ZMP
zgc:195004
Ensembl ID:
ZFIN ID:
Description:
ubiquitin associated and SH3 domain containing, B-like [Source:RefSeq peptide;Acc:NP_001122227]
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 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12056 | Nonsense | Available for shipment | Available now |
sa42534 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa17314 | Nonsense | Available for shipment | Available now |
sa42535 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa44823 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa42536 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa12056
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111213 | Nonsense | 79 | 642 | 3 | 14 |
Genomic Location (Zv9):
Chromosome 15 (position 20266133)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 21368759 |
GRCz11 | 15 | 21304491 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCTCTCATTTGGATGACCCGTTCCTRGATGACTCTTTACCCAGAGAGTA[T/G]GTGCTGTACCTGCGCCCCAGTGGRCCTTTACAAAACCAGCTTTCTCATTT
Long Flanking Sequence:
CCAAAAAATAAAAATAAAATAAATAAATAAATTCCAGATGTTCTTTACTTACTGATCTAATTCTTATATATCAAGGGAGATATTTTGGAAATGCAAGCCAGATGGGATTTAAACTTTGGTAAAGTTTGGTTTTAAAAGAAAAATGTATAATGCTGATTCACTAGTCCTGATTCTAACATTAACCCACAGCATTTGGTTTAGTTTTGTGGCTTTCATTGCAGAATAAAAAATTAGGTAATACTAAAAACCATCTATATACCGTTTCCTAAAAAAGCGATGGATTCATGAAAATGAAAATCTTACTTTTTTATTTACTCCAATTTCCCAAAATGCACTTTAATACAATGTCCAAAAATGGCCTATTCTATTAGTATATTCATAAACTATTCAAGTCAGCTTTTTAAAAAAAGACCCTGATTTATCATAATTTAAATGTGTCTCCATAGGCTTTTCTCTCATTTGGATGACCCGTTCCTAGATGACTCTTTACCCAGAGAGTA[T/G]GTGCTGTACCTGCGCCCCAGTGGACCTTTACAAAACCAGCTTTCTCATTTCTGGCAGCAGTCTCGCTTCACTTGTGGAAAGAACAAAGCTCACAACATATTTCCACACATCACGCTTTGCCAGTTCTTTATGGTGAGTCACACTTTCTATTTGAATCAGATAATCTGTCATGATTATGTTGCAGAATCTTACATGCTCTTACTTTGACGTGTTGTCCAGTGTCCAGACAGTAAACTAGTGGCTCTGTGTGAAGCTCTGCAGTCTTCTGTGAATCAGTGGAGAGGACGTTTCCCCAGCCCTTTGCCTCTGGAGCTCTACACCTCCACCAACTTCATCGGCCTGTTCGTGGAGGAGCAGGTGGCAGAGACGCTTAAGCAGTTTGCCGCGGACTTCGCGGTGGAGGCTGCTGCTAAAGTGGGTGAGGAGGCGTGAGCTGAGCTTTTCCACAGATGGTGCTCATGTTTTGTCTAATCGCCCCATTACTCACTTTGTTCCAAACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42534
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 |
---|---|---|---|---|---|
ENSDART00000111213 | Nonsense | 82 | 642 | 3 | 14 |
Genomic Location (Zv9):
Chromosome 15 (position 20266142)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 21368768 |
