 1033 | 2352 | 23 | 50 |
| ENSDART00000109614 | Nonsense | 1034 | 2316 | 24 | 52 |
Genomic Location (Zv9):
Chromosome 20 (position 34085235)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 34157748 |
| GRCz11 | 20 | 34060627 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAAACAGAACTTGCTGGAAGAGAAAAACAAAGCTGTTGCTGCTGTAGAG[C/T]AAGAGGTAGTGAATTTACACCTTGGATCACTACATTTTACCTGTTTAAAA
Long Flanking Sequence:
GCAGGGCAGTGAGAGGGACATGGAGGTTCTGCGTGCCCAGATAAGGCAGACTGAGAACAGAATTGAAGAACTGACAGAGCGACTTAAAAACACTACTGCCAGTATGGAGCAATACAAGGCTATGAGTCTTAGCCTGGAGGAGTCTCTAGATAAGGAGAAGCAGGTAGTTAGACATTTTCATTTATTCATTTTTTTTTTCTTCGGCTTAGTCCTTTTATTCGGTGTATATGAATATCACATCAAATCACAGTGCTTGGCTATTAAAGGCTGGCTTAGAGTACATTTTTATACTACAATTCATTGGCACTTTTGTTTGATTTTTAGAATTTTGTTTGTTTGTTTCCCATTTCTAGGTAACTGAGCAAGTTCGTTCATCTGTAGAAAACCAAGTGGAGGCAGCTCAGGAGCAGTATAAACGGCTAGAGCAGAAACTGCTGGAAATGGACAAGGAGAAACAGAACTTGCTGGAAGAGAAAAACAAAGCTGTTGCTGCTGTAGAG[C/T]AAGAGGTAGTGAATTTACACCTTGGATCACTACATTTTACCTGTTTAAAAAAAGGCCTGTTTTTTTATTAATGGCTGTCCTGTGCAAAACGATAATCATTTTAAGGACCTCTTAAAGTGACTGTTCACTGAAAATTCTGCCATAATAGTCACATTTGACTTGTTCTAATACACTTAGAATTTTTATGTTCTGCCAAATTATGTATATTTTAAAAACTGTTGGAAGCCTGTAACCACTGAATACCATAGTAAAGAAAACAAATACTATAGAAGTCAACTGTTACAGGTTTCCAACATTTTTCAAAATATATTTTTTTTAGTTTTTAGCAACTGCTTTGTAGCAAGACATGGATAAGTGAAGGATGGCAGAATTTCATCTTTAAGTGAACTTTAAGATTACATTAGCCATGTTTCCATTCAAAGATGAGATTTAAATTCATGCACAAAACTGGATTATCACATTAAAGACTTTCAAATAAAGCAGCTTTTCAATCCAATGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14064
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 |
|---|---|---|---|---|---|
| ENSDART00000017941 | Essential Splice Site | 1573 | 2352 | 32 | 50 |
| ENSDART00000109614 | Essential Splice Site | 1565 | 2316 | 33 | 52 |
Genomic Location (Zv9):
Chromosome 20 (position 34079105)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 34151618 |
| GRCz11 | 20 | 34054497 |
KASP Assay ID:
2261-4611.1 (used for ordering genotyping assays)
KASP Sequence:
ACCAAGAAGGCCATATTAWTGGCCAAGCAGAAGATCAGTCARCTTACTGG[T/A]GAGAACTGACTCTTTTTGAGAWTAGTATGTGCTTTKAGTCTTTTTCTTTT
Long Flanking Sequence:
