ZMP
si:ch211-49j11.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:A2BFG9]
Human Orthologue:
UBASH3B
Human Description:
ubiquitin associated and SH3 domain containing B [Source:HGNC Symbol;Acc:29884]
Mouse Orthologue:
Ubash3b
Mouse Description:
ubiquitin associated and SH3 domain containing, B Gene [Source:MGI Symbol;Acc:MGI:1920078]
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa6983 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa33625 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa11071 | Nonsense | Available for shipment | Available now |
| sa40459 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa6982 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa6983
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 |
|---|---|---|---|---|---|
| ENSDART00000087128 | None | None | 599 | None | 13 |
| ENSDART00000143434 | Essential Splice Site | 43 | 643 | 1 | 14 |
Genomic Location (Zv9):
Chromosome 5 (position 31490052)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 29251409 |
| GRCz11 | 5 | 29851562 |
KASP Assay ID:
554-5412.1 (used for ordering genotyping assays)
KASP Sequence:
GAAACAGCCTGGATGTTTTGCTGTCAATGGGCTTCCCAAAAACCAGGGCG[T/C]AAGTACCAGMGTTTCATCTCGAGCATCACGCAGCTGTAATCACAGCTGTA
Long Flanking Sequence:
CAACATTTTCGAGCGCACAGCGAGACGCGAGAGACTCCGGCGGATGGTTTTTCTTCCCTTGACAGGCACCGACGGAGATGGCTGTCGATACGCGGACTGAACGAGATTGACTTCCGACTGGTGACCCCTTTCTCAAACTGTAATGACATGAGCGCTCCAGCAGGAAGCTCAAATCATTTTGTGTTTGGAAACATTGTAGCGCGTCCGCCGAGACTTCTGTCTGTCCGACTAGGGGAATAATGCGGAGCGTTCATGAAGCAGCCTTCACGGTAGATACTGTAGCGATGTTTTAAATGTGTGTCGTGTCCGTTCGTTAGGACGCATCAGAAGTGAGCAAACCGCTGTTCTCGAGCCCAATGGAAAGCTGAACCATGGCAGCGAAAGAAGACCTCTATGCCAAAGTCGCTCCACGGATGCAGAGGCAGAACCGGCCAGCAACTGTCAAACATGGAAACAGCCTGGATGTTTTGCTGTCAATGGGCTTCCCAAAAACCAGGGCG[T/C]AAGTACCAGAGTTTCATCTCGAGCATCACGCAGCTGTAATCACAGCTGTAGCCTGAACGTTGAGAGGACAGACGCATGTGATAAGAGCTCTAGTACACAAACACGGCATATATTTATTAAAACACTGTAGTGAAGTTGCCTTTGTAATGGCGTCGGTCTGTTGTGTCATTGATTAACATGACGAAGTGGGAAATGGGCTCAATCGCCGAAGGCATAGTGAGTGTAAAGTTGTTTTCCTGTTGCCTCGTTAAACCGTGTTTTAGATGAAACCCTGCTGCATGCGTTCAGGGCAGGACTTGCTCCTGCTACCAGCGGATGAGGTTGGACCGCTGGGAGGTCAGAGCATCGCTGTCCATCGTATTGGCGTTGTGTCCGCGCATCCATAATGACTGTCAGCTGCCCAACATGTTTTTCAGTAGTTATCCCAGCGTATTGGCTTTTGACTAGCCTACACACTGGAATGGGGAAACGTCATAATTTAAAGATTTAAAACTATTTAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33625
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000087128 | None | None | 599 | None | 13 |
| ENSDART00000143434 | Essential Splice Site | 43 | 643 | 2 | 14 |
Genomic Location (Zv9):
Chromosome 5 (position 31519973)
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTGTTAC[A/T]GGCTAAAAGCTCTGGTTTCGACTGGGGGCAGAAATGTACAAGCAGCCTGT
Long Flanking Sequence:
