ZMP
PBRM1 (1 of 2)
Ensembl ID:
Description:
polybromo 1 [Source:HGNC Symbol;Acc:30064]
Human Orthologue:
PBRM1
Human Description:
polybromo 1 [Source:HGNC Symbol;Acc:30064]
Mouse Orthologue:
Pbrm1
Mouse Description:
polybromo 1 Gene [Source:MGI Symbol;Acc:MGI:1923998]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa27716 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa35009 | Nonsense | Available for shipment | Available now |
sa41765 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa17189 | Essential Splice Site | Available for shipment | Available now |
sa31812 | Essential Splice Site | Available for shipment | Available now |
sa970 | Nonsense | Available for shipment | Available now |
sa31811 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa27716
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000045971 | Nonsense | 107 | 1559 | 3 | 28 |
Genomic Location (Zv9):
Chromosome 11 (position 4013602)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 3932106 |
GRCz11 | 11 | 3951493 |
KASP Assay ID:
2260-3860.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGCCCATTGATATGATGAAGATCCAGCAGAAGCTGAAGATGGAGGAGTA[T/G]GACGATGTTGAGCAGCTCACAAGCGACTTTCAGCTCTTATTCAGTAATGC
Long Flanking Sequence:
TGGTTCAAAATGTGAAAATAAACCTGCACTCCTATGAAAATATCAAGAAATCAGGCCCTACACACCTTGCACCTTATTGCCCACTGTGTTTATTTAAATTTAGCCTATATCAATTGTTTGCAACCACTTACCCTAAAGAAATGTAGTAAATCCAATTAATCACTTTCTTTTTAGTGTATGCAGATTAGCCCATAATCTTCTATTTACAAGACTCCTAATTTTGTTGTGAATGTTATACAATAGGTTCAAATCTACCAAGGACAAAAACAAAAAACAATATTCTTATAATATACACAGCATTACTCTTTAGCAGTCACTCCAGGCTGTTTCGGAAAACATACATAGCACATTTATATGTTTAAATGTGAAATATTAAAGGATTCAAATTTATTACAAATTTACTAATTTTCTCCCCACAGGAATCAGCCAGATTACTATGACGTGGTGTCACAGCCCATTGATATGATGAAGATCCAGCAGAAGCTGAAGATGGAGGAGTA[T/G]GACGATGTTGAGCAGCTCACAAGCGACTTTCAGCTCTTATTCAGTAATGCCAAGACATACTACAAAGTAAATATCACTATCTTACACTACCATTCAAAGGTTTGGAGTTAGTACAAGTCTCTTTATGCTCGCCAAGGCTAATTCGGTAACACTTTTACTGTTTTTTTTTTTTGCTTTGTTTGTCAAAGTTGCAGTCAAAGGTAGAAAAGGTTGGGACAGTATGGAAAACGCAAATAAAAAAAAGAAAGTAGTGATTTCTAAATTAACTTTGACTTGTATTTCATTACAGACAATACAACAAACATTATTTAATGTGCTCCTCATGATAACAAACACATATTCCAATTTTGATTCTTGCAACACATTTAAACAAGTTGGAGTAGTGAAGCATTTATCACTTTGTAACGTTGCCATTCCTTTTCACAACACTTAAAGCATTTAGGGATTGAAGACAGAAAGTGCAGAAGTGTTTCAGGTGTAATTTTTTTCCACTCTTTCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35009
