ZMP
UBR3 (1 of 2)
Ensembl ID:
Description:
ubiquitin protein ligase E3 component n-recognin 3 (putative) [Source:HGNC Symbol;Acc:30467]
Human Orthologue:
UBR3
Human Description:
ubiquitin protein ligase E3 component n-recognin 3 (putative) [Source:HGNC Symbol;Acc:30467]
Mouse Orthologue:
Ubr3
Mouse Description:
ubiquitin protein ligase E3 component n-recognin 3 Gene [Source:MGI Symbol;Acc:MGI:1861100]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa16777 | Nonsense | Available for shipment | Available now |
sa31698 | Essential Splice Site | Available for shipment | Available now |
sa41342 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa41341 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa16777
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 |
---|---|---|---|---|---|
ENSDART00000123038 | Nonsense | 79 | 347 | 2 | 8 |
Genomic Location (Zv9):
Chromosome 9 (position 4019469)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 4035848 |
GRCz11 | 9 | 4004819 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCATGTCTGAAATGGTGCTGCCGCGGTTTATCATCACTATCATTCAATA[T/G]CTGAGAGACGGCTACACTGAACCAGGTGAGGACACCAGGGGCTTTATTTT
Long Flanking Sequence:
TCATCAGTAGTGTAATTGTCAATGTATTCGCTGTGCAGGAATGGGGATATTGGCACATTTATTTCTGGAGTGTGTTTAGTGTTAAAAAAACCCACTTTGGCACTTGCATTTCATCACTCGTGTGTTCTTATGACTGACAGCATGGACTGTTTGTCTGAGCCGACTAGTCCATGATCTTACTGATACCCTGATGGCGGTCGCTTGTGCGTTAATCTGTTGACATTTATGACGAAGTTCTCTGACCACAGACATCAAATAGATGCTCGTAAAATTTTTATGTAGCCACGGTTGTTTTTTAAATATAAGGTTTTGTTTATTACAATACATTTTTACGGTAAGCTACTGACGTTATATAACCAACTGTATTATTTGTTTTTGTGTGACAGGTTTTGTAACAGACATCGATTAAAAACAGGAGAGAACGTTCCATCAGTCCCTCGAGATCTGCTGCTCATGTCTGAAATGGTGCTGCCGCGGTTTATCATCACTATCATTCAATA[T/G]CTGAGAGACGGCTACACTGAACCAGGTGAGGACACCAGGGGCTTTATTTTGACGGTCCATGCGCAGAGCGCAAAACGCAGGGCGCAAACGCTTTCAGGGTGTGTCAGAACACATCTTTGCTAATTTAAGGACGGGAAAAAAGGCGCATGGTCTACAAGGGTTGAGTTTATTTTCTTAATGACATATAGGTGTGTTTTGAGAATAAACCAATTAGAGTCTCATCTCCCATTCCCTTTAAGAGCCAGCTGTGTCGCGCCATAAGCGCATTCGCTATTTACAGGACGCAAAATAAGTCTAAGTGGAAAAACTGAGCATTTCACACGCATACAGTTAACAGAAAACTGTTAAACAGAGCATCTACTGCGTGAGAATGAGAGATAATGGATCTACTTTCACTTTCGCTCTTGGATAGGGAAACCTTTAAGCACAGACATCAATTAGACTATAAATAATTAATTGCGTTTGTTAAACGCAAATATTAGTTTCTAAACTATTTCTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31698
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000123038 | Essential Splice Site | 142 | 347 | 3 | 8 |
Genomic Location (Zv9):
Chromosome 9 (position 4017787)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 4034166 |
GRCz11 | 9 | 4003152 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTCACCAAGATCTTAACCGATCAGCAGACCTTTAAAGAGCTCAGCATGG[G/A]TATGTATGGGATGTGTTGGCATTGCAACATTTATTTATATTTATATTGTT
Long Flanking Sequence:
GCCTTGCGCCACATTGCGCCGGGTGTATGATAGGGCCCCAGATCACAACTTAAAGGAGTCTGTTGTCCAAAAAATTAAAGTTCTGCTATCATTTACTCACCCTTTACTTGTTCAAAACCTATTTGAGGTTCTTCCATTAGACACACAAGATATTTTGAAAATGCTTAATAGGAAGGCGAATAATTTTTACTTTAACTGTGCATTAGTTAATGGTCATATTGAGAAACATTCGTGTCTATGAACAAAGGGATGGGTTAAATTTTATGACTTTATGACTAACTGTTGTGAGACTGGCTTTTCGAAAATTATTTTGTTCAACACGTTAACTTGTTCTGATTTCCTGGCAGAGTCGGCCGCTGACAGAGATCTTCAGAAGGTTCTGCAGCAGTTGGATCCACACATCTCCTTCTTAGAAGAGCTCACCAAGATGGGCGGAGCCATGCGCACCGTTCTCACCAAGATCTTAACCGATCAGCAGACCTTTAAAGAGCTCAGCATGG[G/A]TATGTATGGGATGTGTTGGCATTGCAACATTTATTTATATTTATATTGTTTATCTAATTTCCAAGAACTGTTTCCAGTCATTGAGACTCGATATTTGCACACGTTTTTCGTATGTATGCGCACGTTTGAACTTCTCACAAAAACTTTCTACCTAATTCTCAAGTGGGTATTTGCATGAGTTAGACTTCTTCTTCTTTTAATGATTTTAGAGTTTTTTAAATGAAAACCAATGTGTACAAGGTTATTAATTTGCAGAATACATGCCCAAACTTACTCCATATAGGGGCTTTCCACAAATCGTTACTTGACCAGAGAAAGATTATTATGGTGCCAAAAACTAAAGACAAAGAAAAAGGCCTTTAACAATAATGAACAACAAGTTTTGTTGTCAGAGTTTAAAGCCAGAAAAAAATGTGCTAGTTAATATCCATTTATATTAATAAAACTTTAATTAAACTTTTATTATCAATTAGTTACTTTGAAATAGCATCTGATTATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41342
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 |
---|---|---|---|---|---|
ENSDART00000123038 | Essential Splice Site | 226 | 347 | 7 | 8 |
Genomic Location (Zv9):
Chromosome 9 (position 4014082)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 4030461 |
GRCz11 | 9 | 3999205 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCTCTTTATATCTAAAATTTCTTGGTTTTCTTGCTGTTTCTGTTTCGAT[A/T]GATCCATCCATAATGGACACGCTGAAACATAAATGCTTTTTAGAAGAGTT
Long Flanking Sequence:
CAGACTTTAAAGGAATAAACAATGTGGGGAAAGCTCCATTATAGTGCACTGGACAGGCAGTTCTGTACAATTACGTAATTTATCTGCTTAAAGATATCAGACTTAATTTAGACATCAGACCGATAACGATAATCTTAAATATATCATAATAAGTTACTATATCCTAATATATCGGCCGATATATCGTCCTAAAAATATATTGTTTTCAATTGGCTACAGAACACCTGTTGTCCAGTAACTTGCCTAATTAACATCGTTAATCTAGTTTAATATGGCACTTTAAGCTAAATACTAAAGTCTTGGATAATAACCAGAAAAATATAATTTGCTGTCATAGCAAAGACTAATGGAATTTGTTGTTCAAAAGTTAAAATACCACAGGAGGGCTATTAAGTTTTACTTCAGAACTTGAAATAATTTCTCAAATAAAATAAACATGCATTGATGTCTTTCTCTTTATATCTAAAATTTCTTGGTTTTCTTGCTGTTTCTGTTTCGAT[A/T]GATCCATCCATAATGGACACGCTGAAACATAAATGCTTTTTAGAAGAGTTACTGTTTTGGACTATTAAGTATGAATTTCCACAGAAGATGGTGACGTTTTTGCTCAACATGTTGCCAGATCAGGATTACAAGGTATTTAATTCTATTTTAAGCATATTTCAGTCTATATGTGCAGGATTCAAAATTAACTTGTGGTTTGTTGAATCTGTAAATTGCTAAATCTAGCCAATTTTGGTACATTATTTGATTTTGAGAATGAACATTGCTAGTAGTTTTCAAGCAGTCATAAGCAGGGCCACATGGAATCTGCAGACATTTTTTGCTATTACTGCACGGAATTTTGATAAAAATTTACAGATTCATGCGGAATGATTTTGGGGGTATCATAACTAAAATATTCTATTTATATTATATTAATATTCCTTAATATATGATCTAAAAAGGAATACACTTTTAACTTGTATTTAGTGTTTACAATGCAAATCCAATTAGATCCACTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41341
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 |
---|---|---|---|---|---|
ENSDART00000123038 | Nonsense | 253 | 347 | 7 | 8 |
Genomic Location (Zv9):
Chromosome 9 (position 4014000)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 4030379 |
GRCz11 | 9 | 3999123 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATGCTTTTTAGAAGAGTTACTGTTTTGGACTATTAAGTATGAATTTCCA[C/T]AGAAGATGGTGACGTTTTTGCTCAACATGTTGCCAGATCAGGATTACAAG
Long Flanking Sequence:
TCTGCTTAAAGATATCAGACTTAATTTAGACATCAGACCGATAACGATAATCTTAAATATATCATAATAAGTTACTATATCCTAATATATCGGCCGATATATCGTCCTAAAAATATATTGTTTTCAATTGGCTACAGAACACCTGTTGTCCAGTAACTTGCCTAATTAACATCGTTAATCTAGTTTAATATGGCACTTTAAGCTAAATACTAAAGTCTTGGATAATAACCAGAAAAATATAATTTGCTGTCATAGCAAAGACTAATGGAATTTGTTGTTCAAAAGTTAAAATACCACAGGAGGGCTATTAAGTTTTACTTCAGAACTTGAAATAATTTCTCAAATAAAATAAACATGCATTGATGTCTTTCTCTTTATATCTAAAATTTCTTGGTTTTCTTGCTGTTTCTGTTTCGATAGATCCATCCATAATGGACACGCTGAAACATAAATGCTTTTTAGAAGAGTTACTGTTTTGGACTATTAAGTATGAATTTCCA[C/T]AGAAGATGGTGACGTTTTTGCTCAACATGTTGCCAGATCAGGATTACAAGGTATTTAATTCTATTTTAAGCATATTTCAGTCTATATGTGCAGGATTCAAAATTAACTTGTGGTTTGTTGAATCTGTAAATTGCTAAATCTAGCCAATTTTGGTACATTATTTGATTTTGAGAATGAACATTGCTAGTAGTTTTCAAGCAGTCATAAGCAGGGCCACATGGAATCTGCAGACATTTTTTGCTATTACTGCACGGAATTTTGATAAAAATTTACAGATTCATGCGGAATGATTTTGGGGGTATCATAACTAAAATATTCTATTTATATTATATTAATATTCCTTAATATATGATCTAAAAAGGAATACACTTTTAACTTGTATTTAGTGTTTACAATGCAAATCCAATTAGATCCACTTTATTTTGTAAACAAAGCAAGTCTTCTATATAATATGTCTACTAAATGTGACAAAAAATGACTTTATATACTGTATTGTGAAT
Associated Phenotype:
Not determined