Busch Lab

ZMP

ubr5

Ensembl ID:
ENSDARG00000018192
ZFIN ID:
ZDB-GENE-030131-6559
Description:
E3 ubiquitin-protein ligase UBR5 [Source:RefSeq peptide;Acc:NP_001157866]
Human Orthologue:
UBR5
Human Description:
ubiquitin protein ligase E3 component n-recognin 5 [Source:HGNC Symbol;Acc:16806]
Mouse Orthologue:
Ubr5
Mouse Description:
ubiquitin protein ligase E3 component n-recognin 5 Gene [Source:MGI Symbol;Acc:MGI:1918040]

Alleles

There are 8 alleles of this gene:

Allele Name Consequence Status Availability
sa17638 Essential Splice Site Available for shipment Available now
sa22959 Essential Splice Site Available for shipment Available now
sa36265 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa22958 Nonsense Available for shipment Available now
sa22957 Nonsense Available for shipment Available now
sa36264 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa17638
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:
A > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000035761 Essential Splice Site 1533 2795 36 59
ENSDART00000111869 None None 139 None 5
ENSDART00000128437 Essential Splice Site 1554 2816 35 58
ENSDART00000134444 Essential Splice Site 1560 2822 35 58
ENSDART00000141985 None None 248 None 5

The following transcripts of ENSDARG00000018192 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 16 (position 56191242)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 52699742
GRCz11 16 52585485
KASP Assay ID:
2261-0376.1 (used for ordering genotyping assays)
KASP Sequence:
CACRAAATGATTTRGTGTGCATCTGAATCTGAGTKGAAATGTTTTCTTTT[A/C]GCTCCAGTCAGTCTGCCTCTTCATACATCATCAGGAACCCGCAGCCCCGC
Long Flanking Sequence:
CTTATTTTCTTTAGCAACTTCATCCCTCAGCCTATTGGGAAGTGCAGGCGTGTGTTCCAGGCACTGTTGCCGTACGCAGTGGAGGAGCTCTGCAATGTGGCCGAGTCTCTGATCGTGCCGGTGCGTATGGGCATCGCTCGGCCCACAGCTCCCTTCACTCTGGCCAGTACCAGCATTGATGCAGTGCAGGGCAGTGAGGAGCTCTTCTCTGTGGAGCCTCTGCCACCTCGACCCTCCCCGGACCAGTCCAGCAGGTGAGATACGCTTTAGTCAAACCCAAAACACATAACACCACGATTCATTTGAAGCTTCCTGCTTTCCAGACAGTGCAGAAATCGATGTATAGCCATTCATGAATTATTTCTTAGACTTTCAAAAGGCATTTCTATTCTCTCTGCTATGAATCTCTAAATGGATGCCTTTGAAATTCTGATAGTATGAAAAGGATATCACGAAATGATTTGGTGTGCATCTGAATCTGAGTTGAAATGTTTTCTTTT[A/C]GCTCCAGTCAGTCTGCCTCTTCATACATCATCAGGAACCCGCAGCCCCGCCGCAGCAGCCAGTCTCAGACAGCCCGCGGACGGGACGAGGAGCAGGATGATATCGTGTCTGCTGACGTAGAAGAGGTATTAACAACTATTTCAACACTTTAAAGAACCATTCATGATATTAGACTCTGTCCTTTTAATCTGCACATTTAGTCCTGCTTAGGATAGATTACATCAGTGTGACAGTAGTAGGGTTGTAATGATATTAATAATAATATATTAATAATATTATACTATTCAAAGTGGTTGATGTCATGCATATTGATATCCTGTAAGAGTATGAATTTCTGAACGGAACTGACTGTCTTTAAAAAGCCTTTGTACGATACATATATTAAAATAGTGTTTCTGCTTCTTATTTTATGTAATAGGACTCTAGTTTCACCGAGTTAGGTCAGGCCATACGTTTTTTGCTTCAACTTATGAAAGCAGCATGTATGAGGCTTATTAGCG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa22959
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
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000035761 Essential Splice Site 1574 2795 36 59
ENSDART00000111869 None None 139 None 5
ENSDART00000128437 Essential Splice Site 1595 2816 35 58
ENSDART00000134444 Essential Splice Site 1601 2822 35 58
ENSDART00000141985 None None 248 None 5

The following transcripts of ENSDARG00000018192 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 16 (position 56191115)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 52699615
GRCz11 16 52585358
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGGACGGGACGAGGAGCAGGATGATATCGTGTCTGCTGACGTAGAAGAGG[T/C]ATTAACAACTATTTCAACACTTTAAAGAACCATTCATGATATTAGACTCT
Long Flanking Sequence:
TGGGCATCGCTCGGCCCACAGCTCCCTTCACTCTGGCCAGTACCAGCATTGATGCAGTGCAGGGCAGTGAGGAGCTCTTCTCTGTGGAGCCTCTGCCACCTCGACCCTCCCCGGACCAGTCCAGCAGGTGAGATACGCTTTAGTCAAACCCAAAACACATAACACCACGATTCATTTGAAGCTTCCTGCTTTCCAGACAGTGCAGAAATCGATGTATAGCCATTCATGAATTATTTCTTAGACTTTCAAAAGGCATTTCTATTCTCTCTGCTATGAATCTCTAAATGGATGCCTTTGAAATTCTGATAGTATGAAAAGGATATCACGAAATGATTTGGTGTGCATCTGAATCTGAGTTGAAATGTTTTCTTTTAGCTCCAGTCAGTCTGCCTCTTCATACATCATCAGGAACCCGCAGCCCCGCCGCAGCAGCCAGTCTCAGACAGCCCGCGGACGGGACGAGGAGCAGGATGATATCGTGTCTGCTGACGTAGAAGAGG[T/C]ATTAACAACTATTTCAACACTTTAAAGAACCATTCATGATATTAGACTCTGTCCTTTTAATCTGCACATTTAGTCCTGCTTAGGATAGATTACATCAGTGTGACAGTAGTAGGGTTGTAATGATATTAATAATAATATATTAATAATATTATACTATTCAAAGTGGTTGATGTCATGCATATTGATATCCTGTAAGAGTATGAATTTCTGAACGGAACTGACTGTCTTTAAAAAGCCTTTGTACGATACATATATTAAAATAGTGTTTCTGCTTCTTATTTTATGTAATAGGACTCTAGTTTCACCGAGTTAGGTCAGGCCATACGTTTTTTGCTTCAACTTATGAAAGCAGCATGTATGAGGCTTATTAGCGTTTCCTTATATTTTAAATGGAAAAAGCACAAGCAAAGCCATGACATGTTTATATGAAGACATGTCTTTTATTTGCCTGATTTGACTTTAAGGTCTGTTTTAATATTTCAATTTCACATAGAAAAATG
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa28751
Status:
Less stringent filtering
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000035761 Nonsense 1604 2795 37 59
ENSDART00000111869 None None 139 None 5
ENSDART00000128437 Nonsense 1625 2816 36 58
ENSDART00000134444 Nonsense 1631 2822 36 58
ENSDART00000141985 None None 248 None 5

