ZMP
LOC557210
Ensembl ID:
Human Orthologue:
BACH2
Human Description:
BTB and CNC homology 1, basic leucine zipper transcription factor 2 [Source:HGNC Symbol;Acc:14078]
Mouse Orthologue:
Bach2
Mouse Description:
BTB and CNC homology 2 Gene [Source:MGI Symbol;Acc:MGI:894679]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa42898 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa23029 | Nonsense | Available for shipment | Available now |
sa11743 | Nonsense | Available for shipment | Available now |
sa28828 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa42898
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000019017 | Nonsense | 368 | 727 | 3 | 6 |
Genomic Location (Zv9):
Chromosome 17 (position 15563501)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 15714329 |
GRCz11 | 17 | 15722262 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTCTCTCAAATCGCTTTCTCTTGAGAGGATTTGTTCACAAGATCCCGAA[C/T]AAGAGAACGACAGAAAAAGTGTCATCTTTTCCTCTCGAGGCCCCTACCAT
Long Flanking Sequence:
CGCACAGCAGTACCTCAAGCTTACAAGGCTCCCTGCAGGACACCGTCACCAGCAGCAATGCCCGAGGCCTGGATCTCTCCAAGGTAAAAGCAGAACCAGTCAATGGGGAAGTCTCTGTGCCGTTAGACTTGTCTGAGTTGGAACAGAATGGTCCGGTCAGGGGTAAAGTAATTGAGATGGACATAGAAATGGAGTTTGATGGAAGGCAACTTAGTTCAACACCCAATGAATTCCCAGCAAGCAAACGATCACCGGTGTGCCTGCGCTCCCTTGTTAAAAAGGAAGTCTCATCTTCAGATCATTGTCTTTCCACTGACCTGCAGCTTTCCAGCAGAACTTCTCCACTTCGGGAACAACAGGTTGTCACAGTTCAGGAACAACAGGTTGACTTCCAAAAGGACTATCAGGCTTTTATTGGAGGACTCTCGTCAAAGAAATTACCCGATGGAGTGTCTCTCAAATCGCTTTCTCTTGAGAGGATTTGTTCACAAGATCCCGAA[C/T]AAGAGAACGACAGAAAAAGTGTCATCTTTTCCTCTCGAGGCCCCTACCATTTGGCGCCCACACATTCATATCCTGATGAGAGTTGTTTGGGGCAGGAGACTCCAGAAGACCTGTGGGCAGGATCCAGCCAGTCGTTTCCCTGCACCCAAACTCTGTCCCCAACTTCGTCCTCTCAAGATCCCTCTTTGCCCTATCGCCGGCACCCTAAGAGCAGTTGTCCGGTGCCCATTAAAATGTGTTCCCGCTCGACTCGTGCCGATAGCCATGTCAGAACCTCCAGCTCATGCTCTTCCTACTCGTATGCAGAGGACGGCAGTGGAGGCTCTCCTTCCAGCCTGCCCCAGTTCGAGCTCTCTACCTCTCCTTGTTCCACCATGGCGCGTTGTCTGGCCCTCGAACACCGGGAGCATAGCACGTCGGGGCCACCAAAAATCAAGTGCGAGAAGTCATACGACACTAATTCCAGTGACGAATCTGGATCTTTTTCTGATGGCGATAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23029
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000019017 | Nonsense | 390 | 727 | 3 | 6 |
Genomic Location (Zv9):
Chromosome 17 (position 15563568)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 15714396 |
GRCz11 | 17 | 15722329 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGTGTCATCTTTTCCTCTCGAGGCCCCTACCATTTGGCGCCCACACATT[C/A]ATATCCTGATGAGAGTTGTTTGGGGCAGGAGACTCCAGAAGACCTGTGGG
Long Flanking Sequence:
CCTGGATCTCTCCAAGGTAAAAGCAGAACCAGTCAATGGGGAAGTCTCTGTGCCGTTAGACTTGTCTGAGTTGGAACAGAATGGTCCGGTCAGGGGTAAAGTAATTGAGATGGACATAGAAATGGAGTTTGATGGAAGGCAACTTAGTTCAACACCCAATGAATTCCCAGCAAGCAAACGATCACCGGTGTGCCTGCGCTCCCTTGTTAAAAAGGAAGTCTCATCTTCAGATCATTGTCTTTCCACTGACCTGCAGCTTTCCAGCAGAACTTCTCCACTTCGGGAACAACAGGTTGTCACAGTTCAGGAACAACAGGTTGACTTCCAAAAGGACTATCAGGCTTTTATTGGAGGACTCTCGTCAAAGAAATTACCCGATGGAGTGTCTCTCAAATCGCTTTCTCTTGAGAGGATTTGTTCACAAGATCCCGAACAAGAGAACGACAGAAAAAGTGTCATCTTTTCCTCTCGAGGCCCCTACCATTTGGCGCCCACACATT[C/A]ATATCCTGATGAGAGTTGTTTGGGGCAGGAGACTCCAGAAGACCTGTGGGCAGGATCCAGCCAGTCGTTTCCCTGCACCCAAACTCTGTCCCCAACTTCGTCCTCTCAAGATCCCTCTTTGCCCTATCGCCGGCACCCTAAGAGCAGTTGTCCGGTGCCCATTAAAATGTGTTCCCGCTCGACTCGTGCCGATAGCCATGTCAGAACCTCCAGCTCATGCTCTTCCTACTCGTATGCAGAGGACGGCAGTGGAGGCTCTCCTTCCAGCCTGCCCCAGTTCGAGCTCTCTACCTCTCCTTGTTCCACCATGGCGCGTTGTCTGGCCCTCGAACACCGGGAGCATAGCACGTCGGGGCCACCAAAAATCAAGTGCGAGAAGTCATACGACACTAATTCCAGTGACGAATCTGGATCTTTTTCTGATGGCGATAGCGAGTCGTTTGCCACCAAAGAGCGCACACAAGAGGTTAGTGTACACTGCTAAAACAGAAATGTGTAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11743