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000045971 | Nonsense | 154 | 1559 | 4 | 28 |
Genomic Location (Zv9):
Chromosome 11 (position 4008638)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 3927142 |
GRCz11 | 11 | 3946529 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGCTTGTAAACTGTGGGATCTGTATATTCGGACCAAAAACGAGTTTGTG[C/T]AGCGAGGAGACTATGATGAAGATGATGATGATGACGACCCACAGGAGAAC
Long Flanking Sequence:
GATAAGTTGGCGGTTCATTGCTCTGTGGCAACCCCGGATTAATAAAGGGACTAAGCCGACAAGAAAATGAATGAATGAATTATTTTGTGATACTAAAGACACCAGCGCTATCACAGGTCTTTTTAAAGAAAAAAAATATCACCACCTCACTTTCATACCTGTATTTTTGATCAAATCAATAGATAAATCAAAATAAATTTCATTTGGTGAGCAAAAGGGATGAAAAACATAGTTAGCTTGTAAACTACATGTATGTTTTGTTTTAATTATTGTACCACTTAATTATCTAATATTGTACTATGAGGATATGAGATTGAAATATTGTTGTTTATAGTATGATTTGTGATGTTCCTTTTTTAGATATCTACAAAATAAATAAATATCAGTTAAAATAAAACCTGAAACCTCTTTTTTGTGTTGTTGTGCAGCCTGAAACTCCAGAATACAGAGCAGCTTGTAAACTGTGGGATCTGTATATTCGGACCAAAAACGAGTTTGTG[C/T]AGCGAGGAGACTATGATGAAGATGATGATGATGACGACCCACAGGAGAACCTCGGAGGAGCCACAGAGGAGGAGGTCAGACCACATACACATCTACTTAGTCAAACACTGCACATCAAATTTATGGGTTAGACTTCTGGTGTGAGGAAAATAATGACACCTCATTGTACACGGTTTTTAAAACAAAGAAAAATGAGGACACAAATGTGATTAATATGTGGCTTTGCGTTTACAGTCTATGTCGAGCCTTAAGGAAGTTCTTGGGATGCTTCTGGATGCTGTGTTGACCTACACTGAACACGGCCGCCTTATTAGCGAACTTTTCCAGAGACTTCCCTCTAAAATGGTAGCTTTTCAGTTTCATATATGGACATACACAAACATATTAATATTATATCTTTAGTTTAACTCTGTTTTTATTGAAATATGTTAGTCAGAGAGCCACAGCATCAGATACACAGAATCATTAGACATCAACTGATCCAATGTGGTGGTAGAGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41765
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000045971 | Essential Splice Site | 238 | 1559 | 6 | 28 |
Genomic Location (Zv9):
Chromosome 11 (position 4007067)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 3925571 |
GRCz11 | 11 | 3944958 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATTATTAAAGAACCAATCGATCTGAAGAGCATCGCACACCGAATACAGG[T/A]ATTATGATCACATTATTTTACATAATTATATAGAGTATCACTGATCTACA
Long Flanking Sequence:
GCATGGCTCAATATCTAAAAGAAAGCATTCAGAAATTGATTTAAAAATTGATGCCCAAAAAGTGCTTAGCGCTGGACAAAGCCAGAAAGTATGAAGAAGAGTGGCTGGAGCTTGTCGACACCGATCACAAGTTGGATCAAAACCAGGGTTAATTTTAGATATTTTTGCCTTAGTCCAATATACTCTATGCAATAATTTGAATTGTATAAGGGAATGACGAGCACAAATAGAAGAGGTTTGTACACGAGACAGAGCCTTGAACCATTCCTCGTCTGTGAAAACATGATTGAGATCTGATTCCCAGCTCTGCTTTATTTTTAAAAAGGATGAGGAATCTAACTGTCTAATAAATGAAAAAATTGTTTTATAAATTTTAGAGACTGCACCTTTATTAATATTATATCTTAATAAATATTCACTCTTTTTCCAGCAATATCCAGATTATTATGCTATTATTAAAGAACCAATCGATCTGAAGAGCATCGCACACCGAATACAGG[T/A]ATTATGATCACATTATTTTACATAATTATATAGAGTATCACTGATCTACACTAAATTTATGTTTTGCTTTCCCTAGATGTGCTACTATAAAAGTGTAAACCATATGGCTAAAGACATTGACTTGTTAGTCAAAAATGCCAAAACCTACAATGAACCCGGATCACAAGTGTTTAAAGTAATGTATCACTGACATTTCTATATACGATTTATATAATGATTAGACTTTCACAGTTAAGCTTAGTTGTAATTTATATAATGCAAAATGTGGTCTGCTTATAAGTATAATTTAATCATGAATTTCCAGGATGCGAACACAATCAAGAAGGTCTTTGCGCAGAAAAAACTGGAGCTCGAACATTCTGAACCTATTAAATGCAGCATCAGGATCAGGTAAGTGTTATGAAGCATGTTTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17189
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 |
---|---|---|---|---|---|
ENSDART00000045971 | Essential Splice Site | 403 | 1559 | 11 | 28 |
Genomic Location (Zv9):
Chromosome 11 (position 4001489)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 3919993 |
GRCz11 | 11 | 3939380 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGAATAAGCCTGGGTTGACTGTATGATGACTGACTTGTTTTTTTCWCCA[G/A]GAGTAAGATGAAGAATAATGAGTATGAAAGTGTGGAGCAGATCGACACAG
Long Flanking Sequence:
AGGGAAGTGGGTGTTCGGGTCAATCGGTGCTTTGGAAAACACTATCAGTTGGGTTTAGGGAAGTGGGTGGGCGGGTCAATCTGGGCTTTTGAAAACACTATCGGTTGGGTTTAGGGTAGTGGGTGGGCGAGTTAATCTGTGCTTTTGAAAACACCATCGATTGGGTTTAGGAAAGTGGGTGGACGGGTCAATCGGTGCTTTTGAAAACACTATCGGTTGGGTTTAGGGAAGGAGAAGGGTGGGCCAGTCAATCTGTTAGTCAGTCATTTAGCAACCTCTGGTGAATTTACGCAAGAACAGCAGGTGATTGGTACGCGCGAGAGAAATTTGAAATCTCAAAAAGGGTACACATCAGCCTCTGGTGGATTCATGAAAACAAAAACTGCAAAAAAAAACGTAGCTCCTGGGACGTATTTGGTGCTCTCCAGAAATGTGTATAGTGGTACGTTTCAGAATAAGCCTGGGTTGACTGTATGATGACTGACTTGTTTTTTTCTCCA[G/A]GAGTAAGATGAAGAATAATGAGTATGAAAGTGTGGAGCAGATCGACACAGACCTGAACCGGATGTTTGAGAACGCCAAGCGCTACAACGTTCCCAGTTCTCAAATCTACAAACGTGTGCTGAAGCTGCAGCACATATTGCAGGTAAAATAAATACCTGCTTATAAAGGATTGTGAACGTGGTATCTCTTCACTGAACAGTAAATGATGATTACATACAAGTCATAATTATTAGCCCCCCTGTATATTTTTACCCTAATTTCTGTTTAATGGAAAGAAGAATTGTTTTCAACACATTTCTAAGCATAATAGTTTTAATAACTCATTACTAATAACCGATTTCTTTTATCTTTGCCTTGATGACAGCACAAAATATTTGACTAGATATTTAGTATTCAGCTTAAAGTGACATTTAAAGGCTGAAAATTCAATCAATGCTTGACATTGTATCAAGCCATCGTGTCTTTTCTTTGTTTGTGTGTATGTGTGTTCAGATGAAGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31812
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 |
