Busch Lab

ZMP

ubr3

Ensembl ID:
ENSDARG00000042508
ZFIN ID:
ZDB-GENE-030131-1473
Description:
Ubr3 protein [Source:UniProtKB/TrEMBL;Acc:Q1JPS8]
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 5 alleles of this gene:

Allele Name Consequence Status Availability
sa17047 Nonsense Available for shipment Available now
sa16003 Nonsense Available for shipment Available now
sa34547 Nonsense Mutation detected in F1 DNA Not yet available
sa10176 Essential Splice Site Available for shipment Available now
sa2488 Nonsense F2 line generated Not yet available

Mutation Details

Allele Name:
sa17047
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
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Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000047723 Nonsense 196 288 5 6
ENSDART00000062336 Nonsense 97 607 3 14
ENSDART00000129091 Nonsense 444 954 8 20
ENSDART00000129693 Nonsense 97 607 3 15

The following transcripts of ENSDARG00000042508 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 9 (position 3944302)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 3960681
GRCz11 9 3932210
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTCCGCTTTGCCGCCAGTTTGCAAACAGTGTTTTACCTTGTCGTCCTGGA[C/T]GAGGGATGGAAACCGGAGCCTGGCAYGCACCCAGTACCAAGAGCATGTCT
Long Flanking Sequence:
GCATAGTCTCTGGGAACCTCGGGATGAGTATCTCCAGGTGGAAATAAAGAATAAAGAGAATAATTAGCGTAGCTGCTGTTCACAAACATGACCTCCGTACAGAAATTTTAAGTATGGAGCAATCACTGCTTTTTTTAATGTCTAATCATCTTGTTTAATCTCACCTCTTTTCGCAGCGCTGTACTACAGAATTCTACAAGCTCAAACTCTAGTGTGACCATGGCATGAGAACAGAAAAAAACAACAGTATAGAGCAGACTGAATGCTTTATGAATAGTCAGTGAGACATTAGCCAATCATGACAAAAAGGATACTGTATCACCTGTTTTTGAGAACTAGTCAGCCATTAAACTTCATTAAATCAACCATTACCGAACCTGTTGTATTTGCTTGTTTTGCAGAATGATCAGGTTCTTCAGGGGATTTCTGTGGATAAAGGCGAGTTCACTTGTCCGCTTTGCCGCCAGTTTGCAAACAGTGTTTTACCTTGTCGTCCTGGA[C/T]GAGGGATGGAAACCGGAGCCTGGCACGCACCCAGTACCAAGAGCATGTCTACACTGGTGAAAGAAGTAGAAGACCTCCAGGAGCAGCTGGGCATTTTCCCAGTAAGAGCCAGCATAAAGCAAAGAGATCCCATTCTGGTATTTATTAGAGTGCTCCCCATCCCCTCTTTTCTGTTCTTTCCATCTCATCCCTCCATTCTGATTCAGAGTAAGAGCTGGTGCCACACTGACCTTCATGTGATCTTTCATGCCCCATCTAACATTGCTGTGGTTTAACTTCTCATAATGCAAAGACTCAAGTTGGTGTCATATATGCATGTCAAACATTAGTGAGGTACTGAATTTTCTGTCACTGAAACTGAAAGACAAAAATAGCCATAAATAAGTGTATGAGCCAAATTGTGTCCCTTTCAGTTTGCTGGTTTTGCTCTCCCTGCACTGTGAGAAGCGGCTTTCACACTGGACAAACAAAGCACTGCGCTATGAAACCCGTTCATTTCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16003
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000047723 None None 288 None 6
ENSDART00000062336 Nonsense 224 607 6 14
ENSDART00000129091 Nonsense 571 954 11 20
ENSDART00000129693 Nonsense 224 607 6 15

