ZMP
brd3b
Ensembl ID:
ZFIN ID:
Description:
bromodomain-containing protein 3 [Source:RefSeq peptide;Acc:NP_997867]
Human Orthologue:
BRD3
Human Description:
bromodomain containing 3 [Source:HGNC Symbol;Acc:1104]
Mouse Orthologue:
Brd3
Mouse Description:
bromodomain containing 3 Gene [Source:MGI Symbol;Acc:MGI:1914632]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa9154 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa1777 | Nonsense | Available for shipment | Available now |
sa2227 | Essential Splice Site | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa9154
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000043638 | Nonsense | 250 | 728 | 7 | 14 |
ENSDART00000050861 | Nonsense | 249 | 662 | 7 | 12 |
ENSDART00000132713 | None | None | 68 | None | 2 |
The following transcripts of ENSDARG00000035126 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 68016604)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 63758103 |
GRCz11 | 5 | 64439267 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GACAACCTGCGCGATCACTGCCAGCCGAAGTGAGTCGCCTACTGCRATGT[T/A]GGAGTCCAAAYACAGTAAAGTCATTTCCAGAYGAGAGAGCACAGGTCGRC
Long Flanking Sequence:
TGAAAATTTGTAGTCTATTAATTAGTTTGATATCTGTAACTTATCCTAGCATAGTGTTTTCCAACCAAGTTCCTGGAGGCACACCAGCAGTACATATTTTGGATGTGTCCTATATCTGATCTATTTATTTCAGGTTTTGGAGTCTTTTCTAATGTTCTGATGAGTTGATTTAGGTGTGTTTGATTAGGGAGAGATTGAAAATGTGTACTGCTGGTATGCCTTAAGGAACAGGGTTTGGAAACACTGACCTAGCGAATGACGGATTGACTTTCTCTAAAGAAGATTACGGTCTAATTAAAAACCCTAAACCAGCCTAAATATCAAGTTTGTCAAGCACACTGCTGAGAAGAATCGTAATTTTTCGTTTCATTGTTTTAATTACGTTCTAACACACCTATGTCATTGTCCTCAGAAGAAAGGGGTGAAGCGGAAAGCAGACACGACCACACCGACAACCTGCGCGATCACTGCCAGCCGAAGTGAGTCGCCTACTGCAATGT[T/A]GGAGTCCAAACACAGTAAAGTCATTTCCAGACGAGAGAGCACAGGTCGACCCATTAAACCTCCCAAGAAGGACCTGGAGGACGGGGACGTCCAGCAGCCAGGCAACAAGAAAAGCAAGCTCAACGATCATCTCAAATACTGTGACACTATCCTCAAAGAGATGCTTTCCAAGAAGCACGCGGCCTACGCCTGGCCCTTCTACAAACCTGTAGACGCGGAGGCCCTGGAGCTGCACGACTATCATGAAATCATCAAGCAACCGATGGACCTCAGCACTGTCAAAGTATGGCCTAAAATTCAACTCACAATTAGTTCCTTTATTAAACAGAAATTAATATGTTGGTATGTATTAATATCTGTAGCTAATTTATATTTAAAACCGGTTGATTTATTGGCATGCTGCTGTGAGCATGTAAGATATTCTGCTGCTGCTGCTGTGTAAATAAGCATTCATAAATCCCATAGCAAATACAAACAGGTGGAGGTGGAAGGTTTCAGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1777
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 |
---|---|---|---|---|---|
ENSDART00000043638 | Nonsense | 261 | 728 | 7 | 14 |
ENSDART00000050861 | Nonsense | 260 | 662 | 7 | 12 |
ENSDART00000132713 | None | None | 68 | None | 2 |
The following transcripts of ENSDARG00000035126 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 68016572)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 63758071 |
GRCz11 | 5 | 64439235 |
KASP Assay ID:
554-1770.1 (used for ordering genotyping assays)
KASP Sequence:
AGTCGCCTACTGCAATGTTGGAGTCCAAACACAGTAAAGTCATTTCCAGA[C/T]GAGAGAGCACAGGTCGRCCCATTAAACCTCCCAAGAAGGACCTGGAGGAY
