ZMP
mysm1
Ensembl ID:
ZFIN ID:
Description:
Histone H2A deubiquitinase MYSM1 [Source:UniProtKB/Swiss-Prot;Acc:Q5RGA4]
Human Orthologue:
MYSM1
Human Description:
Myb-like, SWIRM and MPN domains 1 [Source:HGNC Symbol;Acc:29401]
Mouse Orthologue:
Mysm1
Mouse Description:
myb-like, SWIRM and MPN domains 1 Gene [Source:MGI Symbol;Acc:MGI:2444584]
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa36979 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa31039 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa36978 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa36977 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa36976 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa36979
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 |
|---|---|---|---|---|---|
| ENSDART00000044655 | Nonsense | 32 | 822 | 2 | 20 |
| ENSDART00000125133 | Nonsense | 32 | 716 | 2 | 20 |
Genomic Location (Zv9):
Chromosome 20 (position 9298696)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 9132965 |
| GRCz11 | 20 | 9120704 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACTGTTTTTACAGTGACCTGAGCAGTGCTGAGATTCTCCAGGATCAGTA[T/A]TTACAGTCCGCATGGAGGACAAACAGCAGTGTACTGGTATACATACATGC
Long Flanking Sequence:
ATTCATTCATTCATTCATTCATTCATTCATTCATTTTCTTGTCGGCTTAGTCCCTTTATTAATCCGGGGTCGCCACAGCGGAATGAACCACCAACTTATCCAGCACATTTTTGCGCAGCGGATGCCCTTCCAGCTGCAACCCATCTCTGGGAAACATTCAGCAACACAAACACACACTTATACACTATGGACATTGAAGCCCACCCACTTCAGCTGTACAGCATGGGGGAAACCATGGCATAACAATAAGAATCTAAACTACTGCCATCTGAGGTGCGGAAGCAATAAATAGCTTGAATAAAAATATTGGAAATGTATTTAGTTAGATTACCGTAGAGTTGATTGTATTGTGTTGTATATTGGCATTATCAATTTTACATGTGTATTATTGTGTGGTATTGTGTTTCGTGATGTTTTATTCTTTTGTAGTCTCAACAGTGTATGTTTGTGTACTGTTTTTACAGTGACCTGAGCAGTGCTGAGATTCTCCAGGATCAGTA[T/A]TTACAGTCCGCATGGAGGACAAACAGCAGTGTACTGGTATACATACATGCAATAATTTCTAAAAAACTTTCTCACCATTTACATACACTCAAGTGGGTCTAAATCTTTTATGAATTTCTTTCTTCTCTTGAACACAAAATATGATATTTTGAAGAATGTGGGAAAGAAGCAGTGATTGGCATCCGTAGTAGAAACAAAATAAAAAATTCAGTGGCTGTTTTCCACCCTAAAATTCTTCAGTATGTCCTTTGTGTTAAAAAAAAAAGGGAAAAAAGCTCAAACAGGTTTGGAACAAGGGGAAGGTTAAAAATGATGGCAACATTTCAGTTTTCTCTTTCTCTTTAATACATAAGAAAGATTTGTCATAACATAAAGGATAATATGAGAGTATGTTTTGACTATTACATACATTGCACATTATTTCAAGTTTAAATTTCACAGTTCACATAGTTGTCTCAAATAATCACAATGAGATGAAAAATCAATAATTGTGACAAGCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31039
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 |
|---|---|---|---|---|---|
| ENSDART00000044655 | Nonsense | 201 | 822 | 7 | 20 |
| ENSDART00000125133 | Nonsense | 201 | 716 | 7 | 20 |
Genomic Location (Zv9):
Chromosome 20 (position 9293254)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 9127523 |
| GRCz11 | 20 | 9115262 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGACGATGAGGATGTCGATATTACAGATGACTTCAGCGACAGCGAGTTA[C/T]AGTCTAAAAAGCAGCCAGAACGCTCCGTTTCTCCAGACTGCAACCACCAC
Long Flanking Sequence:
TGATCTGGTCAGTGTTCATTAAAGTTTGAAGTGTGATATTTCTGTTGCATAAAGCTGTACAGTCAAGCATGAAATGGTCCGTACATATGTTAAATTCTGACTTAAAGTTACTTTTATTTAACCAGGATTTTTTTTTTTTTTGCTAGAAATGGCACATGCTTTTTCCAAAAGATAATTAGATGATGTACAAGAGGCATCATGGTGAAAAAAAATATATATATTTCTCAGCTTTTATTTACATCAAAAACTTTAGATCAGAATTTGCCAGGGGTATGAATAATTTCTGTACTTTGTACTGTATATAAAACCTCGACTCTATATAATTTGTGTTTGACCTTCAGCCCAAAGCAGAACCAGCTGCTGAAGTGACCTCCGCTAATGTGACTTCGGTCTCCTCGATTCAACCTCACGTCTCGGCCTTGACTAATGCTGTGCGCATCGAGAGACTCTCTGACGATGAGGATGTCGATATTACAGATGACTTCAGCGACAGCGAGTTA[C/T]AGTCTAAAAAGCAGCCAGAACGCTCCGTTTCTCCAGACTGCAACCACCACGGAGAACTCAGGCCAAGTTTATCAGATGCACTGTTACACCTTCCATCTGAAAGCACTGCTGCTGATGGACAGGCTGATCCAGATTTCAGTGAAGACACAGAAATCCATCATTCCGAAATTGATTCAGAAGCAGTTGAGGAAAGTGGGAATCCTTTTATTAATTTAGACAGCCCAAGCAAACACAGCCTGACTGGAGAGGAGGAAACAGAATTAGCAGGTACATTGACACATCACCTTGTATTATTTTATTCTTTATTTTATGTATGATTTTTTTATTAGATGTATGAATTTATTAGATTTGTATGACTGTTAAACAAACAGGAACATAAGAGAAAATAACACAACAAATAATATAAAAAAATAAATAACATTACTAAATCTTAATTTAGAAACATATATACTGTGCATCCGGAAAGTATTGATAGCGCTTCACTTTTTCCACATTTTGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36978
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 |
|---|---|---|---|---|---|
| ENSDART00000044655 | Nonsense | 292 | 822 | 8 | 20 |
| ENSDART00000125133 | Nonsense | 292 | 716 | 8 | 20 |
Genomic Location (Zv9):
Chromosome 20 (position 9291325)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 9125594 |
| GRCz11 | 20 | 9113333 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATCAGCATGAGCACAACTAGTTAATGTGATCTTTTACTCCAGATAAGTG[T/A]GAATCAGCTGAATGTCTGGAGGAAGAAGTTGAAGACCAAGAGGAGGATGA
Long Flanking Sequence:
TTGGGTTGATCACCTCCCTGACTAAGGCCCTTCTTCCCCGATCACTTAGCTTAGATAACACATGGTGAACGCACGGAAAATAAAGGCTCTTGCTTTTCCACTCCTTTATTTCAGACACTGTAATCAGCTTCTCTCCCATGGTCTATGACAAAACTTAAAATTCTGTGCGACTGCCAAGCTAAATAACGTATTTCAGATTTGTAAAAATGCAGACAGCGGCTTTTAGTGGATTTGTTTCCCAAATGTGTAGGCTGAGACACGCATTTCCAATGAGTTTGGTCCGAAATGTTTAACACTTGTGGCTTAAACTGAGTGCCATTGTGAACATGATGTAAGATCATGACAAAATTTGAGGGAAGAATCTGAATGAAAACCCAACACAAGTGATCACGAGGTATTTTAAAACACCATTGACAGGTGGAAAGAGCGTTTTTTTTTACTATAGCAATCCATCAGCATGAGCACAACTAGTTAATGTGATCTTTTACTCCAGATAAGTG[T/A]GAATCAGCTGAATGTCTGGAGGAAGAAGTTGAAGACCAAGAGGAGGATGAAGAGGAGGAGCTCAGAGCTCCCGAACAAGAGGTTGAATTGGACTTGAACACAATTACTGAAGAGGAAAAGCAAGCTATCTCAGAATTCTTTGAGGGACGCCCATCCAAAACACCGGAGAGATATCTAAAAATCCGCAACTACATCCTGGACCAGTGGTGAGATTTCAGCTTTAAATGTTTCACGTTCTTCTGCCTGGGTTGTACAAGTATCATTAAGGAGCTACTTTTGTTTGTAATTTGTTTTAGATTTTGCTATTGTACTACATACTAAATATGTCTTTTTTATTATTATTTTGATTGCATACAAAGTTTATTTCTAATAAAAAATAGTTTTAGTTTACTGAATTATTTGAGTTATTTTTAAAGAGAATGAATCAGTAAAAATTCTGAAAGATTAAAAGACTTGGTTAATTAATTTATTTATTTGAAAAGTTCATAGTCACCAAGGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36977
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 |
|---|---|---|---|---|---|
| ENSDART00000044655 | Nonsense | 322 | 822 | 8 | 20 |
| ENSDART00000125133 | Nonsense | 322 | 716 | 8 | 20 |
Genomic Location (Zv9):
Chromosome 20 (position 9291236)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 9125505 |
| GRCz11 | 20 | 9113244 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAGGAGGATGAAGAGGAGGAGCTCAGAGCTCCCGAACAAGAGGTTGAAT[T/A]GGACTTGAACACAATTACTGAAGAGGAAAAGCAAGCTATCTCAGAATTCT
Long Flanking Sequence:
TTGCTTTTCCACTCCTTTATTTCAGACACTGTAATCAGCTTCTCTCCCATGGTCTATGACAAAACTTAAAATTCTGTGCGACTGCCAAGCTAAATAACGTATTTCAGATTTGTAAAAATGCAGACAGCGGCTTTTAGTGGATTTGTTTCCCAAATGTGTAGGCTGAGACACGCATTTCCAATGAGTTTGGTCCGAAATGTTTAACACTTGTGGCTTAAACTGAGTGCCATTGTGAACATGATGTAAGATCATGACAAAATTTGAGGGAAGAATCTGAATGAAAACCCAACACAAGTGATCACGAGGTATTTTAAAACACCATTGACAGGTGGAAAGAGCGTTTTTTTTTACTATAGCAATCCATCAGCATGAGCACAACTAGTTAATGTGATCTTTTACTCCAGATAAGTGTGAATCAGCTGAATGTCTGGAGGAAGAAGTTGAAGACCAAGAGGAGGATGAAGAGGAGGAGCTCAGAGCTCCCGAACAAGAGGTTGAAT[T/A]GGACTTGAACACAATTACTGAAGAGGAAAAGCAAGCTATCTCAGAATTCTTTGAGGGACGCCCATCCAAAACACCGGAGAGATATCTAAAAATCCGCAACTACATCCTGGACCAGTGGTGAGATTTCAGCTTTAAATGTTTCACGTTCTTCTGCCTGGGTTGTACAAGTATCATTAAGGAGCTACTTTTGTTTGTAATTTGTTTTAGATTTTGCTATTGTACTACATACTAAATATGTCTTTTTTATTATTATTTTGATTGCATACAAAGTTTATTTCTAATAAAAAATAGTTTTAGTTTACTGAATTATTTGAGTTATTTTTAAAGAGAATGAATCAGTAAAAATTCTGAAAGATTAAAAGACTTGGTTAATTAATTTATTTATTTGAAAAGTTCATAGTCACCAAGGTTGCATGTAATAAAAAAATATGCTTAAGCTTTTAATAATGTGTGAATACAATATTAATATAATTCTGTAAATATTTTAGACTGTTGTTTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36976
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000044655 | Essential Splice Site | 716 | 822 | None | 20 |
| ENSDART00000125133 | Essential Splice Site | 716 | 716 | None | 20 |
Genomic Location (Zv9):
Chromosome 20 (position 9276916)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 9111185 |
| GRCz11 | 20 | 9098924 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATGGACAGGCTTTTTCGAAGAGATTCTTCACTGACTTGCCTGGAGAAGG[T/A]AAAGTTTCTAATTCATTTTTGACAAACCGGCTAATTAAATTGCTTGAATA
Long Flanking Sequence:
TGTAGTATTGGTAACCTATCAACCAGTCCAAAACCACCTCAAGCGAGCATAAAAAAATTATGATATTTTTATATGAAATTTGACGTTTCCATCTGTCGTTTCTCATATTAACACAGGCTGATGCCAACCTAACTTAACTTCTGTAATAAATATTCAACATCATTGATCAATTACATTTAATAATATATACAGAAATACAAAAAACATTATTTATCATTTTTGTCTCATTTCACATAATTTTACAGTATTATTAATAGAACAAATGTAGCCTTGGTTAGAATGTGTGTTGTGTTTTAAAACCATTTTTAAAAATCTTACCAGCCACATTATAGGATGAGATTTTTTCAATACATGATATTATACATGATAATATAAAATGTCCACCATTTGTCCACAGCTTGCTTACCACTGACGTATGTTCATTATTTTTCATTCTTTCAGGAGTGTACCAATGGACAGGCTTTTTCGAAGAGATTCTTCACTGACTTGCCTGGAGAAGG[T/A]AAAGTTTCTAATTCATTTTTGACAAACCGGCTAATTAAATTGCTTGAATATGAAGAAAGAGTGATATGTAAAAGTTTCAAAGATGTTCTAAAGATGATAGCATGAGACCATGAGCGAAATCCTACAAAAACTGAATACTTATACTAATGGTTTACAGTGAATAATTCAATGAATGCTAAAATAGTTTACATATTTATTTGTTACTTTTTTCTGCAAATTAAAAGGCATTTTCTCTAGCATTGGGAATCGTCAGGTATTTTATTAGCATAAAATATTAACTAAAAATTTATATTTTGAAGTTAGTCAATATGATTCCTTTTTGTGTGTCTCAGTCCACATCACAGTCACATTTTAGGATGCTGTTCAATTTATGATGGTAGTAATATTATTATTGAGTAACACTTTCCATTAGTTAATGTTAATGTACTAACTAACATGAACCAACAGCGAACAACATATTTATAACAGTGTTTATATTTTTGACATGTAGCAAGGCAGAG
Associated Phenotype:
Not determined