ZMP
myst2
Ensembl ID:
ZFIN ID:
Description:
histone acetyltransferase MYST2 [Source:RefSeq peptide;Acc:NP_997800]
Human Orthologue:
MYST2
Human Description:
MYST histone acetyltransferase 2 [Source:HGNC Symbol;Acc:17016]
Mouse Orthologue:
Myst2
Mouse Description:
MYST histone acetyltransferase 2 Gene [Source:MGI Symbol;Acc:MGI:2182799]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa38873 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa45448 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa38873
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000004896 | Nonsense | 139 | 568 | 4 | 15 |
| ENSDART00000142659 | None | None | 102 | None | 3 |
The following transcripts of ENSDARG00000031770 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 12 (position 6677593)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 12 | 5960513 |
| GRCz11 | 12 | 5994097 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCAGCGATCCCTCTCATCGGCCAAAACGCCGCCGCTTTCATGAGAGCTA[C/A]AACTTCAATATGAAGTGCCCCACACCTGGGTGCAATTCTCTGGGTAATTG
Long Flanking Sequence:
TTGAAAAATAAAAAAACATATGTAAAAAAAAAGTACCATGTTTTGTAAGCAGCAAGCCAACTTTTAATATAGGTTAAAAAAGAAAACCAAAATACAAACTGTGTAAATCAGAATGAGACTGAATTCTTCAAGGGTGACGCGTTTCTTTTGTTTAAAGCAAAAGAACATATTTTCACATTATATACACATGCTTTATAGTAACAAAATGATTGTCCTTATGATTATTTTATTTTACTTATTATTTATAGTTTTTGCACATTTATACTTATCATAAGAAATGAATTTATTCTTCATCTAGATGCTCCACCCGATATAAAGCAAGCAGTGGAGCGAGATGAGTCTCCTCCCAGGACGCCAACAGGAAACGCCCCGTCGTCTGAATCAGACATCGACATATCCAGCCCCAACGCATCCCACGATGAGAGCGTGACTAAAGACCAGAAAGACTCTGGCAGCGATCCCTCTCATCGGCCAAAACGCCGCCGCTTTCATGAGAGCTA[C/A]AACTTCAATATGAAGTGCCCCACACCTGGGTGCAATTCTCTGGGTAATTGCTCTTCAGATTAATTTCCTGTTGCATCTGCTTAATAATCATTTTCAGTGCTAATTGTTTACAAGGGCTTAATTGGGAAAAATAAACATTTAAATGTTACTGGATCGTTTATGATGAAATATGAATATTGTTCTGTTTTTTTTTTTTTTTGTTCTTTTGCACAGGACATTTAACAGGTAAACATGAGCGCCATTTCGCCATTTCAGGATGCCCTCTCTATCATAACCTCTCTGCAGATGAATGCAAGGTATGTTAAGGGCAAAATATGTTTGGCTTGTTTGTGTTTTATTATTTTCTGTTATTAAGACACTGCAGGTAAATAGGGTAAAATGGAATTAATTATCATCACTGACATTCTTCAGTGTATTAAGTACACTTTTTGAGTGTAATTTTTGTGAAGAGTTGGGAGTTTTTATTATTTGATAATGACATTTTTTTTTTATTAAATATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45448
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 |
|---|---|---|---|---|---|
| ENSDART00000004896 | Nonsense | 394 | 568 | 11 | 15 |
| ENSDART00000142659 | None | None | 102 | None | 3 |
The following transcripts of ENSDARG00000031770 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 12 (position 6670847)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 12 | 5953767 |
| GRCz11 | 12 | 5987351 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACCTCTGCTTGCTGGCCAAGCTGTTTTTGGACCATAAAACACTGTATTA[T/A]GATGTGGAGCCTTTCCTGTTTTATGTCATGACTGAAGCTGATAACACAGG
Long Flanking Sequence:
CCAGAGGAATATGCCCGTCTGGGGCGACTGTATGTCTGTGAGTTCTGCCTCAAGTACATGAAGAGCCAGACCATCCTGCGCAGACATATGGTATGAAGTAATAGTAACCTCTGCTATGGCTTGAGTTTAGTCAGATGTTTGTATTGGAGGCATGTTTATAAAGGTGAAGTTAAGTTTGACATTTTCATTTGTATGTCATCTCTACAGGCCAAATGTGTGTGGAAACATCCTCCAGGGGATGAAGTCTATAGAAAAGGTGCCACCTCTGTGTTTGAGGTTGATGGAAAAAAGAACAAGGTGGGCAATGAATTCAAAATGACTCTTACGTTTGGGATATATCCGTTTTTTTTTGTGTGTGGCAGTTTTCACTTCTAAATTAAATTCTATGTTAACTCGCTACATATGAAGCTGATTTCTTTCATCCATGTGTCTCAACAGATCTACTGCCAGAACCTCTGCTTGCTGGCCAAGCTGTTTTTGGACCATAAAACACTGTATTA[T/A]GATGTGGAGCCTTTCCTGTTTTATGTCATGACTGAAGCTGATAACACAGGCTGTCACCTTGTGGGATATTTCTCAAAGGTAATGCAGTGGTGCAGTCTATGGAAACTCACTTAAACTGAAATTTATTATAACATTACATATTTTCACAATACTTGCATTTAAGGTAAAATTTTGGGCAGATTTTTAATCATAAGCCTCTTTTGTTGAGACACTGCTCGCTGCAGAGCCACTTGGGCTCCAGTGAGGGGGAGCTTGAGCTCCAACTCCTCCTCCTATAAGCTGTTTTAATGCGTACATCCACCCCTAACCGCAACCCCCAGTGACATCACTTGTAGAAGAAGTGCAAGGAAGGAGGAGCTGGAGCTCAAGCTCCCCCTTGCTGGAGCTCAGCTCTGCCCACATGGCTCTGCAGTGAGCACCACTTGCTTTCGTTTACGCTCAGGCTATGGTAGTGCTGTTCAGAGAACATCAAACTTGTTGAAATGATTTGAAGACTGGAT
Associated Phenotype:
Not determined