AACATTTGACCTGAAGAGATCTTATTTGTGGGTTTTTTTAATACCATTAATTGTTTAAAAACAATTGTGCCAGTGTTCGATCCAAATCAGTTCTTAAAAAAAAATAATATTATTGATGATAGACCTGCTTTCTGCTTACTGACTGGTTTGCTGTTTATCAATCAAGTAAAATATAGCTTGGCATCCCTGTTTTTCTTGTGTGTCTTTGCACATCCTCCCTTACAAACTGAACCTTTTGAGATGAGACTAAAGTTATCGGGTGTCTTTCTCATAATGTGTCATTTCTGTTGTCCTCTGCAGACTGTAGGAGAGCGAGAAATGGAGGCCCGCAGTGCGCAGGAACAAGCCTCTCGTTTGCAGACAGAGTTAACGCGTCTCAGACAAGAGCTTCAGGAGAAATCATCTCAGGAGGAGCGTCTCAAACAGCAGCTGACTGAAAAGGAGGAGAGGACCAAGAAGGCCATATTATTGGCCAAGCAGAAGATCAGTCAACTTACTGG[T/A]GAGAACTGACTCTTTTTGAGAATAGTATGTGCTTTTAGTCTTTTTCTTTTCTTTATTATTTTTCTACATCCAGGTATAAAAGGACAGTTTCAGAAGGAGAACGAGGAGCTGAAGCAACAAAAAGAGGAGTTGGAAGTGCGTGTGAGTGCGCTGAAGTCTCAGTATGAGGGGCGTCTGAGCAGACAGGAAAGGGAGCTACGAGACCTTCGCGAACAGCAGGAGAGACATGGAGAACAGAGGGATGAACCACAAGAGCAGGGCTCCAGCAAGGTAATGCCACACAATCCTATAAATGCAAGCCTATTCGTAGTTTTCAGTCAGGTGATCTGGAGTGTAAAACGTCTATACAACTGTGATAAACACCTTACCATTAGTTTCAAGCCACAAATATTTGGATCAGCCCTCATAAGAAAAAAAAAATGGGGCCAGTAAAATCTTTTAGATGCTTCTGATCCTTATACACTACTTTCCGTCACTAAATATTAAGCTTAATCTGGTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18388
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 |
|---|---|---|---|---|---|
| ENSDART00000017941 | Nonsense | 1615 | 2352 | 33 | 50 |
| ENSDART00000109614 | Nonsense | 1607 | 2316 | 34 | 52 |
Genomic Location (Zv9):
Chromosome 20 (position 34078906)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 34151419 |
| GRCz11 | 20 | 34054298 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGCTGAAGTCTCAGTATGARGGGCGTCTGAGCAGACAGGAAAGRGAGCTA[C/T]GAGACCTTCGCGAACARCAGGAGAGACATGGAGAACAGAGGGATGAACCA
Long Flanking Sequence:
GTGTCTTTGCACATCCTCCCTTACAAACTGAACCTTTTGAGATGAGACTAAAGTTATCGGGTGTCTTTCTCATAATGTGTCATTTCTGTTGTCCTCTGCAGACTGTAGGAGAGCGAGAAATGGAGGCCCGCAGTGCGCAGGAACAAGCCTCTCGTTTGCAGACAGAGTTAACGCGTCTCAGACAAGAGCTTCAGGAGAAATCATCTCAGGAGGAGCGTCTCAAACAGCAGCTGACTGAAAAGGAGGAGAGGACCAAGAAGGCCATATTATTGGCCAAGCAGAAGATCAGTCAACTTACTGGTGAGAACTGACTCTTTTTGAGAATAGTATGTGCTTTTAGTCTTTTTCTTTTCTTTATTATTTTTCTACATCCAGGTATAAAAGGACAGTTTCAGAAGGAGAACGAGGAGCTGAAGCAACAAAAAGAGGAGTTGGAAGTGCGTGTGAGTGCGCTGAAGTCTCAGTATGAGGGGCGTCTGAGCAGACAGGAAAGGGAGCTA[C/T]GAGACCTTCGCGAACAGCAGGAGAGACATGGAGAACAGAGGGATGAACCACAAGAGCAGGGCTCCAGCAAGGTAATGCCACACAATCCTATAAATGCAAGCCTATTCGTAGTTTTCAGTCAGGTGATCTGGAGTGTAAAACGTCTATACAACTGTGATAAACACCTTACCATTAGTTTCAAGCCACAAATATTTGGATCAGCCCTCATAAGAAAAAAAAAATGGGGCCAGTAAAATCTTTTAGATGCTTCTGATCCTTATACACTACTTTCCGTCACTAAATATTAAGCTTAATCTGGTAAGAAATTAATATTAATGCACATAAATGTGGATGTATATGTATATATAATATAATTTTATAGGGTATTTCTCTTTGACTTCAAGCTATTAACCATCTTTAGATACCTAATGTTCTTTTACTTTCAAATGCTTCAAAATGCTGTTTTTTTCCATGTTTAAAGACCCAGGAACCACAAAGGACAACAGAACAGCGACAGATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23753
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 |
