ZMP
myst3
Ensembl ID:
ZFIN ID:
Description:
histone acetyltransferase MYST3 [Source:RefSeq peptide;Acc:NP_001116784]
Human Orthologue:
MYST3
Human Description:
MYST histone acetyltransferase (monocytic leukemia) 3 [Source:HGNC Symbol;Acc:13013]
Mouse Orthologue:
Myst3
Mouse Description:
MYST histone acetyltransferase (monocytic leukemia) 3 Gene [Source:MGI Symbol;Acc:MGI:2442415]
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa18269 | Nonsense | Available for shipment | Available now |
| sa45191 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa6053 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa2235 | Nonsense | F2 line generated | Not yet available |
| sa45190 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa18269
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 |
|---|---|---|---|---|---|
| ENSDART00000006622 | Nonsense | 352 | 2246 | 5 | 16 |
Genomic Location (Zv9):
Chromosome 5 (position 16118008)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 13913876 |
| GRCz11 | 5 | 14414093 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ARGGGAAGAAAGCTCTTACATGACAAAGCAGCACAAATCAAACGGCGATA[C/A]AATGCACCACTGGGGCGACCGAAGGGCAGGTATTTAATGTTTAATTAWCC
Long Flanking Sequence:
GTATCGAGTGCAAGACCTGCAGCAGCTGCCAGGACCAAGGAAAAAATGCAGTAGGATTATTATTTTTTTTTTGCCACTTCATGCTCTTATTAGATTCTCATTAACTGAATTATTTAAAATAACTCGCAGACTCCTCAGTAAGCATTGTCTTTGTACATTTGTATTTTTACAGGACAACATGTTGTTCTGTGACTCCTGTGACCGAGGCTTCCACATGGAGTGCTGTGACCCTCCACTAACGCGAATGCCGAAAGGTAACTGCCCACACACAATCAAATACATGCCTGCTTTACTTCAGTGTCCAGGGATTATTATTTGTTATATTATTATTATTATTATTAATTGTATATTTGTTTCACAAGGATTGTTTTTCCTTTGTAATTGTACTCTCTAATAATTATTTTTTGATTTTCAGGCATGTGGATCTGTCAGATCTGTCGGCCAAGAGAAAAGGGAAGAAAGCTCTTACATGACAAAGCAGCACAAATCAAACGGCGATA[C/A]AATGCACCACTGGGGCGACCGAAGGGCAGGTATTTAATGTTTAATTATCCTTAAATAACTCAGCAAATGTCTAATTCTCTTCAAATCTTTTAATGAATTTGAAATAAACGAGCATAAGACTACTACGAGTTGTCTTGTCCTCAGACCTGGCCGTCCCTTTAAGAAGATTCGTGGTGGAGGGCGTGGCCGGAGAAGGCGGGGCGCTGGAGGTGTGGATCAGTGTTCACAAGGCTCCTCCTCCCCACACTCTTCCTCAAGCTCCTCCTGCGAAGGTTACCCCGGTGACGATCGCATGCTGTTTTCTCTGAGAGAAGATGACTCTGCACACGGTAGCCTGCGTTTTAACAAGAAAACAAAAGGTTTGATCGATGCCCTCAGCAAGTTCTTCACCCCATCCCCAGATGGCCGGAAAGCCCGTGCTGAAGTGGTGGACTATTCCCAGCAATATCGCATGCGCAAGAAGGGCAACCGGAAAGGCGAGCACGATGACAGGACAGGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45191
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 > G
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000006622 | Nonsense | 486 | 2246 | 7 | 16 |
Genomic Location (Zv9):
Chromosome 5 (position 16115568)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 13911436 |
| GRCz11 | 5 | 14411653 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTTTAACTGTCTTTGTGTCTGTTTGCATCACAGACAATCAGGAGTGCT[C/G]AGACAGCTGGCGGGAGGATGAAGACAAGCTGCCAGGACACGAGAATCTAA
Long Flanking Sequence:
TAAATATAAAACTTGTAGTAATGGTGCTTATAATTGGGGGGTGTGACTAAATTTTGGCAAAAAAAATTAAAGCACCAGTGCTAACAGGCAAAAGGGTTAATTTTGAGCTCTGAAATGCATCGCTGCTGTATTAAAACTATTAATATAAAAGCTTTTTTACCAAAAATTTAGCCGCAGGCTTTTGATTGGAAGTGTATTATGTGGTGCAGTCAGAGATGCTCCTCTGAACAACATAAATAGGGCGTCTGTTTCAGCAACGGCATCACGTTCAGAGTTGTGACAGGACTATTGTAGACATTTGGAGACAGCATAATTGGAAGCTTGACACATCATGCCTGGTTAGGATGCGGTGTAAAATGGAAAAGTACTAATTAAATGTGAATCTGCTGTCTGTTTTGTTGGTGTTTTTGCTCCGGAGACTCAGTTTTCTGCTCACATTCACTCTCTGGCTGTTTTAACTGTCTTTGTGTCTGTTTGCATCACAGACAATCAGGAGTGCT[C/G]AGACAGCTGGCGGGAGGATGAAGACAAGCTGCCAGGACACGAGAATCTAACCGAGAAAGACGTGGAGCTCTTCAGGCACATTCAGGAAATCGCACTACAGGTATGGATCAAGGGAGGGAGAAGTGCCGTTTAATTTGGTCATACAAATTAAAATGACTGATCTAAAGTTAAAGTTACTGGAAAAGTCATGGAATTTTGACAAGGCATTTTTCAGGCCTGGAAAAGTTTTGAGAAAGTAAATAAATCCAAAATGTTTTAAACCTAAAATATCTGTGACTATATTTTGAGATGATAATATTGGGTACATTTTAAATACAAATGCATATTCACTGTAATTCAAGATATATTTTGAGCGTCATGTCCAGATGCGCAAGTCCAACTATAGAAGTTCGATATTGTGGGTATTTTGTACTTTTCTTATAACTCGTGTGTATTTTTACACAGACAGCAGTTTAATTTCTAAATGCATAAAAATAAACTATATAGATACACATAGGCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6053
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 > G
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000006622 | Nonsense | 552 | 2246 | 8 | 16 |
Genomic Location (Zv9):
Chromosome 5 (position 16111437)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 13907305 |
| GRCz11 | 5 | 14407522 |
KASP Assay ID:
554-3845.1 (used for ordering genotyping assays)
KASP Sequence:
GTTATAGAGTTWGGGAAGTATGAAATTCAGACGTGGTACTCTTCCCCATA[C/G]CCACAGGAGTACAGCAGGTAAGCAACATGATGATAATAATGTTGCAGTYA
Long Flanking Sequence:
CATGACATGATCCGAGTGATGCTTCTGCACAAGCTCTTTTACTTACTTTACATTTCTTTGTATATGGAATAAATGAAATGGATTGTATATGTGACTGAGATGCAGAGCAGAGGAGTGTGCGATCACTACTGAGTGTCAGCAGGCTGGCGAGTGGCAGATGCTCTGAATTTCCACTTGGGCTGTGGATAAGAGCTAATAATAATCCCGTAAGCATGAGTGTAATAGAGCTGTATGCTTGTGGGAAACTGTGATTGTTAGAAGAAAGAGAACATGTTTCATGTTTGAAAGAGAGCAACTTTGTGCTTTGTGAAAAGGATATAACACTAGGCCTTGGATTGTCCTGTATTGTAAATTTGTGCTCCATCTTTGCCTCAAGCTATGTTTTTTGTTGTATTCTCACAGAAAGTTGGGGTGACTGGTCCACCTGACCCCCAGATGCGCTGCCCATCAGTTATAGAGTTTGGGAAGTATGAAATTCAGACGTGGTACTCTTCCCCATA[C/G]CCACAGGAGTACAGCAGGTAAGCAACATGATGATAATAATGTTGCAGTTATCAACAACATCATCTCATTGTGTTCAAGATTAGATATATTTCTAACGAATATGGCATGTATTAGGCAAGTTAATTGAATCATATTTTGCCTTTATCTCCCAACTGTTTTTAACAACAACTTCTTCAAAGGGTTGTCCTACATTTACTAGTAAACTTGGATGAGGAATATTTTATTCCCCCATAACAATATTACAATACTTACTGTCTGTGTAACTTTCTAATTAAGTATTGTCAACAATTACTGAGACACAACTGCAAAAACTTAATAAACAGGGAAGATTTATGATAAAATTTAAAAATTAGCAGTACATTTTATAATAATTTTTTAATACTAAAAGACACTATTTTAGTAGAGTTGTTTTGTAGTAAAACTAGGCCTGATTACATTTCAAAAATCAAAAAACACTAGCATAAAGTTTGTAGCATTTTTCCCATATTCATGATTTTATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2235
Status:
F2 line generated
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000006622 | Nonsense | 1464 | 2246 | 16 | 16 |
Genomic Location (Zv9):
Chromosome 5 (position 16101510)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 13897378 |
| GRCz11 | 5 | 14397595 |
KASP Assay ID:
554-3000.1 (used for ordering genotyping assays)
KASP Sequence:
AAAAAAGTGACAGCAGCAGTAGCAGTAAAAGGCGAAAAGGCCAAGACTCT[G/T]AAGATGATGCGGAGGAGCAGGAGGATGAGGAAGATGAGGAACCACCATCA
Long Flanking Sequence:
CTTGTAAAAGGACAGCTAGAGCCTTGATATCTGAAATCAGCCCTGAGAAGCAGAAAGACTCAGAAGATGATGATGATGATTTTCTTCAGGGTTTTAGAGAGTCATCCAGGCCCAAAAAACGAGGTCGGCCACCAAAAAATGCCAACCTCCCTTCCACTGTTCCCAAACCTCCCCCTTTGTCTGAGCCAGAAGAGGAAGATGAGGAGGAAGACAGATGGACCGAGGAAAAGCTTAGCCGTCCACCTTCTCGAACCATGTCACAGTCTTCCAGCTCCAGAGTCCCTCAGCCAAGAGCTAACACAAACATGGCAGATGCAGAGGAAGATGAGGAGCGAGATGATGAAGATTGTAATAACAGGGTCAGTCGGAAAACAGCTACAACACCAGGCTCTGGGAGTCGGCGTAGTGATGACCATGATGCTGATGATGAAGGGGATGGCCGTCTTGAAGAAAAAAGTGACAGCAGCAGTAGCAGTAAAAGGCGAAAAGGCCAAGACTCT[G/T]AAGATGATGCGGAGGAGCAGGAGGATGAGGAAGATGAGGAACCACCATCACCTGCTCACACTCCACCTGTAAAAGAAGAACCCCAGAGCAGTGAGAGTTTTTTAGACATGCAGACTAATGTGGCTCGAGACTATGTCAGCAAACAAGAAGACGGTGACGAAGATGAAGATGATGCAGAGGCAGTGCAGGAGGTGAAGAATAACTCTGCTGATACTGATGAACGCAGGCGCAGAGAGCAAGAGGAATCTGCAGCAGCTGCGGCAGCTGTCGAGACAGTAACTGCAATTGCAGACCCTTCCGAACCAATGGACATGCAGCCTTTACACGTTGAGGACAAAACTGTTCTCATGATGGGGGCTGAGCACTCACACCAGCATCCAGACTTTAAAGATGACCTGAGCCACCAGCAACATACACATCACCACAGTAGTGAGCTGGATCTGGAAACTGTGCAAGCTGTCCAGTCACTCACACAAGGTGAGGCCCAGGAGGAGGATGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45190
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 |
|---|---|---|---|---|---|
| ENSDART00000006622 | Nonsense | 1931 | 2246 | 16 | 16 |
Genomic Location (Zv9):
Chromosome 5 (position 16100109)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 13895977 |
| GRCz11 | 5 | 14396194 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACCAAGTGCCAACCAGCAGCAACAAAAAAAGGTCTCGCAACCCCCTCAA[C/T]AACAACAAAACCCTCAACCACAGCCTCCACCCTCTGCTCCACCACCCCCT
Long Flanking Sequence:
GCTTCAGCGACCTAGGCAGCATTGAGAGCACCACCGAAAACTATGACAATCCAAGCAGCTATGACTCAACTATGGGTGGTGGAGGAAATGGAGGAGGGAATGGAAGTAATGGAGGTGGTATGTCAGCTGCCACCGCAGCAGCGGTGGCTGCTTCCTCTACATCATCTTCATCATCTTCTAGCTCAGCTACACCATCATCGTCATCTTCACAAGGCAACAGCTGCTCCTTTGTCTCAACTCCTGGGTTGACATCCTCGAGCACAGGTGTTGGCTCTCAAATCTCCATGGGAAGTTGTAGCCTTATCCAGCAAACAGGTCCTGGCACAACCAATGGACCGGGTTCTAACAGTACTGGTGGTGTCCCGCAACCTCCACCCCCACCTCCTCCTACTTCTGCCAGCACTCCAACTTGCGGTATAAAGTCTCCACAAGGCTGCGTCATAGAAAGGCCACCAAGTGCCAACCAGCAGCAACAAAAAAAGGTCTCGCAACCCCCTCAA[C/T]AACAACAAAACCCTCAACCACAGCCTCCACCCTCTGCTCCACCACCCCCTCCACCTCAACAGCAAGCCCTCTCACAGTGCAGCATGGGAAACGGCTTTGCTTCCATGCCCATGATTATGGAGATTCCTGAAAGTGCAGGCAGCGGTGGAGGAGGTCGGAGTTTGTATGATCGAATGGGCCAGGACTTCGGTGCTGGTGGTTACAGTTTAGCCAAACTCCAGCAGCTAACAAACACTATCATGGACCCCCATGGAATGTCTTATTCGCATTCAGCTGCAGTCACCTCATATGCGACAAGTGTTTCACTGTCTAACCCAGGGTTAGCGCAGCTTGCTTCTTCTCCACACCCACCTTTGGGCCAGGCTCAGCCCACAATGACTCCACCTCCCAATTTGGGTTCTGGGTCTATGAACCTTGGGTCTCCCTTAATTCAGTGCAACATGACGGGCGCTAACATCGGACTACCTCCCACTCCCCATCCACAACGGTTGCAAGGCCAA
Associated Phenotype:
Not determined