ZMP
si:dkey-24f15.3
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate MYST histone acetyltransferase (Monocytic leukemia) 4 (MYST4) [S
Human Orthologue:
MYST4
Human Description:
MYST histone acetyltransferase (monocytic leukemia) 4 [Source:HGNC Symbol;Acc:17582]
Mouse Orthologue:
Myst4
Mouse Description:
MYST histone acetyltransferase monocytic leukemia 4 Gene [Source:MGI Symbol;Acc:MGI:1858746]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa14848 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa42204 | Essential Splice Site, Splice Site | Mutation detected in F1 DNA | Not yet available |
sa16535 | Nonsense | Available for shipment | Available now |
sa15696 | Nonsense | Available for shipment | Available now |
sa1676 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa14848
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 |
---|---|---|---|---|---|
ENSDART00000077775 | Nonsense | 541 | 2043 | 6 | 16 |
ENSDART00000136624 | None | None | 1368 | None | 10 |
ENSDART00000148191 | Nonsense | 541 | 646 | 6 | 6 |
Genomic Location (Zv9):
Chromosome 13 (position 25105479)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 24751139 |
GRCz11 | 13 | 24881589 |
KASP Assay ID:
1641-0498.1 (used for ordering genotyping assays)
KASP Sequence:
AGCKWAAGGGACTCTTTGATGGACTGTCTCACATYTTTACCACTCAGGGA[C/T]AGTCCCGACAAAAGGGACTCCCCAGCTACGCACCACCCAAGCGAGTGCGC
Long Flanking Sequence:
GTTCCATAAGCACTTTCTGTACCCCACCCTCATCAAGCACCTTTATACCCACCACAGACGGCAGGAGTCTCACTGACCCCCTCACATCCACACCCACCCTCACTACGTTGCCCCCAATCAACAAGAAAACCAAAGGTCTCATTGACGGGCTTTCCAAATTTTTCACGCCATCGCCCTTGGGTCGCCGGTTGCGCGGTGAAGCGTCGGGCTCCTCGAATCAGCACAGGCCAAGGAAACGGGGCTATCGGAAACACCATGCCAGCATGATGACACCAGGTGTGAGGTTAAACGCCCCGTCTAGCGTTCTCCTTACCCCGTCCCCTTCGCAAGGACACAGCCCCATCTCGCTGAACCCCACCCAATCATCCTCGCCCTCCTCCGCCCACTCGCCCCACAGCTCCTCCTCCCAATCTAGTGGCCCGTCCCTTAGTAGCCTCCCAGGCAACAGCCAGCTAAAGGGACTCTTTGATGGACTGTCTCACATCTTTACCACTCAGGGA[C/T]AGTCCCGACAAAAGGGACTCCCCAGCTACGCACCACCCAAGCGAGTGCGCCGCACACAGGACATGTCCACCTCACCCAAAATGTCCCTGCAGCTTCAAGGAAAGAAGCCTGTCAAGGGTTTCTGTAGTAAATTAGCATCTCTGGCCAGTTCAGCCTCAGGATGGCCGCCCAAGCGGGGCCGCCCGTTTAAGTCGGCGCTCCATTTCAAACGAACTCCCATCTTGAGAAAGCACAAGCTGCTAGGCAGGTTTAGGTTTAAGGCCTCCCCGCAGAGGGAGAACATCACACCAGGGAAGGGCAGATTGGCAGACGGACGAGTTAAACCAGACCCAAACCATGGTAAGCACAGGCGCCTGAACCTCCAAACGGCCGACTAGCTTTTTCCATCTTAAACCGTTTTACTCATCTTCCTCATTTTTAGAAGCAAAATAACATGGATTTTTGTTTTCCAACTAATACTGCATCTCAGCATTTTTGTTTTTAACCTTTTTCTTCAGTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42204
