ZMP

LOC564712

Ensembl ID:

ENSDARG00000086789

Human Orthologue:

BAHD1

Human Description:

bromo adjacent homology domain containing 1 [Source:HGNC Symbol;Acc:29153]

Mouse Orthologue:

Bahd1

Mouse Description:

bromo adjacent homology domain containing 1 Gene [Source:MGI Symbol;Acc:MGI:2139371]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa11391	Nonsense	Available for shipment	Available now
sa36454	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa11391

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
Order Allele From EZRC

Mutation:

T > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000124505	Nonsense	314	812	1	6

Genomic Location (Zv9):

Chromosome 17 (position 31356572)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	31280499
GRCz11	17	31297462

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

GCAGCAGTGCTGCAGCTTCTGTGAGAAGCATGCTCTACACAATGAGGCAT[T/A]ATGGGATGGGAGCACAGGAAGCCATGGCTTTATTAGCCCAGGATATCAGT

Long Flanking Sequence:

GGCCTCTCTGAATGCAGAAGCCGTTAACAGTCTGCTCTTGGACAGAGTAGACCCCCAGCAGACATCAAAACCCTCAAAGAAGCAGCAACAGACAAAAGGAGACCCCTCTCTCTCTAAAGACACTGCTAAAGATAATGATTGTCCCAGAAAAAGCCAAGACAACAGAAAACGGGGATGTACCGGAGAGACCGAACCAAACCGGAATCCCAAAAAAGCGAAGACAGAAAGCGACACTATTGATCTTCAGACTCTAAACAGTCCTGCTCCAAAGCGTCTGGCTGGTTTAAATGCAGCAGCCCTGCTCAAGCTGACCAGCACATCCTCGGCAGGCAAGCGCAGGGGTAAAACAGAAGGCAAACCGAGCGCTGGCGGTGTGCGAGGGAAGCAGCTACTGTCTAAGTCACGTAAACAGCAGCACAACTTGGCCTGTCAGTCTACGTTAAAGGTGTCGCAGCAGTGCTGCAGCTTCTGTGAGAAGCATGCTCTACACAATGAGGCAT[T/A]ATGGGATGGGAGCACAGGAAGCCATGGCTTTATTAGCCCAGGATATCAGTGCAGATCCATGCTCGGCTTTCCCCTGAAGCCTGTGAAGGAAGAGAAAACGGAGACTGATGTGAAATCATATTACTGCTGTTCCCAAGAGAGATCAGTGGAGTACTGCCATAGACTAGCCCTGTTCCTCGGCCAAAAACCCTTCCCGGAAACGGATGAACATTCTCTGAAGGGATTTCTTCCTTCTCCACACACTCTGACGCATTCAGCGATGCCCATCGGTGCCCATCCGTATCCCTGTTACCCTGGTTATTACGTCCACATTGCTCATCATGGGACTCCATCGCTTCCAGTAAGCTCAAACCAAGGAAGCCACCCGCCCTCGTCTGTACCCCCGCTGAAGATGTGCTCTAGCGGAGTCCAGAGACCCAAACTGCTGCCCTCTACGGTGTCCCATCCTACAGGGATCCCTCATCCGGCGTACTGTAACTCTGTGGGCACCTGCTATGGTG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa36454

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:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000124505	Nonsense	329	812	1	6

Genomic Location (Zv9):

Chromosome 17 (position 31356526)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	31280453
GRCz11	17	31297416

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GCATTATGGGATGGGAGCACAGGAAGCCATGGCTTTATTAGCCCAGGATA[T/A]CAGTGCAGATCCATGCTCGGCTTTCCCCTGAAGCCTGTGAAGGAAGAGAA

Long Flanking Sequence:

GTAGACCCCCAGCAGACATCAAAACCCTCAAAGAAGCAGCAACAGACAAAAGGAGACCCCTCTCTCTCTAAAGACACTGCTAAAGATAATGATTGTCCCAGAAAAAGCCAAGACAACAGAAAACGGGGATGTACCGGAGAGACCGAACCAAACCGGAATCCCAAAAAAGCGAAGACAGAAAGCGACACTATTGATCTTCAGACTCTAAACAGTCCTGCTCCAAAGCGTCTGGCTGGTTTAAATGCAGCAGCCCTGCTCAAGCTGACCAGCACATCCTCGGCAGGCAAGCGCAGGGGTAAAACAGAAGGCAAACCGAGCGCTGGCGGTGTGCGAGGGAAGCAGCTACTGTCTAAGTCACGTAAACAGCAGCACAACTTGGCCTGTCAGTCTACGTTAAAGGTGTCGCAGCAGTGCTGCAGCTTCTGTGAGAAGCATGCTCTACACAATGAGGCATTATGGGATGGGAGCACAGGAAGCCATGGCTTTATTAGCCCAGGATA[T/A]CAGTGCAGATCCATGCTCGGCTTTCCCCTGAAGCCTGTGAAGGAAGAGAAAACGGAGACTGATGTGAAATCATATTACTGCTGTTCCCAAGAGAGATCAGTGGAGTACTGCCATAGACTAGCCCTGTTCCTCGGCCAAAAACCCTTCCCGGAAACGGATGAACATTCTCTGAAGGGATTTCTTCCTTCTCCACACACTCTGACGCATTCAGCGATGCCCATCGGTGCCCATCCGTATCCCTGTTACCCTGGTTATTACGTCCACATTGCTCATCATGGGACTCCATCGCTTCCAGTAAGCTCAAACCAAGGAAGCCACCCGCCCTCGTCTGTACCCCCGCTGAAGATGTGCTCTAGCGGAGTCCAGAGACCCAAACTGCTGCCCTCTACGGTGTCCCATCCTACAGGGATCCCTCATCCGGCGTACTGTAACTCTGTGGGCACCTGCTATGGTGAAGCCTGCAGGCTCAGCAGCTATGCCTACAGGCCCACGCAACCCAT

Associated Phenotype:

Not determined