The following transcripts of ENSDARG00000018192 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 16 (position 56189247)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 52697747
GRCz11 16 52583490
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCATGATGACCAGGAGGAGCAGGGAGAGGAGAACGCAGAGGCTGAAGGA[C/T]AGCATGATGAGCACGATGAGGATGGTAAAACACACCATCGATTATTAATA
Long Flanking Sequence:
TTGAATCGATGGCATGATAATCGCAACTGAACCCTGAGACCAGTGTAGGTTCACACCTATTAACAACTGTTTATTAACAACTGTTTATTAAGTGCAAGGTTTGATACTGATTAGAACTTGAAGTGGTGATGATGTCTTAAAATATCCTGAGAATGTCTTAAAGTATTGAAATTACTTTTAGGATTCCTACCCTAAATAAAAGGGCAGCTTTTCATTTATTGTAAATGATGTAAATATGTATATAGTTCTTGTACATTGTACATAATATTTTGTAAAAAAAAAAAAAAAAAAACTGAAAATCAAGTGTAATTAAAATCAAAATTGTACATCAAATCCAATTGTGAGTTGATCAAAGAGTTCCATCCCTGGTCAGTATTGATTTGAATTGCTACCTGGACTGTTTACCTGTACAGGTGGAGGTGGTGGAGGGTGTTGCAGGTGAGGAGGATCACCATGATGACCAGGAGGAGCAGGGAGAGGAGAACGCAGAGGCTGAAGGA[C/T]AGCATGATGAGCACGATGAGGATGGTAAAACACACCATCGATTATTAATAAAGAGGTTGACAATATCTCTTTCATTTAATGGACCAACATTATTGTCATTCATTCATATTCCTTCGGTTTAGTCTTTTTATTCATCAGGGGTTGCCACAGAGGAAAGAACCGCCATCTTATCTAGCATATGTTTTACACAGATGCCCTTCAGCCACAACGCATCACTGGGAAACATCCATACACACTCATACACTACGACCAATGTAGTTTATTCAATTCCCCTATAGCGCATGTGTTTGGACTGTGAGGGAAACCGGAGCACCCGGAGGAAACCCACGCCAACACGAGGAGAACATACAACTCCACACAGAAACGCCAACTGACCCAGCCGGGACTCGAACCAGCGACCTTCTTACTGTGAGGCGACAGTGCTAACCACTGAGCCACCGTGTCACCCCACCAACATTATTTCATAATAATCGTAATGTTTAGGGAATATCAAACAGCAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa36265
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000035761 Essential Splice Site 1656 2795 39 59
ENSDART00000111869 None None 139 None 5
ENSDART00000128437 Essential Splice Site 1677 2816 38 58
ENSDART00000134444 Essential Splice Site 1683 2822 38 58
ENSDART00000141985 None None 248 None 5

The following transcripts of ENSDARG00000018192 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 16 (position 56184366)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 52692866
GRCz11 16 52578609
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGGGCTAATAGTTCTGACTTCAACTGTATATTTTCTACCTCTTTTCTGAA[G/T]GTGCCAGCAGTGTTCCTGCTTTCTTCTCCGAGGACGACTCCCAGTCGAAT
Long Flanking Sequence:
CCACACTTTGGCTTAAAAAAGGTGCAAGAACCCTGTGTACAGATAAGTGTCCTAAAATAAAGCATGCATGTACATTTTTTTTTCTTGAGAGGCTTTTTTATTTTGGCTAGAATAAAAGCAGTTAAAAAAAAAAGTTTTTAATTTTTTTTAAAGCTATTTTAAGGTCAATATTATTAGCCCCCTTAAGCAATATTTGTTTTGAATTGTCTACAGAACAAACCACTGTTATACAATGACTTGCCTAATTACCCTAACTTTAACCTAATTAACCTAGTGAAGCCTTTAAATGTCACTTTAAGCTGAATACTAGTGTCTTGAAGAATATCTAGTCTAATATTATGTGCTGTCATCATGGCAAAGAGAAAAGAAATCAGTTATTAAAACTATGTTTAGAAATGTTAAGAAAAATATTCCCTACCTTAAACAGAAATTGGGGGAAAACAATAAAGGGGGGCTAATAGTTCTGACTTCAACTGTATATTTTCTACCTCTTTTCTGAA[G/T]GTGCCAGCAGTGTTCCTGCTTTCTTCTCCGAGGACGACTCCCAGTCGAATGACTCCAGCGACTCGGACAGCAGCAGCAGCCAGAGTGACGATGTGGATCAGGAGACGTTTCTGCTGGACGAGCCTCTTGAGAGAACCACCGGCTCAGCACATGCTAACAGTGCAGCCCAGGCCCCACGCTCCATGCAGTGGGCTGTTCGCACTACACCCAGCCAGCGCTCTGGAGGTGGCGCCCCATCCAGCTCGTCCGCTCCTGCTGGTCAGTGTCCAGAATAACACAAGTTGCAAAAGTCACAACAGCAAGTCCCAGAAGGGGTCCGTTCTTCATAGGTGGATTACTCAGTTAGCTGGATTTGGTTATTGACGATTTGACATGATCCAGGATTGTTTCGTTTTTCAAAACTGATCCGAGAGTTGTTGTCATAGCAACAGTTCTGGTAGCTCAAACCTGGTCGGAAGCAGGTTCAATTCATATAAACAGGATTAGATCGGGTCAGTTTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa22958
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
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000035761 Nonsense 1683 2795 39 59
ENSDART00000111869 None None 139 None 5
ENSDART00000128437 Nonsense 1704 2816 38 58
ENSDART00000134444 Nonsense 1710 2822 38 58
ENSDART00000141985 None None 248 None 5

The following transcripts of ENSDARG00000018192 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 16 (position 56184285)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 52692785
GRCz11 16 52578528
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGACGACTCCCAGTCGAATGACTCCAGCGACTCGGACAGCAGCAGCAGC[C/T]AGAGTGACGATGTGGATCAGGAGACGTTTCTGCTGGACGAGCCTCTTGAG
Long Flanking Sequence:
TTCTTGAGAGGCTTTTTTATTTTGGCTAGAATAAAAGCAGTTAAAAAAAAAAGTTTTTAATTTTTTTTAAAGCTATTTTAAGGTCAATATTATTAGCCCCCTTAAGCAATATTTGTTTTGAATTGTCTACAGAACAAACCACTGTTATACAATGACTTGCCTAATTACCCTAACTTTAACCTAATTAACCTAGTGAAGCCTTTAAATGTCACTTTAAGCTGAATACTAGTGTCTTGAAGAATATCTAGTCTAATATTATGTGCTGTCATCATGGCAAAGAGAAAAGAAATCAGTTATTAAAACTATGTTTAGAAATGTTAAGAAAAATATTCCCTACCTTAAACAGAAATTGGGGGAAAACAATAAAGGGGGGCTAATAGTTCTGACTTCAACTGTATATTTTCTACCTCTTTTCTGAAGGTGCCAGCAGTGTTCCTGCTTTCTTCTCCGAGGACGACTCCCAGTCGAATGACTCCAGCGACTCGGACAGCAGCAGCAGC[C/T]AGAGTGACGATGTGGATCAGGAGACGTTTCTGCTGGACGAGCCTCTTGAGAGAACCACCGGCTCAGCACATGCTAACAGTGCAGCCCAGGCCCCACGCTCCATGCAGTGGGCTGTTCGCACTACACCCAGCCAGCGCTCTGGAGGTGGCGCCCCATCCAGCTCGTCCGCTCCTGCTGGTCAGTGTCCAGAATAACACAAGTTGCAAAAGTCACAACAGCAAGTCCCAGAAGGGGTCCGTTCTTCATAGGTGGATTACTCAGTTAGCTGGATTTGGTTATTGACGATTTGACATGATCCAGGATTGTTTCGTTTTTCAAAACTGATCCGAGAGTTGTTGTCATAGCAACAGTTCTGGTAGCTCAAACCTGGTCGGAAGCAGGTTCAATTCATATAAACAGGATTAGATCGGGTCAGTTTAAGCAAAGATAATGCAGAAAGTATGTGCCGAATTCTGATATTTTCTTACAGTAGTAGTTATATACACTTGGGAAAATATTAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa22957
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000035761 Nonsense 2079 2795 45 59
ENSDART00000111869 None None 139 None 5
ENSDART00000128437 Nonsense 2100 2816 44 58
ENSDART00000134444 Nonsense 2106 2822 44 58
ENSDART00000141985 None None 248 None 5