|---|---|---|---|---|---|
| ENSDART00000017941 | Nonsense | 1929 | 2352 | 39 | 50 |
| ENSDART00000109614 | Nonsense | 1921 | 2316 | 40 | 52 |
Genomic Location (Zv9):
Chromosome 20 (position 34073698)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 34146211 |
| GRCz11 | 20 | 34049090 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGAAGAAATGGATGAGGAACCAGGACCATCTCAGTCTGTCCCTGGAGAT[C/T]GAATGCTGCCCCATCCATCTGAGACCCATCGAAGCCCAGAGGAGCCCGAT
Long Flanking Sequence:
GTTAAAGATGTTGTGTGTTTCATTTCAAGTCCATCATGTTGGTGTATAGAGCCAAAACTTTTTTGTGAATTGTGCAGATGTCCCAATATTTATGGACCTAGCTGTATATATGAGTGAATCATCTCTATATGAGCAAGTTTTAGAAGCATTTATTATCATTAAGATTAATTTACTACTTAAGTGAAGTCTTTAATCAAGAGGTAGTTCAAAAAAGCTGAATCATCCAGTAATGAAATGAGTATTGACAAGTGAGTCGTTGAATCAATTAATAAAAAGCTTTTTAGTTATTTATTCTGAATTGTGGGAAACTCACAGTCTCAAATGGAAGCAAAAAAAAAAAGTGCTTTAATCCAAGATCAGTTCCGGTGAACAGGTCAGAAGTGTGTAACTGACTTAAATGTTTTTTTTCTTCTCATGTCTGTTTGAAGGAGCTGGAGAACTACTCTACTCTGGAAGAAATGGATGAGGAACCAGGACCATCTCAGTCTGTCCCTGGAGAT[C/T]GAATGCTGCCCCATCCATCTGAGACCCATCGAAGCCCAGAGGAGCCCGATCACCACGTCATAGTCATTGTTAGTGACACCGAGAGCGAAGGAGAACAGGAAGAGGAGTCTGAGGAGGAGGAGGAGGAAGAGGAAGAAGAGCAGGTGTGTCCTCGCACTGCAGGTCAAATTCAGTGATATTCAATCCTGTTATATAAACCACTTATCCCTGCTTTAGGATTATGAGGAGGAGGATGAGGAAGAGGAGGAAGAAGATGATGATGATGATGAAGAGGATGGAGGGATTGGGGAAGAGGGAGATGAAAGCAATGAGGAGAGTAGAGACGACAATGAGGCCTACGAAGGAGATGACACAGAGGTAAAGATCTGCACTAGTCAGAATTTAGAAGTGGAGGTTTAAAATTATAAAACTGAGGTCTCGTTTACACTAATACATTTTAGTTTAAAAATAAATAAGTTTTGCTACGGTTACGCCTTTCGTCCAAACTACCCTGGAGTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32305
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 |
|---|---|---|---|---|---|
| ENSDART00000017941 | Nonsense | 2201 | 2352 | 46 | 50 |
| ENSDART00000109614 | Nonsense | 2165 | 2316 | 48 | 52 |
Genomic Location (Zv9):
Chromosome 20 (position 34066676)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 34139189 |
| GRCz11 | 20 | 34042068 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGTCTTTTGTGCTGTGCAGGTTTAGGCATGTATGAGAGCTCTGTTTTTT[T/A]GGGATCTCATGAGGATGAGTCAGGGGGACGCAGTGTACCCACAACCCCTC
Long Flanking Sequence:
