ZMP
ube3b
Ensembl ID:
ZFIN ID:
Description:
ubiquitin-protein ligase E3B [Source:RefSeq peptide;Acc:NP_001108154]
Human Orthologues:
HECTD3, UBE3B
Human Descriptions:
HECT domain containing 3 [Source:HGNC Symbol;Acc:26117]
ubiquitin protein ligase E3B [Source:HGNC Symbol;Acc:13478]
ubiquitin protein ligase E3B [Source:HGNC Symbol;Acc:13478]
Mouse Orthologues:
Hectd3, Ube3b
Mouse Descriptions:
HECT domain containing 3 Gene [Source:MGI Symbol;Acc:MGI:1923858]
ubiquitin protein ligase E3B Gene [Source:MGI Symbol;Acc:MGI:1891295]
ubiquitin protein ligase E3B Gene [Source:MGI Symbol;Acc:MGI:1891295]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa33564 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa33565 | Essential Splice Site | Available for shipment | Available now |
sa25293 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa20376 | Essential Splice Site | Available for shipment | Available now |
sa7558 | Missense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa33564
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 |
---|---|---|---|---|---|
ENSDART00000088968 | Essential Splice Site | 209 | 1069 | 6 | 25 |
Genomic Location (Zv9):
Chromosome 5 (position 21234951)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 18947823 |
GRCz11 | 5 | 19451623 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAACATCATGGGACATCTAAATCAAAAGGGCTTCTACTCTGTTCTTCAGG[T/C]ACTGTTTATCCAGACAGCCAGTCTTATTTTTACCACAGAATAGGCATGGG
Long Flanking Sequence:
CAAAAATGTAACAAGTAATCCACATATAAACCAGCCTGTGAGCTTTGATAGACAGCATAGACAGGGCAGCTTTTTTAGGCTTTTTTACAAACACATCACACATTGGCAACTTAATAATAATGATAACAAATAAATAATAAATGAGATTCTTTAGTTCTGAATCTGTTCATACAACCCAGAATGTGCTTCTTGTTAAATTCTTACTTCCTGTTTTCCTTTTCTCTCACCAGCCTGACATTCTGCAAGATAACAAATTGGTGACACTGTACTTGACAATGTTGATTACCTTCACCGACACATCGACATGGAAAATCATCCGAGGGAAGGGTTCGTATCACATGTAATCGGAGATAGTGATTTACAGGTTAAAATGCATAGAGCCTACTTGAATTTCTTGTCTTTCTTTTCTGAAGGAGAAGCCCTTAAGCCTGCTTTAAACAGGATTTGTGAGAACATCATGGGACATCTAAATCAAAAGGGCTTCTACTCTGTTCTTCAGG[T/C]ACTGTTTATCCAGACAGCCAGTCTTATTTTTACCACAGAATAGGCATGGGCCGGTATATGATTCTGACGGTATGATAACCTTGGATAAAAATATCATGGTATTACAAGATGGTGATTACTGTTCTAAAATATATTCTTTTTAAATGTCTGGGTAAAAAAACAAAAACAAATTTCCCCTTTGAACGTGATATATTTCATTTTGAGAGATGTTTAAAATATTTTGGAGCAGTAAACATGTCAGGCTAAATAATTAAAATGAATCATCTTGTCTTCATTTGTTTCAAAAACACAGATTTCTTTATAATTTAAAACAGCATCTTTGGAAATATTTTTTGCTGGATATACTCTTGTCCTAAAAAAAACTAAAAGTAAAAAATATATACATACACCGTAGGAATGGTACAGCAGAAAATGTTGGTGGTTTTAAAACCTTGATTTTTCCAAACCACGGTATACCTTGAAAACGGTTATCATCCAATACCTACTACAGTCTGTCAGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33565
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000088968 | Essential Splice Site | 429 | 1069 | 12 | 25 |
Genomic Location (Zv9):
Chromosome 5 (position 21242424)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 18955296 |
GRCz11 | 5 | 19459096 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTTGTCCTGATTTCAATGAGGAACTTTTGTTGAACTCCCTGCACGATTA[G/T]ATCTGTTCAAGCGAGCATTCCAGAAATCTGCTTCTGTGCGGAACATCCTG
Long Flanking Sequence:
TAGAACTTGGTGATGACGTCTTAATATTCTGGGAAGGTCCTTAAAAAGTCTTAAAAAGGTATGGAAATTTCCTTTAGGATTCCTGCATATACCCTGATATAGCATGAAGCTAATTTGCAGGCCTCCTCCCTGGTTAGGCTATCACATAAAAAAAATAATAATAATAATAAAAAATAAAATAAATAAATAAATCCATTATATAGGATGTTTTTTTTTTATTCGCTTTGCAAAAATCAACAAATAAAATGTTTTTTTTTTTTTTTTTTTAATCTTTAAAAATCACATAGTGAATGCTTAGCAGGACTGGCTGTATTTTATTTTTCACAGTATGGTCTGGACTAAATGAATCAAGAGAACTGAACTTTAAGTTTGGACACATTTTTAGTATTTCAGTTTTCCTCAAGGAATAAATGTGAACAGAACAAATAAAACAGTAGTGTGCTACTCTGAATTTGTCCTGATTTCAATGAGGAACTTTTGTTGAACTCCCTGCACGATTA[G/T]ATCTGTTCAAGCGAGCATTCCAGAAATCTGCTTCTGTGCGGAACATCCTGAAGCCGGTCGGGGGGAAGCGTGTGGACTCTGCTGAGGTCCAGAAGGTGTGTAGTATCTGTGTGCTGTATCAGACGGCCCTCACCACACTCACACAAATCCGTCTGCAGATTCTCACAGGTACGTGCTTTTCTTATTTACATTTAAATCATGCACATTCAGACATTTTAGTTTAACCTCTTTTTATTGCATTTTGTCTGAGCTTATAGTTCATGCTATTGTTTCAGCAGTTCATCTCACCACATTTTAAGATTCTTGATTTATTCTGCACATTTGCAGAATAATAGTTGTTTGTGGGATAGAATAATTATTTTATATCATAATAACTTTGAATAATATTGTAGTTAATCTCGACTCAGCAGTTTCCAATTTAAACTCTGTTTGCAGGACTGACATATCTGGATGAATTGCTGCCTAAGCTGTGGGCATTTATCTGTGAGCTCGGCCCTCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25293
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 |
---|---|---|---|---|---|
ENSDART00000088968 | Essential Splice Site | 620 | 1069 | 15 | 25 |
Genomic Location (Zv9):
Chromosome 5 (position 21245024)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 18957896 |
GRCz11 | 5 | 19461696 |
KASP Assay ID:
554-7606.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGAGGGACTGTCGCAGGAGATTCACGCCTGAAGATCACTGGCTCCGCAA[G/A]TATGCCGCCCTCACATTATCACTGAGCCACATTACTCTGCTGATTTACTT
Long Flanking Sequence:
TGATGCTGAACATTGTTTATAATTAAAAATATGATCAAACTATTACCAAATTGTCTGTTTTTACATTTGTGTGTTTTGCTGTTACAGTATTCTGGATGACATTGAGGTGTACGAGGAACAGATTTCTTTCAAAATGGAAGAGCTTGTCACGATCTCCTCATTCCTTAACACATTTGTATATAAGATGGTCTGGGATGGTATTTTAGGTAGGTGTTATTTAGTTTTTACAACAAGTAGTTTTTTTATGCATTAGTTTCTCCATTCTTGTTCTCCAGTCTTTACTTATGCTTGCAGCCTCATGTAGATAAAGCTTGGTTGTTTGAACCATCTGCATATGGAGCTGGTGATAACGTGCTGTTCTCGTGTGGTCATTAATTCGTTTTAGAGAACGCCAAAGGGGAGAAGTTGGACTTATTCCACAGTGTTCACGGCTGGCTGATGGTTTTGTACGAGAGGGACTGTCGCAGGAGATTCACGCCTGAAGATCACTGGCTCCGCAA[G/A]TATGCCGCCCTCACATTATCACTGAGCCACATTACTCTGCTGATTTACTTTAGAGTTCAGGTCCACTCAAATGAAATAAATTGCTGCTTGTTATATTCCTGTAGGGGAAAGCTAAATGTATCGACCTACAAAATAAGTCTCATTTGTTTTCTTTTTCACTGTGTGTCGAATACAGGGACCTGAAGCCCAGCCTACTGTTCCAAGAGCTGGAGAAAGGCAAAAAGAGAGCGCAGCTGCTGCTTCAGTACATTCCTCATGTCATCCCACATAAAAATGTGAGAATAAATCTCCAGAGATTATCAATGTTTTAGTTGATTGCATCAATTGAGGATTTAATCTGGATTTAATGAGATGTAGAACATAATTTACATTTAATAAAGGAGAAAATCTTCTTTATTTTTTAAAGTTAAGATCAATATTTACTCTTCTTAATTTTATACAGTTGAGTCAGAGTTATTAGCCCTCCTGAATTATAAGCCCCCCTGTATATTTTGTTCCCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20376
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000088968 | Essential Splice Site | 835 | 1069 | 19 | 25 |
Genomic Location (Zv9):