---|---|---|---|---|---|
ENSDART00000045971 | Essential Splice Site | 895 | 1559 | 17 | 28 |
Genomic Location (Zv9):
Chromosome 11 (position 3991269)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 3909773 |
GRCz11 | 11 | 3929160 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAATGTGTTGTGGTGCAGATGCCTGTTGATTATCAATGATTTGACCTGCA[G/A]AGGCAGAAAAGAGCGAGGACACGGCGGGCGGAGGATGGCAGGGAGCCCTG
Long Flanking Sequence:
TCACTTCATGACCCCTTTAAAGTCTAAAGGAGTATAACGGCGTTTAAAGCAGTTTTTGTTTTTAAGTGGTCATTAAATGAATAGCTAACCTAAAACAAAAAATGTTGTCATCATTTACTTGTCGTGAACATGTTTGAGTTTTATGTAACACAAAAGAAGATGTTATGAAAAATGTTGGAAAGCTGTAACCATTGACTTCCATTGTATTTGTTTCTCCTACTATGGAAGTTATTGATTTGAGGTTCCTATCATTTTTCATAATATCTTCTCTTGTGTCCAACAATCTCGTAGAAATTTGAAATCACTTGAGGGTGAGTAAATATGGAGTAAATTAGAATTTTTAGGTGAACCGTCACTTTAATACTAGTGCAATATGCAATTACATTATAGGTTACACCCTTTGATAGTCTGTAACTTTGATTAAATTTAAACTCTGAAATAAAGTTGTTATAATGTGTTGTGGTGCAGATGCCTGTTGATTATCAATGATTTGACCTGCA[G/A]AGGCAGAAAAGAGCGAGGACACGGCGGGCGGAGGATGGCAGGGAGCCCTGCAGCGCAACTACAGCCAGGACTGCAGCTTTAAGGACAACATGTACCATGTGGGTGACTATGTGTATGTGGAGCCCACCGAACCGAACCTGCAGCCACACATCGTCTGCATAGAGCGCCTCTGGCAGGACGATGCAGGTACTACATTTACAGAAAGTGCAGTTGCTAATTTATTCTGTTTAAAGTTTACATGAAGTGAAAGCTGAGACTGTTTGTTTTCGTATTGTCATGCAGTTCCTAGAGAAAGAGAATATTAAATGGGAAAACAGTGGGCGTGGCTTGTTTTTTCAACTGCGAGCTGATTGGATGGGGTAAAGTAGGCATTTCATTCAGGAAGATGTGTGAAATGGTTTGGGGAGGGTTAATACAACCTAACAGACTCCTCCTGCTCACAATTACTGTCAAAACTGATATCTGGAGGGGCGTGGTTGAGTATGTTAGCCACACCCAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa970
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000045971 | Nonsense | 1232 | 1559 | 22 | 28 |
Genomic Location (Zv9):
Chromosome 11 (position 3985128)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 3903632 |
GRCz11 | 11 | 3923019 |
KASP Assay ID:
554-0875.1 (used for ordering genotyping assays)
KASP Sequence:
CGGAGGAGGACGTGTTGCTGTGTGAGAGCCGCTACATCGAGAGCGAGAAG[C/T]AAATGAAGAAGTTTAAAGGGCTGAAGCGTTTCTCTYTGTCCGCCAAAGTA
Long Flanking Sequence:
AAATAAACAAGTATGTTTACGTACCATTTTTCTCAACTACCTGCAGACTTATTATGGTATTTTTATGTTTTAGAGCAGTCAAAAACATACATACAGCACCTTTAAAAGCGCATAGTGTGAATTAATTCAGGGCACAAATGTTTCAGTACACTGGAAGATTCTCGAGATGGCTGATGCCCTGTTCAATGCACTGACTACTAAACAAATAGATGATTGACCTTTCAAATGTACGCACATTTCCATCAAGATAATACACATTAAAATATGTAAATGAAAACCTAGCTACTGACTGAAGGAAATTGACTCTAAACTCGGTTATTGACAATGAAAGAACTACTATTACATGAAGTGATTTGTTCAGATCTTTTGTGGACTGCTCTTCCTTTTCCTCAGGGAAGTGTACAGTGTCTTCTTTCAAAGATTTCCTGTCATGCCGGCCGACTGAGATGCCGGAGGAGGACGTGTTGCTGTGTGAGAGCCGCTACATCGAGAGCGAGAAG[C/T]AAATGAAGAAGTTTAAAGGGCTGAAGCGTTTCTCTCTGTCCGCCAAAGTAGTGGAAGATGAAATCTATTACTTCAGGTCTGTCAACCTGGTCTATCTACTACTAAACGACTCATCTAAAGAAAAAAAAAATTGTATACAGCGGGGAAAATAAGTATTGATAAGTGTTGACACAGCCATGTGACAGCTGCTGCGCTCGTGCATCCAGGTTAATCATGAACAACTCAGTGCGCATGCGTTAGTTGCACTATTGCGGTCTGATTATGTTTCAATCAAGGTTTATATGCATCAAATGCATAACATCTGTGCCAAACATTTCAACTGACGAACATATTAACAATAATACAACCGTATAGCCGAATTAAATGTATGCATTGGCATGTTACAGCCCTAATGAGTATGATTATGTGAAACTCCATGTAGATAGATATTGCAATGATTTCGGGTACTTACTTAGCGATGCACGCACACATAACGTTAGATGCACAATCCTTAAATGCTC
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa31811
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 |
---|---|---|---|---|---|
ENSDART00000045971 | Essential Splice Site | 1257 | 1559 | 22 | 28 |
Genomic Location (Zv9):
Chromosome 11 (position 3985050)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 3903554 |
GRCz11 | 11 | 3922941 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTTCTCTCTGTCCGCCAAAGTAGTGGAAGATGAAATCTATTACTTCAGG[T/G]CTGTCAACCTGGTCTATCTACTACTAAACGACTCATCTAAAGAAAAAAAA
Long Flanking Sequence:
TCAAAAACATACATACAGCACCTTTAAAAGCGCATAGTGTGAATTAATTCAGGGCACAAATGTTTCAGTACACTGGAAGATTCTCGAGATGGCTGATGCCCTGTTCAATGCACTGACTACTAAACAAATAGATGATTGACCTTTCAAATGTACGCACATTTCCATCAAGATAATACACATTAAAATATGTAAATGAAAACCTAGCTACTGACTGAAGGAAATTGACTCTAAACTCGGTTATTGACAATGAAAGAACTACTATTACATGAAGTGATTTGTTCAGATCTTTTGTGGACTGCTCTTCCTTTTCCTCAGGGAAGTGTACAGTGTCTTCTTTCAAAGATTTCCTGTCATGCCGGCCGACTGAGATGCCGGAGGAGGACGTGTTGCTGTGTGAGAGCCGCTACATCGAGAGCGAGAAGCAAATGAAGAAGTTTAAAGGGCTGAAGCGTTTCTCTCTGTCCGCCAAAGTAGTGGAAGATGAAATCTATTACTTCAGG[T/G]CTGTCAACCTGGTCTATCTACTACTAAACGACTCATCTAAAGAAAAAAAAAATTGTATACAGCGGGGAAAATAAGTATTGATAAGTGTTGACACAGCCATGTGACAGCTGCTGCGCTCGTGCATCCAGGTTAATCATGAACAACTCAGTGCGCATGCGTTAGTTGCACTATTGCGGTCTGATTATGTTTCAATCAAGGTTTATATGCATCAAATGCATAACATCTGTGCCAAACATTTCAACTGACGAACATATTAACAATAATACAACCGTATAGCCGAATTAAATGTATGCATTGGCATGTTACAGCCCTAATGAGTATGATTATGTGAAACTCCATGTAGATAGATATTGCAATGATTTCGGGTACTTACTTAGCGATGCACGCACACATAACGTTAGATGCACAATCCTTAAATGCTCTGCTGATTTGGACTCTATAATACCTTTTTTATAACTTTAAACTATCAACAACCACTACTATCTTCCCGCTCCGTGGTG
Associated Phenotype:
Not determined