ACCCAATGGTGAAAAACTTGAAAGGCTGATGACTTTTAATTTGCATGTTGTTTATGTATTATTTTTATCTTCTGCAGGTTATGGGTAAAACATGGTAATTCTAATAGTTTGAGAACATGTATGGTAATATTGGAAATCACCAATCTACAAACTGTATATCAGTGTCAATTGTCATGACCAGCTACTACTCATCATGTCATGTTTGCTGTTGTGTTTTGTTATTATTACTTAATCATATTACCACAAAACTGATTTGTTGTTGTCGAATGAAGTTCTCCACAGGTGGCAGGTGTACCACGCTTTCGATTCGGGCTTTTAGATGAGCTCCCGCAGACCAGCTCCTCTCACTCAGACCTCAGTCAGCTGCCCTCACAAGGTCAAACACAATCATTTTAAATTTAGAGATTATCAATTATAATGTCAAACATTAGTTTGTTCAGTTTTTTAAAGGTGTCTTTTGTGCTGTGCAGGTTTAGGCATGTATGAGAGCTCTGTTTTTT[T/A]GGGATCTCATGAGGATGAGTCAGGGGGACGCAGTGTACCCACAACCCCTCTGCAGATCAGCGCTCCTGGTAAATAACGCATGTTTTCTTATTTAGTTTTTTTTAGTCAGACTTTCTTGTTGTTCATCATTTAGGCAGAGTTGTAAAATTCTGTTATGATCTATTATAACCTGTTTATTTATTTAATTATTTTATGATAATTAGATATTTTAATAGCTTCTCTTTTCATTTACATTTATATATAATATTGAACATGCAGGATGAGCATAGACTATATTTTACATCCATCTATTTAGAACTGATAAATAAAGTCTGTGCATCATTGTGTGTGTGCGTGCGCATATCAGTACACAAGTAGTGGTAATAATTTCAAACATTTCAAATTTGTTCAGACCAGAGGTTTTTATTATAGGGGGGTAATTCCCGTTTATAAATGAGTATATAAAACTTTCTGGTGCATAGTGGTGTAACGGATCACAAATCTCACTGTTCGGATCACAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23752
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 |
|---|---|---|---|---|---|
| ENSDART00000017941 | Essential Splice Site | 2339 | 2352 | None | 50 |
| ENSDART00000109614 | Essential Splice Site | 2303 | 2316 | None | 52 |
Genomic Location (Zv9):
Chromosome 20 (position 34064252)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 34136765 |
| GRCz11 | 20 | 34039644 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCAGACAGTGGACTGGTAGTCGAGGTTCTAGAAGCATTGTGAAGAGGGG[T/A]GAGACTTTTGTTTCTTATTTGTTAGTTTCTTAAACTTTTATTTCCTTCCT
Long Flanking Sequence:
ACATGCTTCTCAGTCTGTGCCGATGGTGAGCACCTCTACCCCAGGCCTCAGTGCTCCAGCAGTGGAGGAGAGAGACGACATGTTCCTGGATGCAGGAGACAGGTGAGATTTTTGAGTTTTGAGACTTTTCAACATTTTCTCTTATGATTTTGCCATGACAAGAATCCATATATATTAGTATTTAATGGGAACTTTGATAAATGTTTGTGCAGTGCTGAAGCTTCACTTGAGGCCGTGTCTCAGACTGAGGCAGAAGAAGCAGCGCAGCCTTCAGATGATGCAAATCTGCCTTCAACAAGCCAGGAACCATCATCTAGTTCAGCAGGTACAAACACAATAATATTAGACAAACCACATGCAATCTCTTATTTCTGTTTCACTAACTATGTGTCTCGCTTTTCTCTTTCAGACACAAGCAGCTCTCAGCCTCCTAAAGCCAGGAGCGGCTCTGGCAGACAGTGGACTGGTAGTCGAGGTTCTAGAAGCATTGTGAAGAGGGG[T/A]GAGACTTTTGTTTCTTATTTGTTAGTTTCTTAAACTTTTATTTCCTTCCTTCCTTCATACATTTTCGCTTTTAAGCGGGCTGCATTTACAAAGTATAATTTTAACATCTTTCTTGCTATAGATGGACTGAGTGTTATGGGTGTGAGAGGACGCTTTGCCAGATGAAGCAAAATCCCAGCAGTCTTCATTCTAGTCTTCATCCTGAACTATTGGCTCCACAAGAACAGCTGTGCTTTATTCTGCTTCAGGACTTCAAGTCAGTGTATTATAGCTGTCGTTTGTTAGTTGTATGCTCTGAGCAATCCATTGTTGTTATTTTTAATGATTCTACATCCATAAAATAAATTGTTTTGAAGAAAGAGATTTTTGTTTTGTCTGTGAAGATGTGACCGGTTGTTTTCCACTGCATATTAGACGAGTGCATGAACATGTACTGTGAATGGCAGGAGGTAAGGAGATGGATGACTCAGATTTTCTGAGTGTCTTTGCATTTGAAGAAG
Associated Phenotype:
Not determined