The following transcripts of ENSDARG00000018192 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 16 (position 56173856)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 52682356
GRCz11 16 52568099
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCAATGCCAGAAAGGAGGATTTGTTTGGACGGCCTAGTCAAGGTCTATA[T/A]TCGTCCTCATATATGGCCAGTAAAGGCCTCACCGATCTGACTGTGGACAT
Long Flanking Sequence:
ATCTACAATGATGAGGAGCATGGTTACTTACTGAGTTATTAATGCACAGCAATACCACATGAGGAAAGGACGGACTTTGAAGGAATGAACAGTGTGAGGAGAGCTCCATTATAGTGCACTGGACATGTCTGAACGTGTTCCGCCCACGTGTGCGCAAGGCAGGCAGTTCTGTACAATTACGTAATTTATCGGCTTAAAGATAGCGGCCTAATTTAGACATCGGAGAACGTTAATCTTAAAAATAGCATTTATCGGACGATAACGATATGGCCACCGATATATCGTGCATCCCTAAAATATATATATATTGAATTATGAAGTTGCTATTTTGCAGCATGTTTTTATCTATATTGATCATGCCTTTTAATAGCTATATGTAACACATTAGAGGTGTTTTTGGGATCAGTCCAGATGGTTGAGTTTAACACTGCTGTTCTTCCTCTTCATCAGCCCAATGCCAGAAAGGAGGATTTGTTTGGACGGCCTAGTCAAGGTCTATA[T/A]TCGTCCTCATATATGGCCAGTAAAGGCCTCACCGATCTGACTGTGGACATGAATTGCTTGCAGGTAAACATGATCGTCGTACTAGTGCTGTAGTAGATGGTGCCATTTCTAGGTTAATTTGCCTTAAAGTCCCTCATTCATCATCTCTTTCAGTCATTCATTTAATAGATTTTTTTGTACTTTATTTAAATTTTAAATAAATATTTTTTTGTTTGTTAATTCAATTAATTTTATATATTTAAATGTTTAAAATATTGCATAAACAGAAGTGCATCAGTAATATAATAAACTTTGTATGCTTTTCTGAACAGCTCTTAACAAAGAATTTTATACCCACAAATGTTGCCTTTCAGTCTGTTGCATTCTATTATTTATTTTCATTTTCATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAAAACTAAATAAATATGTAACTAAATAAATATAAACACATAAATATATAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa36264
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000035761 Nonsense 2503 2795 53 59
ENSDART00000111869 None None 139 None 5
ENSDART00000128437 Nonsense 2524 2816 52 58
ENSDART00000134444 Nonsense 2530 2822 52 58
ENSDART00000141985 None None 248 None 5