CAGTGTATGCTTCAACTCTTATAGGTTGCTTTGGCTCATATGACCCTCTTTAAAATAATCTGCAAAAGTAAGCCTCTTTAATATTCATAAATGCCCATAAATAAGTGATTATCCAGCTTTCCCAGTGATGTTCAGGAGACGGTCTAGACTCTTATTACAGAGCTTGCTTAGCCTGCATAAGTGTGATTTCATGCACGATAAACCATATATTCTTAAACCGAGATGTGGACTACTGAGGAACATCTCTGAGAAATCAGATCTCTGAGAAAACTCCTTAGCACTAATGTACTGATAAACATCCTCCGGAAAGAAGGCCATTGATTTTGTGACCAGTACAGCAATTGAGCTGATCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTATCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTGTTAC[A/T]GGCTAAAAGCTCTGGTTTCGACTGGGGGCAGAAATGTACAAGCAGCCTGTGACTGGTGAGTTTTGCATGTGCACACACACCCACACACAGACACGTATGCACATGAACCATGTTGTGCCCTGAGCCACACACACTCTCTCTGAGCTTTGAAATGGTAATGCGTTTTATTCTAGAATCATTACATTAGACCTGATCACTTATACAGATGAAATCAGCTTCACGTTGTAATGGTTTACTGCTGCCCTCTGGCGGTGGGGAATTGGAAATGTGTTTACAGCTGATCTGTTTAAGGGATGGTACACTCCAAAACGAAAAAGCTCCCAATATGTACACATCATTACATTTAACTGAGTGGTTATACGCCTTTATTGGTTTCTTTCTTCTGTTGAACACAAAAGAAGATATTTTGAAGCTGGAAACTTGTAACCATTGGCATTCAGACACTATAGAAGTGTCAGCTTTTCTCGAGAGGAAAGAAAGCCAAACAGGCTTGGATCAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11071
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 |
|---|---|---|---|---|---|
| ENSDART00000087128 | Nonsense | 339 | 599 | 7 | 13 |
| ENSDART00000143434 | Nonsense | 383 | 643 | 8 | 14 |
Genomic Location (Zv9):
Chromosome 5 (position 31529838)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 29291195 |
| GRCz11 | 5 | 29891348 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGCTGCGCCCCAATCAGTCTCTGTTGCCTAAGAGGACTCTGTTTGTGTG[T/A]CGCCATGGTGAAAGAATGGATGTAGTGTTTGGGAAACATTGGATCACTCA
Long Flanking Sequence:
TAATAAAATACAAGACCCTTAAGTATTTTGATACAAAATAATAAATCATTTTTATAAACCCTATGAAATATAAACGCAAAATACTATTTTGTATTTAAAATAAGTATTTAAAATACTTGTGTCATAAATGCTGCCCATCCCTGGCAGTAGTGACAGCATGATGAAAGCATTTACTGAAATGTTTACTCTTAACTAATGTCGATCAACTTTTTCAGGTCATTCTCTTTCCTTAATGGAACCCCCCCAACCAATATTAGGGGTGCAATGGGTGGGCTTTTTCTTGACCAGCACTTGGACGGTCGTCTTTTTGATGACCCTATGCCGCTGGATTCCCCCAATCTTAGTGTGATATGTCAGCCTATGCAGGTAGAACACTTAAGGAGAAATGCTGTCTTATTGTGAGTTTTCATGTGTGCTTTTATTCAAGCTATTATTTCTGATTCGTTATAGATGCTGCGCCCCAATCAGTCTCTGTTGCCTAAGAGGACTCTGTTTGTGTG[T/A]CGCCATGGTGAAAGAATGGATGTAGTGTTTGGGAAACATTGGATCACTCAGTGCTTTGATGCCAAAGGTCTGAGTTCAGCTTTTCAAATCAGTTCTTTAACTTCTTCCCATGACCAATAAAAGTTTTAAAAGTGAATCTTTATATTTAGCTCTGAGGAATTTCTTCAACTGTACACTCACTGGCCTCTTTATTAGGTCCTGCTAGGTTGCAGTTTGGACCTCACATTGCTTTCAGAATGCCTTAATTCTTTGTAGCTGGAAATATCCTGCTGATAATTTGATCCATATTTACATGATAGCATGATGCAGTTGGTGGCTGCACATGATGATATGAATCTCCTTTTCTAGACCTTCACAAAGGTGCTCTAGTGCAGTGTTTCTCAACCACTTTCCTGAAGGACCACCAGCTCTGCACATTTTCCATGTCTCCTTAACTGAACAGCCTGATTCAGATCATCAGCTCATTAGCAGAGACTGAAAGACCTGCAATGGGTGTGACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40459
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000087128 | Essential Splice Site | 362 | 599 | 8 | 13 |
| ENSDART00000143434 | Essential Splice Site | 406 | 643 | 9 | 14 |
Genomic Location (Zv9):
Chromosome 5 (position 31531947)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 29293304 |