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000019017 | Nonsense | 432 | 727 | 3 | 6 |
Genomic Location (Zv9):
Chromosome 17 (position 15563695)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 15714523 |
GRCz11 | 17 | 15722456 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
WCCCAAACTCTGTCCCCAACTTCGTCCTCTCAAGATCCCTCTTTGCCCTA[T/A]CGCCGGCACCCTAAGAGCAGTTGTCCGGTGYCCAWTAAAATGTGTTCCCG
Long Flanking Sequence:
TTTGATGGAAGGCAACTTAGTTCAACACCCAATGAATTCCCAGCAAGCAAACGATCACCGGTGTGCCTGCGCTCCCTTGTTAAAAAGGAAGTCTCATCTTCAGATCATTGTCTTTCCACTGACCTGCAGCTTTCCAGCAGAACTTCTCCACTTCGGGAACAACAGGTTGTCACAGTTCAGGAACAACAGGTTGACTTCCAAAAGGACTATCAGGCTTTTATTGGAGGACTCTCGTCAAAGAAATTACCCGATGGAGTGTCTCTCAAATCGCTTTCTCTTGAGAGGATTTGTTCACAAGATCCCGAACAAGAGAACGACAGAAAAAGTGTCATCTTTTCCTCTCGAGGCCCCTACCATTTGGCGCCCACACATTCATATCCTGATGAGAGTTGTTTGGGGCAGGAGACTCCAGAAGACCTGTGGGCAGGATCCAGCCAGTCGTTTCCCTGCACCCAAACTCTGTCCCCAACTTCGTCCTCTCAAGATCCCTCTTTGCCCTA[T/A]CGCCGGCACCCTAAGAGCAGTTGTCCGGTGCCCATTAAAATGTGTTCCCGCTCGACTCGTGCCGATAGCCATGTCAGAACCTCCAGCTCATGCTCTTCCTACTCGTATGCAGAGGACGGCAGTGGAGGCTCTCCTTCCAGCCTGCCCCAGTTCGAGCTCTCTACCTCTCCTTGTTCCACCATGGCGCGTTGTCTGGCCCTCGAACACCGGGAGCATAGCACGTCGGGGCCACCAAAAATCAAGTGCGAGAAGTCATACGACACTAATTCCAGTGACGAATCTGGATCTTTTTCTGATGGCGATAGCGAGTCGTTTGCCACCAAAGAGCGCACACAAGAGGTTAGTGTACACTGCTAAAACAGAAATGTGTAAAATTTACAGTAAAAAACTGACTGCCGTGGTTTCCAAAATGTTACCTTTAATAATTCTGGGAACCACATATACCAGTTTTTTGTTTGTTTGTTTTTTTAACTGTTAATATTTAAGTATGAGAATCAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa28828
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:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000019017 | Essential Splice Site | 467 | 727 | 3 | 6 |
Genomic Location (Zv9):
Chromosome 17 (position 15563800)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 15714628 |
GRCz11 | 17 | 15722561 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTCGTGCCGATAGCCATGTCAGAACCTCCAGCTCATGCTCTTCCTACTC[G/T]TATGCAGAGGACGGCAGTGGAGGCTCTCCTTCCAGCCTGCCCCAGTTCGA
Long Flanking Sequence:
CATTGTCTTTCCACTGACCTGCAGCTTTCCAGCAGAACTTCTCCACTTCGGGAACAACAGGTTGTCACAGTTCAGGAACAACAGGTTGACTTCCAAAAGGACTATCAGGCTTTTATTGGAGGACTCTCGTCAAAGAAATTACCCGATGGAGTGTCTCTCAAATCGCTTTCTCTTGAGAGGATTTGTTCACAAGATCCCGAACAAGAGAACGACAGAAAAAGTGTCATCTTTTCCTCTCGAGGCCCCTACCATTTGGCGCCCACACATTCATATCCTGATGAGAGTTGTTTGGGGCAGGAGACTCCAGAAGACCTGTGGGCAGGATCCAGCCAGTCGTTTCCCTGCACCCAAACTCTGTCCCCAACTTCGTCCTCTCAAGATCCCTCTTTGCCCTATCGCCGGCACCCTAAGAGCAGTTGTCCGGTGCCCATTAAAATGTGTTCCCGCTCGACTCGTGCCGATAGCCATGTCAGAACCTCCAGCTCATGCTCTTCCTACTC[G/T]TATGCAGAGGACGGCAGTGGAGGCTCTCCTTCCAGCCTGCCCCAGTTCGAGCTCTCTACCTCTCCTTGTTCCACCATGGCGCGTTGTCTGGCCCTCGAACACCGGGAGCATAGCACGTCGGGGCCACCAAAAATCAAGTGCGAGAAGTCATACGACACTAATTCCAGTGACGAATCTGGATCTTTTTCTGATGGCGATAGCGAGTCGTTTGCCACCAAAGAGCGCACACAAGAGGTTAGTGTACACTGCTAAAACAGAAATGTGTAAAATTTACAGTAAAAAACTGACTGCCGTGGTTTCCAAAATGTTACCTTTAATAATTCTGGGAACCACATATACCAGTTTTTTGTTTGTTTGTTTTTTTAACTGTTAATATTTAAGTATGAGAATCAAAATGTACACAATTTACACAATTGGTTTTATTTCAAAGATTCACAGTAAACTACCATACTTTATTAGTTAATTTGATTGTTATACACTAGTCTTTTCAAGTATTAATA
Associated Phenotype:
Not determined