The following transcripts of ENSDARG00000018192 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 16 (position 56159696)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 52668196
GRCz11 16 52553939
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGAGCTGGATGACCCTGATGATGGGGATGATAACGCTCCTCTGTTTTAC[C/T]AGCCTGGAAAGAGGGGTTTCTACTCACCACGTCCCGGCAAGAACACTGAG
Long Flanking Sequence:
CAATGTTTAAGAACGTGCTTAACAGTGCTCAAATGTTAGCGGGAAATGGATGTTTTTAAAACTTAAGTATCGATTGGTACCAAATTCTAATATCGTGACAACCCTATATATATATATATATATATATATATATATATATATATATATATGATTTATAGATAGAAAGATTTTTAAAAAATAAGTGATCATGATCTTGTCCTCTTTTTCACAGGGAAAATGGTGCTGACAGTATACTAGACCTCGGCCTCCTCGACACTCCTGAGAAAGCACAAGTATGTTCTGTCTAAAATCATAAAAGTTGGATTTTCTAGTGTTTTCCAGTTGATCTTTATTGTTTTCCATATTAAAGTTTTAAAGCTGTAACATGAGATCTGAATGGAACTGTATTTCCTACATTTCTCCAGCAGGAGAACCGAAAGAGGCATGGTTCGACTCGCAGTGTGGTGGACATGGAGCTGGATGACCCTGATGATGGGGATGATAACGCTCCTCTGTTTTAC[C/T]AGCCTGGAAAGAGGGGTTTCTACTCACCACGTCCCGGCAAGAACACTGAGGCCAGGCTCAACTGTTTCCGTAACATCGGCAGGTAAGAGACATGTGTTTTTGCACTTTTATGCATAAAGCAAAGGTTAAAAAAATCAGCCCCGGGCAAACATTCATTGCAAAATAAGTTTGTTTTGTGTAATATATGTGTGTGTACTTTGTATGTCTGTCTTTATCTATCTATTTGTCTATCTATCTGTCTGTCTGTCACTGTCTCTCTCTGTCTGTCTGTCTGTCTGTATCTATCTATCTATTTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCACCTTTCTATCTCTGTCTGTCTGTCTGTCTATCTATCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCT
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa4685
Status:
Allele not cryopreserved
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000035761 Nonsense 2715 2795 58 59
ENSDART00000111869 None None 139 None 5
ENSDART00000128437 Nonsense 2736 2816 57 58
ENSDART00000134444 Nonsense 2742 2822 57 58
ENSDART00000141985 None None 248 None 5

The following transcripts of ENSDARG00000018192 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 16 (position 56150391)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 52658891
GRCz11 16 52544634
KASP Assay ID:
2261-0371.1 (used for ordering genotyping assays)
KASP Sequence:
AGAATGCAGAGAAGCTGCTGCAGTTCAAGCGCTGGTTTTGGTCCATCGTT[G/T]AGAAGATGAGCATGACGGAAAGGCAGGACCTGGTGAGACACTACTGCATG
Long Flanking Sequence:
ACATCTACCTATTTTCCAAGTGAGTTTTGGGACATTTCAAATAAATGTAAATGTGACAAGGGTGCTAAAGAAAAAACTAAAACTCCAGTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTAAATCATCCACAAAACCAGTGTTTAAAACATGAACGTATTGTATTCCTGATTAAAATAAAATTGTACCTGCTTTGTACTCAAATTTATTTGTAGATTTTTATTTTTATTTTTCTAAATTATAAGAAAAATATTACATTTAATAAATTTGAGTATAATCTTATTGCTTTAAGGTTGCTATATATATATATATATATATATATATATAATGGTATAAAGGTTTTTTTTTCTTCTATTTGTTTTTTAATAATGTAATTTACTTATAAGCTAAAGTCATCCATTGTGTGTTTTGTGCTTAATTGTGAGTTGTGTTTTACCCTGCAGGTGAGAATGCAGAGAAGCTGCTGCAGTTCAAGCGCTGGTTTTGGTCCATCGTT[G/T]AGAAGATGAGCATGACGGAAAGGCAGGACCTGGTGAGACACTACTGCATGCCTTTACTCCACATTAGACACGTCCCAGCAGTTGGATTTGTCCATATTTAACCGAGCAGTTGGATTTGTCCATAATAAAATAATATATTATAATTGAATGTAAATGGCACAATTTAAACCAATAGCTGGTTTATCCATAATTGACCCAGCATTGGTTATTTTTTAAATTAAATTAAATTTACACTTTTTTTATCCAATGGTTGGGGTTGTTAATATTTAACACAGCATTGTTATTATTATTATTACATTTAAATGACACTTTTTTAACCCAATGGTTGGGTTTGTTCATGTGTAACCCATCATTGGGTGAATTATTTTTTAGTCTTGTTTTTTCATAAAATTTTAAATAAGTTTTAACCCAACTTATGGGTTTTTTCCTATTTAACCCAATTTTTGGTTACCCAATAATAAGCTTTTTCTCTGTTTAACCGAACTATGGGTAATTATTAT
Associated Phenotype:
Not determined