ZMP
pbrm1l
Ensembl ID:
ZFIN ID:
Description:
Polybromo 1, like [Source:UniProtKB/TrEMBL;Acc:Q4KM18]
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 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa20804 | Nonsense | Available for shipment | Available now |
sa33952 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa20804
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 |
---|---|---|---|---|---|
ENSDART00000064868 | Nonsense | 7 | 449 | 2 | 12 |
ENSDART00000103472 | None | None | 454 | None | 7 |
ENSDART00000131203 | Nonsense | 7 | 1648 | 1 | 30 |
ENSDART00000132845 | Nonsense | 7 | 1575 | 2 | 29 |
ENSDART00000138567 | Nonsense | 7 | 1629 | 2 | 30 |
The following transcripts of ENSDARG00000077038 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 6 (position 46346785)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 46407719 |
GRCz11 | 6 | 46409601 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTTTTGGATTATTGGAACAGGTACTGTCTCAATGGGCTCCAAGAGAAGA[C/T]GAGCCACCTCTCCCTCCAGCAGTGCCAGCGGAGGAGACTTTGACGATGCC
Long Flanking Sequence:
ATCTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAATAAATAGTATAAGGCACAACAAATGTATTATATATGGATACAAATGTATATTTATATGTTAATAATTAAAAGTTTAAATGAACATTTCATACTAATATTTTAGAGAAAATGACAGACAGGTAGGCCTTCAAAAATTGCTCAGAGAAAGAATTGCGCCCCGAAGTGAAAAAGGTTAAGAACCCCTGCTCTATATGACAAGTTTTTTTTTTATTTTAAATTTGGATTAAATTTAATTTAAGAATGAAAATAATGCAGTTTACACAAACACAACTAAATTGCAAATCAATAAAACTTTCAAGTGATTTCTTAATATTTTGCATAGCTGTAGGATTCATTAGTCACAAGTTGTGAAAATCCTGCATCTGAAAGGATATGTTTTTGGATTATTGGAACAGGTACTGTCTCAATGGGCTCCAAGAGAAGA[C/T]GAGCCACCTCTCCCTCCAGCAGTGCCAGCGGAGGAGACTTTGACGATGCCAGCTCATCCACGCCAGTCAGTGGATGGAAGAGGAGGAGAGCCTCCAATGCTCCTTCTGTTGATCAAGTGAGTACATGGGGTTTAGTATGTTAATTAATATTTTACTAAGCACCCATTACTGGTTTTGGCAGTTTGTTTACCTTAACTGTATCCTGCCTTTAGATTGCTGTGTGCCATGAATTGTACAACACTGTTAGAGATTATAAAGATGATCAAGGCAGACAGATCTGTGAGCTCTTCGTTCGTGCACCAAAGAGGAGGTATGAGTGTATTCCTTATCTTTAGTGTACACTGAATGATGATAGTGGTTTGTTTCACTGTTTGGTTATTTGAAGGTGGTTAAAAGAGGTACAACTCTAAATGTTTTACATCCTGCTAATGCCTGCATTTATAATTACAATTGTGCATAGATTGGATATAATGAACAAGTAAAGAAAAAATAAAAAATAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33952
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 |
---|---|---|---|---|---|
ENSDART00000064868 | Nonsense | 183 | 449 | 6 | 12 |
ENSDART00000103472 | None | None | 454 | None | 7 |
ENSDART00000131203 | Nonsense | 183 | 1648 | 5 | 30 |
ENSDART00000132845 | Nonsense | 183 | 1575 | 6 | 29 |
ENSDART00000138567 | Nonsense | 183 | 1629 | 6 | 30 |
The following transcripts of ENSDARG00000077038 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 6 (position 46348243)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 46409177 |
GRCz11 | 6 | 46411059 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGATATTTTTCCCTGTGTACATTTGTAATTAACAGAGACCACCAAGCTA[T/G]TTAAAAGCCATACTGGAGCAGCTCTTGGAGGCCATCGCATCCTGCACTGA
Long Flanking Sequence:
AGTTTTCAGCTGACTTTCATCTGCTAATTAATAACACCAAAGCTTACTATCAGGTAAGTTTGCACGTAAACATTTAAGTCCATTAATTATTGATGTTTCTGCCACATGAATAAGCTGAGTCTGTCTTTTATTTTATGCTACGAATGCACATGCAAAGTTGCTCAACATCAAAACAATTCAGAAACACTAATATTCCTCTTATGTTCTCTAACAACAGGCTGACAGTGCAGAGCACAGAGCGGCATCTAAGCTTTTGAACGTCTTCCTATCTGCCAAGAATGAACTGCTGCAGGGTGGGGATGGAGAAGAGGCTGAGGATGATGAGGAAAGTGAAGATGCGGAGAACACAAACGCTTCTATGGAGGAGGAGGTAAAGAAAATGCACTGACAGATGTAGACCTTCAGTATTTTTTTTTTTTAAGATTTCAGTCCATAGACATCCAGACTGATATGATATTTTTCCCTGTGTACATTTGTAATTAACAGAGACCACCAAGCTA[T/G]TTAAAAGCCATACTGGAGCAGCTCTTGGAGGCCATCGCATCCTGCACTGATTCCTCAGGGAGGCTTGTTAGTGAGCTCTTCCAAAAACTTCCTTCCAAACTGGTAAGACCCAAGCGTGTGCACTTGATTCAAATCAGACTAATTTGTTACTTTCATAAAACCTAGTTTAGGTTGGATTTTTAGTGATAAATGTTGTTTATTTTCATTGATTAATTTTTCTTTTGTTTGTTTCAGCATTATCCAGACTACTATGCTGTCATAAAAGAGCCAATAGACCTACGCGCTGTGGCTCAGAAGATCCAGGTATTGAAAACACAGTAGCTTAATGTAGCAATATAAACTTGCTGTAATGTGTGTTTGGAGATGTTATGTTGTAAAATTTCAGAGGCTGTTTATGTAAAATATCTTCAATTGTACATATTGATATGCAGTAAATAATAACACTTCTCAACCAAATTTTCATGAGATGATAAGTATTATAACATGTTAGCATCTTTATT
Associated Phenotype:
Not determined