| GRCz11 | 5 | 29893457 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTAATGTTTAATAGTTATAAATGAGTGTTCTTGTTTTGTTTATTGAGC[A/T]GGTCGATATGTGCGGTCAAACCTCAATATGCCTCTGAGTCTCCCAGCGAG
Long Flanking Sequence:
TTAGGGCAGTAGTTTCCATACTGTGATACCGTGAAACAGTGATGTTTATATCTAAGGTTATCATACCATCAGAATTTTATATCGGCCCATGCCTAGTCTTGACCACATCTACATGTCTAAATACATTGTTGTTGACATGTGATTAACTAATTAAAATTATTAAATATTTTGCATTAATACACAGTTAAACATGTACAGTTGTGCTTAAAATTTTAGCTATGTTTTTGTTTTGTGCTATATGTAAGCAAAAATATCTTGCTGAGAACAACATTAAATAAAAAAAATGACATACAGTTTGTTAGATCTCTCTCATTTAGTAAAAAATATTAACTTTTCAACGTATACTTCAAGGAGTATGTAAACTCTCGAGCACAACTGTATACCTAATAAAGTAAGTCGATAAAATGAAAGTAAAAATAAGGAAGTCATGAACATTCATTTTGAGAACCCTGTTAATGTTTAATAGTTATAAATGAGTGTTCTTGTTTTGTTTATTGAGC[A/T]GGTCGATATGTGCGGTCAAACCTCAATATGCCTCTGAGTCTCCCAGCGAGGAGTGGTGGGTATAGAGACTATGATAAAGACTGTCCTATCACTGTGTTTGGATCCACACAGGCTCGCCTAGTCGGTCAGTCCCACATCACTGTTAAATATGAATTTAGAGCTAAATTTATTTTCAAATTGCCAACAAACTTGTATTTACTTAATGTGTGCTATGCATTTCAGGGGAGGCTCTTTTTGAAAGTCACACAGTGGTGGACTTTGTATACTGTTCTCCATCTCTGCGCTGTGTGCAAACAGCACATAATATCCTCAGAGGTAAAAAACCTTTATTCTTTCATCTTTCTTTTTATTCCTTCAGGAATTAATTTGTACTTCATTAACCATGGCAGAGTTCACCGCTAAAGCAGTTTCTGCCCATGCTTCTTTATAAATCATGGACTTTCTGTCTTAGGTCTTCAGAAGGATGGCAAGACTAAGATCAGAGTTGAGCCAGGTTTGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6982
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 |
|---|---|---|---|---|---|
| ENSDART00000087128 | Nonsense | 457 | 599 | 10 | 13 |
| ENSDART00000143434 | Nonsense | 501 | 643 | 11 | 14 |
Genomic Location (Zv9):
Chromosome 5 (position 31532468)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 29293825 |
| GRCz11 | 5 | 29893978 |
KASP Assay ID:
554-5158.1 (used for ordering genotyping assays)
KASP Sequence:
GACTAAGATCAGAGTTGMGCCAGGTTTGTTTGAGTGGACTAAATGGGTGT[C/A]KGGTACCTCATTACCTGCCTGGATYCCTCCTACAGATCTGGCAGCTGCTA
Long Flanking Sequence:
CCTCAATATGCCTCTGAGTCTCCCAGCGAGGAGTGGTGGGTATAGAGACTATGATAAAGACTGTCCTATCACTGTGTTTGGATCCACACAGGCTCGCCTAGTCGGTCAGTCCCACATCACTGTTAAATATGAATTTAGAGCTAAATTTATTTTCAAATTGCCAACAAACTTGTATTTACTTAATGTGTGCTATGCATTTCAGGGGAGGCTCTTTTTGAAAGTCACACAGTGGTGGACTTTGTATACTGTTCTCCATCTCTGCGCTGTGTGCAAACAGCACATAATATCCTCAGAGGTAAAAAACCTTTATTCTTTCATCTTTCTTTTTATTCCTTCAGGAATTAATTTGTACTTCATTAACCATGGCAGAGTTCACCGCTAAAGCAGTTTCTGCCCATGCTTCTTTATAAATCATGGACTTTCTGTCTTAGGTCTTCAGAAGGATGGCAAGACTAAGATCAGAGTTGAGCCAGGTTTGTTTGAGTGGACTAAATGGGTGT[C/A]GGGTACCTCATTACCTGCCTGGATTCCTCCTACAGATCTGGCAGCTGCTAACCTTAGTGTGGATACAACATACAGGTATGTTATTATACATTCCCTGTGCTATATATCCTTTTTTGCTACAATATTTGATTGTACTTTTGCTTATTGATAGTGTTATCGGTTGTCTACATTTGTTTTCCTAAGCAACTTCCTGCATTAAATGGACATTTTATTTATTATCAAGTTGTCTTGTTCCTCTCCAGACCTCATATACCCATCAGTAAACTGACTGTGTCTGAATCTTATGAAACTTACATCAGTCGCAGCTTCCAAGTGACTCGTGAAATACTGTCGGAGTGCAATAATCTGGGTAGGTCATCGGTGTGGGTACTTTTGCAGATTTGTTATCTAAATCTATGCTCATCTGAATGTTGTATGCTTTGCGAAGCTCTCTGTTTTTTATAAACTGTTGTTCTGATGTCAAACAGGAAATACAGTGCTGATTGTGGCCCATGCTTCCT
Associated Phenotype:
Not determined