ZMP

brd3a

Ensembl ID:

ENSDARG00000006527

ZFIN ID:

ZDB-GENE-030131-6141

Description:

bromodomain containing 3a [Source:RefSeq peptide;Acc:NP_001116861]

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 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa37272	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa45732	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa37272

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:

T > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000026708	Essential Splice Site	222	683	None	13
ENSDART00000126672	Essential Splice Site	222	514	None	11
ENSDART00000130597	Essential Splice Site	222	498	None	10
ENSDART00000135239	Essential Splice Site	222	683	None	12

The following transcripts of ENSDARG00000006527 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 21 (position 16890503)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	21	18235452
GRCz11	21	18272088

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGCTGCCGCTGTGATACCCAGCATGCCTCCATCACAACCCACGGTTAAAG[T/A]AAGTCACATGACTTCTCTGGACGTCACATGACATATTTAGTGTCGTTGCC

Long Flanking Sequence:

AGACTAGTTTAAAACACAGTTTTGAGACAGAGGAAGCTTAGACAATTAATGTATATATTTTTATTTGTTTTCTTAGCCAACGGATGATATTGTGTTGATGGCACAAGCGTTAGAGAAGATCTTCCTTCAGAAAGTGGCCCTCATGCCCCAGGAAGAGGTTGAGCTGCTTCCACCTGCCCCGAAGGGCAAAGGGCGCAAACCAGCAGGGCCTGGTAAAATTGAAATCAGCTGAATGAAGAATTAATTATAACATCCTATATTCATGCATAATAAATAATATTATTTTCCTCCTAATTATTTAAATGCAGGTCAGCAAGATGGAGCCGTCTCCACTGGCTCACCCACATCAGTTTTTCCAGGTGCCACATCGCCGAGTTCACAAACAGCAGTAGTATCTCCAGCTCCAGTGCCCGCTATCACTCCTAGCATACCAGCTGTACAGAACACAACTGCTGCCGCTGTGATACCCAGCATGCCTCCATCACAACCCACGGTTAAAG[T/A]AAGTCACATGACTTCTCTGGACGTCACATGACATATTTAGTGTCGTTGCCTCACCACCGGCTTTGTGTTTCCCCATTTGTGGTTTTTTGGTTTTCCTAGAAGAAAGGGGTAAAGAGGAAAGCAGACACAACCACCCCTACTACCTCTGCTATCACCGCGAGCAGAAGCCAATCACCCACCCCAATTTTAGAAGGCAAGCAGAGCAAGGTGGCAGCCCGGCGAGAGAGCACCGGTCGCCCAATTAAACCACCTAAAAAGGATTTTGAGGATGGTGAACTAGGCGTGCATGGTGGCAAAAAGGGCAGACTTTCAGAACAGCTTAAGTACTGCGATGTCATCCTTAAAGAAATGCTGTCAAAAAAACATGCTGCGTACGCTTGGCCATTTTACAAACCTGTTGATGCAGAGGCTCTCGAGCTGCATGACTACCATGATATAATCAAACACCCCATGGACTTAAGCACAGTAAAAGTATGTTGAGTTTGGACACTTAGCTGTTA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa45732

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
ENSDART00000026708	Nonsense	449	683	9	13
ENSDART00000126672	Nonsense	448	514	9	11
ENSDART00000130597	Nonsense	449	498	8	10
ENSDART00000135239	Nonsense	449	683	8	12

The following transcripts of ENSDARG00000006527 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 21 (position 16891472)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	21	18234483
GRCz11	21	18271119

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CCACCTCTGACAGCTCCGACTCTGAGGAGGAGAGGGCCACCCGGCTTGCC[G/T]AGCTGCAGGAACAGGTGGGTGCGGAACAGGTGGGTTTCAAAACAAGGACC

Long Flanking Sequence:

AAAGTATGTTGAGTTTGGACACTTAGCTGTTATAATGCCTTCAGTTTTACAAGGTAATATTCATGTTTATTTTCTTGCCTGCTTACAGAAAAAAATGGATAGTCGAGAGTACCAGGATGCTCAGACTTTTGCTGCAGATGTGCGATTAATGTTCTCAAATTGTTACAAGTACAACCCACCTGATCATGAGGTGGTTGCTATGGCCAGAAAACTGCAGGTGAGTCGTTGTTGTATTGCCTTCTCCATTTGACAATTACGTTCCCTTTGTTTAAATCAAAACTCTTATTAGAATATAGTGACGTTTTGCTTGTTATTCTTTCCAGGATGTGTTTGAAATGCGATTTGCAAAGATGCCTGATGAGCCAGTGGAGGTTCCTGGGGCAGGTGGTGTAGGTGGGGCCGGTGTGGTCAGTAAGAGTACTGTCAGCAGTGAGAGCAGTGGCGACTCCTCCACCTCTGACAGCTCCGACTCTGAGGAGGAGAGGGCCACCCGGCTTGCC[G/T]AGCTGCAGGAACAGGTGGGTGCGGAACAGGTGGGTTTCAAAACAAGGACCAAGTTCCTTTATCCTCTCCAGGCTCAGAGATGTTCTCAGGCCACATGAAATGTCTCAACCTTTTTACACCTCACGCACATGCCATTCTTAATCAATGCTTATTCTCTAAAAAACCTGGAAGGCTTCCACTTTTACAGCAGCACCTTTTTGCTTTCAACTTGTGCACTTGTACAAAGAGCTGTTTTTTTAGCCCTCTACCGCGACCAGCTGCATATATTGGTTTGCATTTTAATCTCAAAATGCCTGGATGTAGATGTAGTATCATTTATGTTGTTTTGTTTCTGTCTTATTGGAGCTCTATATCACATTTTCTTCCCTTGCCATTTTTTTTTTACCAGTGTATCTCTTTGGAGCACCCCATTGGTAGCAGAAAGGGGATAAAAAACGGGTGCACCAAGAATAATCAGGTGATTTCACATTTCCCTGTCCCTGCCTATGAACATTGTGTAT

Associated Phenotype:

Not determined