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 > A
Consequence:
Essential Splice Site, Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000077775 | Splice Site | None | 2043 | None | 16 |
ENSDART00000136624 | Essential Splice Site | 315 | 1368 | 8 | 10 |
ENSDART00000148191 | None | None | 646 | None | 6 |
Genomic Location (Zv9):
Chromosome 13 (position 25098892)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 24744552 |
GRCz11 | 13 | 24875002 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACTATTTAAAACAACTTAGACAAGCCCATGTTTGTGTTTGTTTGAAATA[G/A]CAGGCAAGGGACCATCGTGCAGACTATACTGCTTCAACCAGGAATTTGGC
Long Flanking Sequence:
ATGGGTAAGACGATCAAAGACTATTCTGCTGACCGAGTCTAAGATCAGAGCTTGTGCTTTTAATTGAATCCTATTCAATAGACAGATCATGGAGATCACAATGTGCTCGGGTCGCTCATTCCTTCCTCGACTCTGCATTGTTAGCTTCAAGATGACGCTTGCATGAAAAGTGAGCTAAATTTATCCCATCATTTGCCTTTCAAGAGTTCAGGGTGAGTTCACAGAGATAGCTGAAAGCACTTCCAACTGTAACCCAGCTTCCTGAATGACCTAAATCAAAGCCCTGTATTATTAATGCCTCTGAATGTCCCATGAAATGTAATCTTCCACAGCCGCTTAAAAATAAATGTTGCTGAGATCAACGGCTAATCAAGAGACAATCTCTGCACTGCAGGGGTGCTATGAAGGGAAAAGTGGATAACTGAGATATTATTTGTCTGCTTTGCTTCAGACTATTTAAAACAACTTAGACAAGCCCATGTTTGTGTTTGTTTGAAATA[G/A]CAGGCAAGGGACCATCGTGCAGACTATACTGCTTCAACCAGGAATTTGGCTATGGGGATGGGCTACATTGGCACAAGACCTCCGCTAACCAAGTGCAAGAACTTCAGAAGAAGATACTCAGACCCATTGTTTGGAAACAGCACTGGGAAAGACTTCGAAGTGAGTGAAGAAAGCAGCAGTGATGATGATGATGACAACAACGACGATGATGATGACGATGAGGATGGAGAAGACAGCGCAGTTCAGTCCCAGTCTGGGCAGGGGCTTAAGCGAAGGGTAAAGAATTGCTGATTTTGTCCATTCCCTTATTCAGTTCTTTTAGTATTACTGTTGGTCAAATTTATATCCTTAAGCATTTGGGAAGCGTATTTCACTCGATGGAAACAATATTCCAAACTCTCCATCAGTCTGAAAATTCCATCAATCCTTAAGTCCATAATTAAGTAATATTGCTTTCATGATTTGTGTGGGAAATCTTACGTTTGTATCACCAAGTAATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16535
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 |
---|---|---|---|---|---|
ENSDART00000077775 | Nonsense | 1555 | 2043 | 16 | 16 |
ENSDART00000136624 | Nonsense | 880 | 1368 | 10 | 10 |
ENSDART00000148191 | None | None | 646 | None | 6 |
Genomic Location (Zv9):
Chromosome 13 (position 25096407)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 24742067 |
GRCz11 | 13 | 24872517 |