GRCz11 | 15 | 21304500 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGGATGACCCGTTCCTAGATGACTCTTTACCCAGAGAGTATGTGCTGTA[C/A]CTGCGCCCCAGTGGACCTTTACAAAACCAGCTTTCTCATTTCTGGCAGCA
Long Flanking Sequence:
AAAAATAAAATAAATAAATAAATTCCAGATGTTCTTTACTTACTGATCTAATTCTTATATATCAAGGGAGATATTTTGGAAATGCAAGCCAGATGGGATTTAAACTTTGGTAAAGTTTGGTTTTAAAAGAAAAATGTATAATGCTGATTCACTAGTCCTGATTCTAACATTAACCCACAGCATTTGGTTTAGTTTTGTGGCTTTCATTGCAGAATAAAAAATTAGGTAATACTAAAAACCATCTATATACCGTTTCCTAAAAAAGCGATGGATTCATGAAAATGAAAATCTTACTTTTTTATTTACTCCAATTTCCCAAAATGCACTTTAATACAATGTCCAAAAATGGCCTATTCTATTAGTATATTCATAAACTATTCAAGTCAGCTTTTTAAAAAAAGACCCTGATTTATCATAATTTAAATGTGTCTCCATAGGCTTTTCTCTCATTTGGATGACCCGTTCCTAGATGACTCTTTACCCAGAGAGTATGTGCTGTA[C/A]CTGCGCCCCAGTGGACCTTTACAAAACCAGCTTTCTCATTTCTGGCAGCAGTCTCGCTTCACTTGTGGAAAGAACAAAGCTCACAACATATTTCCACACATCACGCTTTGCCAGTTCTTTATGGTGAGTCACACTTTCTATTTGAATCAGATAATCTGTCATGATTATGTTGCAGAATCTTACATGCTCTTACTTTGACGTGTTGTCCAGTGTCCAGACAGTAAACTAGTGGCTCTGTGTGAAGCTCTGCAGTCTTCTGTGAATCAGTGGAGAGGACGTTTCCCCAGCCCTTTGCCTCTGGAGCTCTACACCTCCACCAACTTCATCGGCCTGTTCGTGGAGGAGCAGGTGGCAGAGACGCTTAAGCAGTTTGCCGCGGACTTCGCGGTGGAGGCTGCTGCTAAAGTGGGTGAGGAGGCGTGAGCTGAGCTTTTCCACAGATGGTGCTCATGTTTTGTCTAATCGCCCCATTACTCACTTTGTTCCAAACTGCATGACTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17314
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 |
---|---|---|---|---|---|
ENSDART00000111213 | Nonsense | 428 | 642 | 9 | 14 |
Genomic Location (Zv9):
Chromosome 15 (position 20278789)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 21381415 |
GRCz11 | 15 | 21317147 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGAATATGCCTGCAGCTCTGCCTGCTCGGGGTGCAACACATAGGGACTA[C/A]GAAATGGATGCTCCTATAACTGTGRTTGGATCCACACAGGCTAARATAGT
Long Flanking Sequence:
GAGGCGTTTCAAAGATGGCCACCGAGTGAAATAACTTGCCTTAAAAGGACGTTGTTTATAACTACTATTGAACAGTTATTATTTTAATAATAGACAGGGAATAAGCCTGCAGTTAATAGGATGAATTGTGACCTAATCTAGAGTGTTACTCAATAATTAAATGTGTATATATAAAAAAGGTCTGGTATTGTTTTTGTTACTTATAAATTGACATTTTTTGCTGTTGATGGTAGGTCCTTCGCTCTAACATCCAGTCTCGAGCTCCTAAAAGGACCCTGTTTGTATGTCGGCATGGAGAGAGAATGGATGTTGTTTTTGGGAAACACTGGCTCTCTCAGTGTTCTGACTCAAAAGGTAATCTCAACGGATGGGCCATGACTGTGCGCTCATATGGTGCAGTTAGTTTGTGAACTCACTTTGTCTCCTGTAGGCAGGTACGTGAGGAGGAACCTGAATATGCCTGCAGCTCTGCCTGCTCGGGGTGCAACACATAGGGACTA[C/A]GAAATGGATGCTCCTATAACTGTGGTTGGATCCACACAGGCTAAGATAGTGGGTAGGTCTGCTTAGTGTTTTGATGTTAACATGAGTTGACCAGTTGAATTGTCCATCATGCTTGTTTTATGTCATCTGATTTTCAGGGGAGGCTCTGCTGGAAAGTAATACCAGTATTGATTTTGTATATTGTTCACCCAGCCTTCGGTGTGTCCAGACGGCTCATGAAATTCTCAGAGGTATAGTACTGTAGTCAGGAATATGAAGGAAGCAGTGTGCGGGGGAAAGGATTGTTACTATGATATAAATAGGGTTGAATTTTCCTGTTGAGTTATGCTCTATGTTGGCCTGCATTTCAAAGAATTACACTTTAGTTTTTAATGAGCAGATTCAATTTGTTAAAGTTAGTACAGTATTCAAGTGTTTACAGTAGTTTAAGAAAAATAGCAAAACGATTAATTTTTCATAATAGGCTAATTTTATGTACAGAGAAATTTCTACACTGTAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42535