The following transcripts of ENSDARG00000042508 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 9 (position 3933145)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 3949524
GRCz11 9 3921053
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTCACGTGCTGGCCATGCACATGCGGCTCTACAGCATAGACTCGGCATA[C/A]AATCCATGGACCAGACTCACACTGAGCACGCAAAGCAGAGAGAATGAGTG
Long Flanking Sequence:
ATTGAAATGAGTTAATCTTACAAGCACCAAACTTTAACTTGTGGAAGTTTATGTACAGCAAAAAATGCAAGATACTTTAGCATTGTTCATCTCTTGGGTGTCATTCTTGAAAACGGTGGTCATTTTGCAGAATTCCTTTAGTTTTGTTTCCAGCAGCAGATCTGTCATTCCTCCTCAGACCGAGTGTTGTGATATGTGTGTGTAAAGTGTGTGTTGGTCTGCTGGTTTTGTGAGCTCAAGGGGGCAGCAGTGATCCATGACTCTCAGCCCTCTCCTAAAGACACCGCTCAGCATGTAAAAGGACACGAGCTCTGATATCTGTCATGTCCTCCTACACGCCTGGAGGCTTTACGCAAACTCCATTTATCATGTTTCACACTCTGACACTTGTGTGTGTGTGTGTGTGTGTGTGTGTAATGTGTATGTGTTCTCTGTGTTTCAGATCAGCTGTTTCACGTGCTGGCCATGCACATGCGGCTCTACAGCATAGACTCGGCATA[C/A]AATCCATGGACCAGACTCACACTGAGCACGCAAAGCAGAGAGAATGAGTGAGTGCGCTCGCGCACACACACACACACACACCCACACTTGTACAGTTATCTTTGTATGGACATCATCAGACATTAATTTTATACTCTAGAGACTGTATGCAGGGTTTGAAATGAACCATTTTGCTTGGTAGCACCGGTGCTCCCAACTTTAAAAATGTAGGCGCACCAGTCAAAATTTAGTCACACTCACCAATTATAAGCACCGTTACTACAAGTTTTATACAAACATATTCATTGCATTTGAAATCAACAGTAATCAAACTAACAAGCAAAATATATATGCAAGCGTGAGGAAAATATGTCTCAACGAAATCCCGTTATCACAAGAAAATAGATTTTTATAACATAACTGAGTGACCAAAGCATACACGGAGCGCTCACCGGCCCTGCACACACTGCTTGACATGAATGAATCTGTTAACGATATAACTGTGCTGTTCTCACGGGTGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34547
Status:
Mutation detected in F1 DNA
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
ENSDART00000047723 None None 288 None 6
ENSDART00000062336 Nonsense 238 607 6 14
ENSDART00000129091 Nonsense 585 954 11 20
ENSDART00000129693 Nonsense 238 607 6 15

The following transcripts of ENSDARG00000042508 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 9 (position 3933105)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 3949484
GRCz11 9 3921013
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTCGGCATACAATCCATGGACCAGACTCACACTGAGCACGCAAAGCAGA[G/T]AGAATGAGTGAGTGCGCTCGCGCACACACACACACACACACCCACACTTG
Long Flanking Sequence:
GTGGAAGTTTATGTACAGCAAAAAATGCAAGATACTTTAGCATTGTTCATCTCTTGGGTGTCATTCTTGAAAACGGTGGTCATTTTGCAGAATTCCTTTAGTTTTGTTTCCAGCAGCAGATCTGTCATTCCTCCTCAGACCGAGTGTTGTGATATGTGTGTGTAAAGTGTGTGTTGGTCTGCTGGTTTTGTGAGCTCAAGGGGGCAGCAGTGATCCATGACTCTCAGCCCTCTCCTAAAGACACCGCTCAGCATGTAAAAGGACACGAGCTCTGATATCTGTCATGTCCTCCTACACGCCTGGAGGCTTTACGCAAACTCCATTTATCATGTTTCACACTCTGACACTTGTGTGTGTGTGTGTGTGTGTGTGTGTAATGTGTATGTGTTCTCTGTGTTTCAGATCAGCTGTTTCACGTGCTGGCCATGCACATGCGGCTCTACAGCATAGACTCGGCATACAATCCATGGACCAGACTCACACTGAGCACGCAAAGCAGA[G/T]AGAATGAGTGAGTGCGCTCGCGCACACACACACACACACACCCACACTTGTACAGTTATCTTTGTATGGACATCATCAGACATTAATTTTATACTCTAGAGACTGTATGCAGGGTTTGAAATGAACCATTTTGCTTGGTAGCACCGGTGCTCCCAACTTTAAAAATGTAGGCGCACCAGTCAAAATTTAGTCACACTCACCAATTATAAGCACCGTTACTACAAGTTTTATACAAACATATTCATTGCATTTGAAATCAACAGTAATCAAACTAACAAGCAAAATATATATGCAAGCGTGAGGAAAATATGTCTCAACGAAATCCCGTTATCACAAGAAAATAGATTTTTATAACATAACTGAGTGACCAAAGCATACACGGAGCGCTCACCGGCCCTGCACACACTGCTTGACATGAATGAATCTGTTAACGATATAACTGTGCTGTTCTCACGGGTGCTGTCTGATATTGCACTGATGTGTTTGACATATACTGTACC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10176
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000047723 None None 288 None 6
ENSDART00000062336 Essential Splice Site 274 607 7 14
ENSDART00000129091 Essential Splice Site 621 954 12 20
ENSDART00000129693 Essential Splice Site 274 607 7 15