Long Flanking Sequence:
TCTGTAACTTATCCTAGCATAGTGTTTTCCAACCAAGTTCCTGGAGGCACACCAGCAGTACATATTTTGGATGTGTCCTATATCTGATCTATTTATTTCAGGTTTTGGAGTCTTTTCTAATGTTCTGATGAGTTGATTTAGGTGTGTTTGATTAGGGAGAGATTGAAAATGTGTACTGCTGGTATGCCTTAAGGAACAGGGTTTGGAAACACTGACCTAGCGAATGACGGATTGACTTTCTCTAAAGAAGATTACGGTCTAATTAAAAACCCTAAACCAGCCTAAATATCAAGTTTGTCAAGCACACTGCTGAGAAGAATCGTAATTTTTCGTTTCATTGTTTTAATTACGTTCTAACACACCTATGTCATTGTCCTCAGAAGAAAGGGGTGAAGCGGAAAGCAGACACGACCACACCGACAACCTGCGCGATCACTGCCAGCCGAAGTGAGTCGCCTACTGCAATGTTGGAGTCCAAACACAGTAAAGTCATTTCCAGA[C/T]GAGAGAGCACAGGTCGACCCATTAAACCTCCCAAGAAGGACCTGGAGGACGGGGACGTCCAGCAGCCAGGCAACAAGAAAAGCAAGCTCAACGATCATCTCAAATACTGTGACACTATCCTCAAAGAGATGCTTTCCAAGAAGCACGCGGCCTACGCCTGGCCCTTCTACAAACCTGTAGACGCGGAGGCCCTGGAGCTGCACGACTATCATGAAATCATCAAGCAACCGATGGACCTCAGCACTGTCAAAGTATGGCCTAAAATTCAACTCACAATTAGTTCCTTTATTAAACAGAAATTAATATGTTGGTATGTATTAATATCTGTAGCTAATTTATATTTAAAACCGGTTGATTTATTGGCATGCTGCTGTGAGCATGTAAGATATTCTGCTGCTGCTGCTGTGTAAATAAGCATTCATAAATCCCATAGCAAATACAAACAGGTGGAGGTGGAAGGTTTCAGATAAGACTTTGATAGCATACTGTAGGACCAGCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2227
Status:
F2 line generated
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000043638 | Essential Splice Site | 473 | 728 | 10 | 14 |
ENSDART00000050861 | None | None | 662 | None | 12 |
ENSDART00000132713 | None | None | 68 | None | 2 |
The following transcripts of ENSDARG00000035126 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 68006498)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 63747997 |
GRCz11 | 5 | 64429161 |
KASP Assay ID:
554-2898.1 (used for ordering genotyping assays)
KASP Sequence:
CAATGGTAACAGGGCGGGGACAAAAAACGGGTGTGCCAAACGTTTTCAGG[T/G]GAATGATATTTTTACTTCCCGGTCCCCCACCCCACTAACTCCTCCATTTA
Long Flanking Sequence:
TGAACTTTGAATTAGAACAGGACTTCGGCGACGGTTGATGATGTTTCACGAGGACACAAGAACGCAAGTACAGACAAGAGCGCATTTTGAGAAACAGCCCTAGTGTTTAAATTCAGTAAACAGTGGTGCGTTCAATGAACTGATGACCTTCACGGCCAATCACAGTCATTTCTGTTGAGCACGTGAACACAATGGCAAATCTGCACTGTTTTAATGCACGCTCAACAGCGCTCAATTGTTAGTGGGAAATGAACTTTTAAAAATATCAGTATCAATTGGTACTGAATTCTAGTATCGTGACAACCCTAGTTTCACTATCTCTGTGTCAAACATTTGTGTCGATTTGAAGTTACTCTGCTCTCATGTGACACAGTCTGTTGTTAAAATACATTTTTTTTGTCCCTTGATTTCACTTTGACTTTTTTGCCAGCAATTCGCTGTGGAGCGCCCCAATGGTAACAGGGCGGGGACAAAAAACGGGTGTGCCAAACGTTTTCAGG[T/G]GAATGATATTTTTACTTCCCGGTCCCCCACCCCACTAACTCCTCCATTTATTTTTCGTAGCTTCTTCTTAAGTGAGCGGTAGAGGGTTAAGGTGGTGCTTTTATGGGGTGTATTTAAGCTGGGCATCTCCCTTAAGTCAGCTTGCTTTTGTCACTCAGCTAGTCTTTCGGCTCTGTTTCCCCCTCTCTGCTCTGTGAATGACATTGATTGGCAGGTTTATCGGGGAGAATACCAAATTTATGCCGGGACGTGGTGTCCAGTGCTTCCACATTATCATGGTAGAGCTTTTATTTTCAACGGTTGAAAATAACAATCGAATGAAAGTAGATTATTGTGTTCTTTCAAAATATGATTAATGAGGGGAAAGTGTGCTGGTCTTGGTTTGGATGGAGGCAGATTTTAAAGAGTTTAAATGAATGGAGTTTAAACTAGACTTGAAGCACTGTCATACCAAGAACGATAACTATAAAGAGAATCAAATTAGGGCCCTATGATTTCTA
Associated Phenotype:
Not determined