Chromosome 5 (position 21248891)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 18961763 |
GRCz11 | 5 | 19465563 |
KASP Assay ID:
2259-5608.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTGCCCTCGCTCGACTCCGAGTTTTACAAAAACCTCACCTCCATTAAGG[T/G]CAGTAATAATGCGACTACTACAAAGAAAGTTTGGGAAATGCTTGATTTTG
Long Flanking Sequence:
AGAAGCAAGTTAGATCATTTGTATTTTTACCTTGTATTGCTGCTATAAATACAACTCTTCATTTGCTCTCTAAGTATGTTATGTAGTTCTCAACACATTGCTGTTATTTTCTCTTTAAAATAGTTTTCCCTTAATCTTTTTCAGTTAAAAAGCTCATTATAAAGTCTTTTACCCTCATAAAACCTGCAGACACCTTGGTGCTTACTTCGCCAATAAACCTAAACCACTTAATTGTTTTTGTCTCTTTCAGACCACCAGTGGGAATGAGAGATTATACCCCTCCCCAACCTCCAGCATCCATGAGAACCACCTTCAGCTGTTTGAATTTGTGGGGAAGATGCTGGGAAAGGCCATGTATGAAGGCATTGTGGTGGACGTGCCGTTTGCCTCTTTTTTCCTCAGTCAGGTTCTGGGTCACCATCACAGCACCTTCTATAGCTCCATAGATGAGCTGCCCTCGCTCGACTCCGAGTTTTACAAAAACCTCACCTCCATTAAGG[T/G]CAGTAATAATGCGACTACTACAAAGAAAGTTTGGGAAATGCTTGATTTTGATTTATGTTTTTAAGATATGTAATGTACTTGGATTTATATGTACTTGGATCTATAATATTTTTTTATCCAATGTGATTAAAAATTGTAAAATATTAGTGAAAAATAACCAGTTCAGTGCTTCCCACACAGACTTTACTTGGGCGGCTGCCCAGGTATATTAACGACCGCTCAATACATTCAGTGACACTTTTTTTTTGCTATTATTATCATACTGTTACACTTTTTTTTGTATCCACCCAACATAAACAAACATCCGCGAGAGATTAAGTATTGAAAAATCTTCTCTTCTTTACCTATTTCATACTACTTGTTCAGTGTGCGCTACCACAGGTAATCTCACATGCTCTGCAGACGCACAGAGACCCTCACCTTTTGGCGTCTGGCTGGGGTATCTACTGAAATGTCCAGGATTTGGTTTTGTTTTAATTTTCTAAGCTGTCGTTAATTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7558
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:
Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000088968 | Missense | 916 | 1069 | 22 | 25 |
Genomic Location (Zv9):
Chromosome 5 (position 21251204)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 18964076 |
GRCz11 | 5 | 19467876 |
KASP Assay ID:
554-4154.1 (used for ordering genotyping assays)
KASP Sequence:
ATTYATCAGGGGCTTTCGCAGCATCATCAAYCCAGAGTGGCTGCACATGT[T/G]TTCTACCCCGGAGGTCCAGAGGCKCATCTCGGGAGACAACGCTGARATAG
Long Flanking Sequence:
GGTGGAAAGACTATGCCTGTCACTAATGAAAACAAGTGAGTCCATTTTGTCTCTTCGGTCAACTGTAAATAAAATTTCCATGCCAGTGCAGCCCTCCTATTCACATTCAATGCAATAAGAAGAAATGACCCGATAAAAAAACTAATTAGTTTTGGATGCAGACCGGTTCAAAAAGCAATTATGGATTTGCAACCTCAGACAAATGCTTATTTATGTAAACCTGTTGTTTTCACTAATGGATTACCTTATATCTGTAACTCTAATAGGACTGAACAGAAGGTTTTTCAGTTCATGTTTTTTCTTTATGTAAAAAAAGTCAGCCTGGCTTAGCTTCTCTCTTTTTTTGTACATGTGTTAATCGTTATCCATCATTCTATCCTCCAGGATCAGCTATATCCACCTGATGGCCCATTTCCGCATGCACACTCAGATCAAGGAGCAGACGGCTGCATTCATCAGGGGCTTTCGCAGCATCATCAACCCAGAGTGGCTGCACATGT[T/G]TTCTACCCCGGAGGTCCAGAGGCTCATCTCGGGAGACAACGCTGAGATAGATCTGGATGATCTCAAGTAAGACCATGATTTTTAATTGGACTGTGTGATATTAACCAAAATATCATCTCAATATTTTTAAACATTTTCGCTAACAGGAATCAAGTTTGAGTTGATTGGGTTGAAATACATTTTGGTCTCCTCTGAGGTTGTCCGAATACCAATAATTTATCTTGAATAAAGAATAAAGGAACTTAAAACCTAAAAAGATGAAGAGTAAATAGTAGCGTTTTGGGGTAGTTCACCACATTCATATCTGTTGTGCAGATCTTTCCCCACAGATATCATAAAAGATAGTCCTAATAATCACATGCTGTGAACAACAGTCTTAAAAGGTTATTTATAATAGTGCCTGTAAAATTTTAAAATAAAAATAAAAATTCTTCTTCATTCTCTTTCAGAAAGCACACTGTGTACTATGGAGGTTTCCATAGCAGCCACAGAGTCATTCT
Associated Phenotype:
Not determined