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111213 | Essential Splice Site | 445 | 642 | 9 | 14 |
Genomic Location (Zv9):
Chromosome 15 (position 20278842)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 21381468 |
GRCz11 | 15 | 21317200 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATGGATGCTCCTATAACTGTGGTTGGATCCACACAGGCTAAGATAGTGG[G/A]TAGGTCTGCTTAGTGTTTTGATGTTAACATGAGTTGACCAGTTGAATTGT
Long Flanking Sequence:
GTTTATAACTACTATTGAACAGTTATTATTTTAATAATAGACAGGGAATAAGCCTGCAGTTAATAGGATGAATTGTGACCTAATCTAGAGTGTTACTCAATAATTAAATGTGTATATATAAAAAAGGTCTGGTATTGTTTTTGTTACTTATAAATTGACATTTTTTGCTGTTGATGGTAGGTCCTTCGCTCTAACATCCAGTCTCGAGCTCCTAAAAGGACCCTGTTTGTATGTCGGCATGGAGAGAGAATGGATGTTGTTTTTGGGAAACACTGGCTCTCTCAGTGTTCTGACTCAAAAGGTAATCTCAACGGATGGGCCATGACTGTGCGCTCATATGGTGCAGTTAGTTTGTGAACTCACTTTGTCTCCTGTAGGCAGGTACGTGAGGAGGAACCTGAATATGCCTGCAGCTCTGCCTGCTCGGGGTGCAACACATAGGGACTACGAAATGGATGCTCCTATAACTGTGGTTGGATCCACACAGGCTAAGATAGTGG[G/A]TAGGTCTGCTTAGTGTTTTGATGTTAACATGAGTTGACCAGTTGAATTGTCCATCATGCTTGTTTTATGTCATCTGATTTTCAGGGGAGGCTCTGCTGGAAAGTAATACCAGTATTGATTTTGTATATTGTTCACCCAGCCTTCGGTGTGTCCAGACGGCTCATGAAATTCTCAGAGGTATAGTACTGTAGTCAGGAATATGAAGGAAGCAGTGTGCGGGGGAAAGGATTGTTACTATGATATAAATAGGGTTGAATTTTCCTGTTGAGTTATGCTCTATGTTGGCCTGCATTTCAAAGAATTACACTTTAGTTTTTAATGAGCAGATTCAATTTGTTAAAGTTAGTACAGTATTCAAGTGTTTACAGTAGTTTAAGAAAAATAGCAAAACGATTAATTTTTCATAATAGGCTAATTTTATGTACAGAGAAATTTCTACACTGTAAAGTGTAGGGCAAAAATTCTACTGTTCAACATTTGCTTTTCCACATCCAAACACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44823
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111213 | Nonsense | 537 | 642 | 12 | 14 |
Genomic Location (Zv9):
Chromosome 15 (position 20281502)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 21384128 |
GRCz11 | 15 | 21319860 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTTGCATTTCCACAGACCTCACATGCCCATCAGCAAACTAACTGTCTCC[G/T]AGGCGTATGAAACATACATTAGTCGCAGCAACCAGGTGACCAAAGACATT
Long Flanking Sequence:
AAAATAAGTGCAAGCTCCTCAAAATTTGGCACTATTTGTTTATATCTGCATTCAATTCTGTAATTGTAGAATCGCTAAATTCTGGAGGGACTGCACAATACATTTGCTGCTCAGAAGTGCCTTATATGTTAACTTGTATGTTAAAATATATTTCAAATACAGAAAAGGCCATACTTTTGAGCTTTATAATCAAAGAATTCTGAAGAAAAGTCACCCCAGTGTCTTTGCCCCTTTCTCTAGGAATGCAGCAAGAAGGCAGACTAAGCATTCGAGTGGAGCCTGGGCTGTTTGAGTGGACTAAATGGGTGTCAGGAACATCTTTGCCTGCTTGGATACCCCCTACAGATCTTGCTGCAGCCAATCTTAATGTGGACACAACTTACAGGTAAAAACAAAGTTATCATAGACTTTTTTGTGTAGGAGCATATGTCCAGTTCTGTCCTTATTCACAGTTGCATTTCCACAGACCTCACATGCCCATCAGCAAACTAACTGTCTCC[G/T]AGGCGTATGAAACATACATTAGTCGCAGCAACCAGGTGACCAAAGACATTTTGGCCTACTGCAAAAATAAGGGTAAGTGATTATAAATGCTGCTTCAACTCAAGTGCTTATGATTCTCTCTCACATGTACTAATAGTGGATCTTTTTTTACAACAGGTAAAAATATTCTGTTTGTGGGACATGCTTCCTCTTTGGAGGCCTGCACTCGCCAACTCCAGGGTCTTTCTTCACAGAATTCTAAAGACTTTGTGCAAGTAGTCCGTAAGGTTAGCTTCACCCTTTTTAAACATTTTACAGGCAGATCAATCTCATCAAATACTGCCAGGATATGTGACATCCTATGTAAAAGTACCCAGCTAAAAAAATGTGATTCATTGTTTTGCACATAAAATCATTAAAAGATGGACTTTTCAAAGCTGGTCTTTCCGTCCAGATTCCATACCTGGGTTTGTGTGCCTGTGAGGAGCAAGGGGACTCAGGAATCTGGCAGCTTGTGGATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42536
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 |
---|---|---|---|---|---|
ENSDART00000111213 | Nonsense | 554 | 642 | 12 | 14 |
Genomic Location (Zv9):
Chromosome 15 (position 20281554)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 21384180 |
GRCz11 | 15 | 21319912 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCGTATGAAACATACATTAGTCGCAGCAACCAGGTGACCAAAGACATTT[T/A]GGCCTACTGCAAAAATAAGGGTAAGTGATTATAAATGCTGCTTCAACTCA
Long Flanking Sequence:
CAATTCTGTAATTGTAGAATCGCTAAATTCTGGAGGGACTGCACAATACATTTGCTGCTCAGAAGTGCCTTATATGTTAACTTGTATGTTAAAATATATTTCAAATACAGAAAAGGCCATACTTTTGAGCTTTATAATCAAAGAATTCTGAAGAAAAGTCACCCCAGTGTCTTTGCCCCTTTCTCTAGGAATGCAGCAAGAAGGCAGACTAAGCATTCGAGTGGAGCCTGGGCTGTTTGAGTGGACTAAATGGGTGTCAGGAACATCTTTGCCTGCTTGGATACCCCCTACAGATCTTGCTGCAGCCAATCTTAATGTGGACACAACTTACAGGTAAAAACAAAGTTATCATAGACTTTTTTGTGTAGGAGCATATGTCCAGTTCTGTCCTTATTCACAGTTGCATTTCCACAGACCTCACATGCCCATCAGCAAACTAACTGTCTCCGAGGCGTATGAAACATACATTAGTCGCAGCAACCAGGTGACCAAAGACATTT[T/A]GGCCTACTGCAAAAATAAGGGTAAGTGATTATAAATGCTGCTTCAACTCAAGTGCTTATGATTCTCTCTCACATGTACTAATAGTGGATCTTTTTTTACAACAGGTAAAAATATTCTGTTTGTGGGACATGCTTCCTCTTTGGAGGCCTGCACTCGCCAACTCCAGGGTCTTTCTTCACAGAATTCTAAAGACTTTGTGCAAGTAGTCCGTAAGGTTAGCTTCACCCTTTTTAAACATTTTACAGGCAGATCAATCTCATCAAATACTGCCAGGATATGTGACATCCTATGTAAAAGTACCCAGCTAAAAAAATGTGATTCATTGTTTTGCACATAAAATCATTAAAAGATGGACTTTTCAAAGCTGGTCTTTCCGTCCAGATTCCATACCTGGGTTTGTGTGCCTGTGAGGAGCAAGGGGACTCAGGAATCTGGCAGCTTGTGGATCCACCAATTCTTCCCTTGACTCATGGGCCGAACCACAGCTTCAGCTGGAGAGA
Associated Phenotype:
Not determined