KASP Assay ID:
2260-6421.1 (used for ordering genotyping assays)
KASP Sequence:
TCTGTAAGATCAGTTAACAGTCCAGCCGTGTCTATTTTAGAAAGTGGTTA[C/A]ACACAAATCAGCCCCGATCAGGGCACCKTTTCAGTGCACTCACTTCATAA
Long Flanking Sequence:
AACAATAAACAACCTGAAGAGCAGCCGAGCCCTGGAGAACCACCGTCTCACTGCTCAGAGGAGCTTGCATCAGAAAGTGCTCTTGTGAACTTGGGCATGCAGGATGGTGACACTGTGGACTCAGATCACACTCCAGACTCAGAAACAGAGGAGGAAGATAATCTTGAAAAGCCTGAAGAAAAGCAAATGGGCCCGTTGACCCCGGCAATAAAAGAGGACCATAACATTTGCCCTGAGCTTGACATGGAGACGGCTCAAGCCGTGCAGTCTCTTACTCAAGAGTCCGAGCAGGAGAGGCACTTTCAGGACTGTGCGGAGACTCAGGAAGCCTGCCACAGCCTACAGCGCTATGTTCACGTCGAGCAGAGCCCTCAGATGACTCCTGTGGATGATTGCCAACAGTCAGATCACAGCAGCCCCCTGTCTTCTGTCCACTCTCACCCGAGTCAATCTGTAAGATCAGTTAACAGTCCAGCCGTGTCTATTTTAGAAAGTGGTTA[C/A]ACACAAATCAGCCCCGATCAGGGCACCGTTTCAGTGCACTCACTTCATAACAACATGGAAACCAGTCCAATTATGGATGTGCCCTCAGTGTCGGACCACTCTCAGCAGGTGGTGGATAGTGGCTTCAGTGACCTGGGTAGCATTGAGAGCACCACTGAGAATTACGAGAATCCCAGCAGTTATGATTCCACACTGGGTAACAGCATTTGTGGCACAGGAGCAGGAGCGGGCGCCTCCTCCCAGAGCAGCTGTTCCTATGGCAACCTCTCCTCCGGTGGCAGCCACAGTCAGAGCAGCTGTGCTGTGTCCCAGCAGATGGCCGGTCCTGTGGTGAACAATACTGGCGCTTGCAGCATGCTCCAGCAAACCAGCATGAGCTCCCCTCAGGGATGCAGTGTGAAGTCTCCGCAAGGCTGTGTGCCCGAGAGGCAGCCTAGCCATTCACATGGACATGGGCATGGTCATGGTCATGGGCATGGGCATAGCCACAGTCACCACCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15696
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 |
---|---|---|---|---|---|
ENSDART00000077775 | Nonsense | 1829 | 2043 | 16 | 16 |
ENSDART00000136624 | Nonsense | 1154 | 1368 | 10 | 10 |
ENSDART00000148191 | None | None | 646 | None | 6 |
Genomic Location (Zv9):
Chromosome 13 (position 25095586)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 24741246 |
GRCz11 | 13 | 24871696 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCTGCCTCACACTCCATCCCATCCTATGCAAACAACAAYGGCTCATTGT[C/A]AACGCAGCTTGGTCCTCATAATCCCACGCTGGTGTMGCTGTCACAGCCCG
Long Flanking Sequence:
CGGTCCTGTGGTGAACAATACTGGCGCTTGCAGCATGCTCCAGCAAACCAGCATGAGCTCCCCTCAGGGATGCAGTGTGAAGTCTCCGCAAGGCTGTGTGCCCGAGAGGCAGCCTAGCCATTCACATGGACATGGGCATGGTCATGGTCATGGGCATGGGCATAGCCACAGTCACCACCACAGCCATCACCAGCACCATCCGCATCATCAACATCACCAACACCCGCAACACCAGTACCAGCAGCCCCTGTCGCACTGCTCCATGCCGGCCAGCTTTCCTCCTCCACCCATGCAGCTGCCCGATATCCCCGAATCCAACAATCCTTCCACTAACCTGGGTCTGTATGACCGAATGGGCCAGGGTGAGTATGGAACTGGACACTATGGTCATCTACATAAGCTACAGCAGCTCACCAACACCATCATGGACCACTCCTTGCCCTTCAGCCATTCTGCCTCACACTCCATCCCATCCTATGCAAACAACAACGGCTCATTGT[C/A]AACGCAGCTTGGTCCTCATAATCCCACGCTGGTGTCGCTGTCACAGCCCGGTGGAGGTCCTCAGTCGCAATCTACTGTGACCCCTCCGCCCAACATGACTCCACCACCCATGATGCTGCAGCGCAACATGGCTACACCAAACATGAACCTCGCCCCCTCGCAGAGACTTCAAACACAAATGCCCCCCAAGAATCACCATCACCACCCCGTGTCCATCCGCTCCAAATCAGCCCCTCTGCCGCCCCACCACCAGCAGCAGATGTATGGTAGGGGTCCTCAGTCCGTAGCCATGCAGGCTCCTGGCAGGACACTGGCAATGCCGACGCGGATGAACATGGGGGTGAACCTCATGCCTGCTCCGGCTTACAACGTCAACTCCATGAACGTGAACGTCAATATGGCGATGAACACCTACAGAGTGACACAGCCCATGATGAACGGGGGCTACCATGGCAATCCTACCTATATGAATCAATCTCCACAGTACTCTATGCAGATGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1676
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 |
---|---|---|---|---|---|
ENSDART00000077775 | Nonsense | 1841 | 2043 | 16 | 16 |
ENSDART00000136624 | Nonsense | 1166 | 1368 | 10 | 10 |
ENSDART00000148191 | None | None | 646 | None | 6 |
Genomic Location (Zv9):
Chromosome 13 (position 25095550)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 24741210 |
GRCz11 | 13 | 24871660 |
KASP Assay ID:
554-1622.1 (used for ordering genotyping assays)
KASP Sequence:
CAACGGCTCATTGTCAACGCAGCTTGGTCCTCATAATCCCACGCTGGTGT[C/A]GCTGTCACAGCCCGGTGGAGGTCCTCAGTCGCAATCTACTGTGACCCCTC
Long Flanking Sequence:
GCTCCAGCAAACCAGCATGAGCTCCCCTCAGGGATGCAGTGTGAAGTCTCCGCAAGGCTGTGTGCCCGAGAGGCAGCCTAGCCATTCACATGGACATGGGCATGGTCATGGTCATGGGCATGGGCATAGCCACAGTCACCACCACAGCCATCACCAGCACCATCCGCATCATCAACATCACCAACACCCGCAACACCAGTACCAGCAGCCCCTGTCGCACTGCTCCATGCCGGCCAGCTTTCCTCCTCCACCCATGCAGCTGCCCGATATCCCCGAATCCAACAATCCTTCCACTAACCTGGGTCTGTATGACCGAATGGGCCAGGGTGAGTATGGAACTGGACACTATGGTCATCTACATAAGCTACAGCAGCTCACCAACACCATCATGGACCACTCCTTGCCCTTCAGCCATTCTGCCTCACACTCCATCCCATCCTATGCAAACAACAACGGCTCATTGTCAACGCAGCTTGGTCCTCATAATCCCACGCTGGTGT[C/A]GCTGTCACAGCCCGGTGGAGGTCCTCAGTCGCAATCTACTGTGACCCCTCCGCCCAACATGACTCCACCACCCATGATGCTGCAGCGCAACATGGCTACACCAAACATGAACCTCGCCCCCTCGCAGAGACTTCAAACACAAATGCCCCCCAAGAATCACCATCACCACCCCGTGTCCATCCGCTCCAAATCAGCCCCTCTGCCGCCCCACCACCAGCAGCAGATGTATGGTAGGGGTCCTCAGTCCGTAGCCATGCAGGCTCCTGGCAGGACACTGGCAATGCCGACGCGGATGAACATGGGGGTGAACCTCATGCCTGCTCCGGCTTACAACGTCAACTCCATGAACGTGAACGTCAATATGGCGATGAACACCTACAGAGTGACACAGCCCATGATGAACGGGGGCTACCATGGCAATCCTACCTATATGAATCAATCTCCACAGTACTCTATGCAGATGGGCATGATGGGTACCCAGCCTTACCCGCAGCAGCCCA
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |