ZMP

brd7

Ensembl ID:

ENSDARG00000008380

ZFIN ID:

ZDB-GENE-040426-2687

Description:

bromodomain containing 7 [Source:RefSeq peptide;Acc:NP_998531]

Human Orthologue:

BRD7

Human Description:

bromodomain containing 7 [Source:HGNC Symbol;Acc:14310]

Mouse Orthologue:

Brd7

Mouse Description:

bromodomain containing 7 Gene [Source:MGI Symbol;Acc:MGI:1349766]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa11332	Nonsense	Available for shipment	Available now
sa7076	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa11332

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
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Mutation:

A > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000100379	Nonsense	55	407	2	11
ENSDART00000143300	Nonsense	55	628	2	17

Genomic Location (Zv9):

Chromosome 7 (position 39136118)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	7	37472758
GRCz11	7	37744016

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

GTCCCGGCCTCGAGACTGCATATGAWGACCAGGTAGATTACGACAAACAC[A/T]AAGATAAGAAANNNAAGAAGAAAAAGAAGGACGAAAAGGACAAAGCCAGT

Long Flanking Sequence:

ACTAATCTGATGTATATGCACAAATATAATATTGTAAAGCTAATTATTAAAAATATGAATTTAAAAGACAGATTTGTGAGGGGTGTACTTATATTTGCTGAGCACTGTATATTTCTTCTCAATAAGACATTTATTATTACTCATAAAATATTACACTCTTCTGTTTTATTTACTAACTAATTATAGCCAGAACAGCAGCAACCAATAAAAAAAGAAAGCAAGTATATTTCCTGAAATAGTGTTAACATTGTGGTTCAGAAAAAGACCCTAGATGTTCATGTTCAATGCAGTGTCTATAGAAATGAATGGGACAGTATTAATATATGGATTGATTATATTACTCTGTAGTTCTTGCATTTGTAAACTGACTTGTGTTTGACAATGCAGAATTTACAGAGCGTCCTCTGAAGCTGGTGTTAAAAGTGGCTGGGAATGAGGTCACTACAGGCAGTCCCGGCCTCGAGACTGCATATGATGACCAGGTAGATTACGACAAACAC[A/T]AAGATAAGAAAAAGAAGAAGAAAAAGAAGGACGAAAAGGACAAAGCCAGTCCTCCAGTATCACCGGTCGACAAAAAGAAAAAGGTGAGAGATCGATGCTGATTTGTTTTGTTCCTTCCTTGTACTGTTTACATAATGCTACATCATATTATCTTGTCTAGATGACCAAAAAAAGAAAGGGCCCAGACCCTGTGGATCCAGACTGGGATGAGCACAGCAGAACTCCCGCTCACTCTGATGTGTCCCAGGACAAGCCTCTGACCCCCTCACTAGCCAAAATGACAGGTAAATCTATGCACGCTTTTATATTTGGGGCCTGATATTGTGTCTTTGCTTAATATGTTAATTATGTCTTTTTGATCCACAGAAAAAGAGCAGACTCCCCTACAAGAGGCTCTAAGTCAGCTCATCCGACAACTCCAGAGGTGGGAATAAATGTTGGCATCTTGAAGTAGGCCTTATAGCTAGGGTGTGAAACATTGATTGTAGGCTGCTTTCAAC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa7076

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:

A > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000100379	None	None	407	None	11
ENSDART00000143300	Nonsense	597	628	16	17

Genomic Location (Zv9):

Chromosome 7 (position 39147141)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	7	37483781
GRCz11	7	37755039

KASP Assay ID:

554-4922.1 (used for ordering genotyping assays)

KASP Sequence:

AGCTGACCAGTCAGGTGACCCCAGCTGATGTGTGCAGTGTTTATGGAATC[A/T]GAAAGGCCATGGGGGTCTCGCTTCCCAATGCACAGGATCCATTCATACAC

Long Flanking Sequence:

GTTTTCCAGCTATTAAACAACAGGCTGATTTATTTATTCCAGTAAAATCTCCTTTTGCTTCCCATAGAAGCAGAGCATTTCCAACAGAAGCTGGATGAGACGACACTGTTGCTGAGGGAGCTGCAGAAAGTTCAGAAAGAGAGACTGAGCGCTAAACAGCCACCAAACATCATCTGTCTGCTGGCTCCCACTGCCAAAGAGCTGCAGCTTGGTAAGAAAACACAAAATGACAGGTTCACTTATCTTTCTCTTTAAGCAGCGTGAGACAAACTCCAACAGTTCTCTTGTCTCTTGAGTTACTTTTTTCTAACTTTTAGGGAAGTCTGCGTTGTTACATATTAACAGATCTGTGGGTTCCAGCAGCTGTTTAAAAGCTGATATACGTGCACATTTCAAATCTAACCCCCACCATTCTTCTTGCAGCGGAGAAAGTCACGGGTAACCTGGCTCAGCTGACCAGTCAGGTGACCCCAGCTGATGTGTGCAGTGTTTATGGAATC[A/T]GAAAGGCCATGGGGGTCTCGCTTCCCAATGCACAGGATCCATTCATACACCTGACCGCAGGTAACATAAGCCCTCTCAGCTCATAAAAGAAACTGCTTCATCCACTCATAAATCGGCATCGAGAGGATAATAACGAATGCTTTTCTGTGTGTTTCAGTGGGAGATCTGATTGAACCCATGGAGGGAGTATGTTGATCCTTCGTCTCTGCAGTATGTCTCTTTCTGCTTAGTCCGGATCCCCCCTTCCTCCAATTTTCATTTGTATTTTGTTCCATTTAAATAAACGTCCTTCTTTTTAAAAAAATATTATTGTGTATTTCTGTTCTTTATTTGTTAAAAAAATTAACGTTAGCATGTGACTAATGCAGAAATAATCTCCTATTGCCTGACTTGTGGCAGAAGGTCTGGACTCCATAATTAATTTGATTAGCCAAAGACCATACAGAGGCGGTCTGACTATTAAGCAAACAAGCACATATTTTGTTGTTGACAGGAATGTA

Associated Phenotype:

Not determined