The following transcripts of ENSDARG00000042508 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 9 (position 3928048)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 3944427
GRCz11 9 3915956
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCCCTCCTAATCATCTTCATCCTCACCATGCCTCAGCCTTTACGCAAAGG[T/C]ACACACACACTMACTCAMAGAGAGAAAATATTCAAACTTTAATTTTACGA
Long Flanking Sequence:
TTGTCCTTGGATGGTAAAATGGGCTGCCTAAAAACAAAGTGGAAATTATACAATGAACAAAGCAACTATAAAAGAGAATTAAGATAGATGTAGGTGTACAAATCTTGATAAATTATATAGAGCAGTGTTTCTCAACCACATTCCTGAAGGACCACCAGCTCTGCTCATTTTTCACGTCTCAAACGAACACACCTGATTCAGAGCATCAGCTCATTAGCAGAGACTGAAAGACCTGTAATGAGTGCGACAAAGGAGACATCCAAAACATGCAATGCTGGTGGTCCTCCAGGTATCATGGTTGAGAAACACAGATATAGTTTATACAGATAAAACAGTTGTTTGGTGATTGATTTGTGTGTCTGCAGTGTTTCATTGTTTGTTTGTTTTTGTGTGCGCAGGTACTGTGATGAAGAGCGTCCTGAGGTTCCCATGCTTTTCCGAGACGTCCCATCCCTCCTAATCATCTTCATCCTCACCATGCCTCAGCCTTTACGCAAAGG[T/C]ACACACACACTCACTCACAGAGAGAAAATATTCAAACTTTAATTTTACGAACACTTTTTGTCATGCTTGGGGTGTTTAAATGTAATTAAGAGATTTTTGTATATTATGTCATAGTGAAAATGTATTTTCTTCTTGTTTTGAATCATTTAATTAAAGCTGCACAATTCTGGAAAAAAAAACGAGAATCGCGTAACGAGATTCATTAACAAATGAATCGCTCCCTCCGTTACAATTAGAAGTAAAAACAGGAGAGGTGCTTTATTTCAGGACATGGATTAGATCAAATTTTACAGGTAGGCAGGATGATACATTTCCATGCACACAAACACACGCTTTTTTTTTTAGACATGTCCCTGCGGTCACTTGTCTATCAATGTATAAAAGTGATGTAAGATTATAGTTTTAAATTTAATAAATAAAATTTAAATAAAAAAATATTTGCAAAACTCCAGATCATATAAATTTTGGTCCCACATTCATTTCAAAGTAGCGCTACCCTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa2488
Status:
F2 line generated
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
ENSDART00000047723 None None 288 None 6
ENSDART00000062336 Nonsense 422 607 11 14
ENSDART00000129091 Nonsense 769 954 16 20
ENSDART00000129693 Nonsense 422 607 11 15

The following transcripts of ENSDARG00000042508 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 9 (position 3918079)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 3934458
GRCz11 9 3905987
KASP Assay ID:
554-2681.1 (used for ordering genotyping assays)
KASP Sequence:
GGTTTAGCTGCTTCTGTTCAGKGCAGTGGATCCATGAGCAGCGCAGCGTG[T/A]CTGGAGTGGAACATCRGTGCTTTTGACTTGATCAGTCAGTGGTGCTCAGA
Long Flanking Sequence:
ACACTTTCAAACGACACCACTTACGGGGGTCTGGTGCAATGCTAGCCCTTTAAATCTGAAAGCGAAAGTCGATGACGTCACGGACCCGGTACCGGGTCCGCAGAGTTTAAGTGGTTAACCTGTTAAGCCTTTAAATGTCACTTTAAGCTGAGTACTAGTATCTATCAGGTCAAATAGTATGTTCTGTCATCATGGCAAAAATAAAATAAACCATTTATTGAAAATTAGTTATTAAAACTATTATGAAGGTATATAAGGTGAATGTATATACTACTGTTAATCCTATAGAAAATATTGAAATCTGGGCTGTACTTGCTGTATGTATATATAGATTTACAGCACGCTTTAAATGTATTGTTGAAATGAAGGTGATTCAATAATGGATGTTGTTTGCTTCTCTCTGCTTCATGACAGGTGGAGGAGGAGTTCTCTCTGCTGACGCGCTGTCTGGGTTTAGCTGCTTCTGTTCAGTGCAGTGGATCCATGAGCAGCGCAGCGTG[T/A]CTGGAGTGGAACATCAGTGCTTTTGACTTGATCAGTCAGTGGTGCTCAGAAGTCGTCGCTCTGTCCGACACGCCCTCCCAGCAGTCTGCGGTCAGTATCTGCTGCTCCTCCTAGAGCGAGAGCCCATAAATATAACGCATTAATGTTTAATATAATATAATATTGATGAAATATTTGAAAAAATATTCTTAAGATATTTGAAAAGGCTTTACAAAAAAAAGGACTTGATTTAACAATGTTAAGGCCTGTGCACACTGAGACGTTTTTGCCTTGTGTTTTACCTCGACGTTTAACGCCTCGTGACTAAACAAAGAGCGTCAATGTGATCGTGCCTTTAAAAAAAAAAAATGCTTCATGCACGGTTTTGTTTTGACGCGCCGTGTTAAATCTTCTCCATCAATCAGATCGGCACTTTTGTTCACGTGCACGGAGCTGCTGAAGTAACAGTAAACAGCACTTGGAGGCGCTCAAGCGCATAATTGTCAATGCGAGCGCACATT
Associated Phenotype:
Not determined