ZMP
zgc:63660
Ensembl ID:
ZFIN ID:
Description:
zinc finger MYND domain-containing protein 10 [Source:RefSeq peptide;Acc:NP_956691]
Human Orthologue:
ZMYND10
Human Description:
zinc finger, MYND-type containing 10 [Source:HGNC Symbol;Acc:19412]
Mouse Orthologue:
Zmynd10
Mouse Description:
zinc finger, MYND domain containing 10 Gene [Source:MGI Symbol;Acc:MGI:2387863]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa31203 | Essential Splice Site | Available for shipment | Available now |
| sa38262 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa6582 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa31203
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000017413 | Essential Splice Site | 29 | 448 | 2 | 12 |
Genomic Location (Zv9):
Chromosome 1 (position 21465671)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 22000838 |
| GRCz11 | 1 | 22691577 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATAGCCAATGTTGTGTGTGTGTGTTTATTTATTTATTTATTTTTGTAAA[G/A]ATGGTTTCGCCAGCATGAATTTATTGAGAAGCTGAATATGCAAGCTATTC
Long Flanking Sequence:
TACTAATTTGATAACAAATGACAATATGTGAAGCGTCAGAAAGCAAGAAAATAAACAACTTAGCTTTAGGAGGACATTTTTACAGCTTTCTTGTTAGAAGAATAATCTTTTAAGGGGGATCAAATTTTCCCCCACTCCGTCACTTCCGCACTCAGTGTACCTGTAACCATAGTGACGAAACGGAAGATGATATCCCCTAATAGAAGTATAATAGAGTGTGTTTGAAAAGCTGCTAGTTTAGGTTTCTGTAGAAAACATTCTGAAGCGATGGATTCAGTACTTCTACACGAAGAAGCTGAAGGATACATTCAAAGCCTGGAAAAGATGTCATTGCGCGATATCGGAAGCCCGAGGTAAATTACGAGAATATAACATTATAAGTCAAGGATCGGTAAAATAAGAACACGTAATCTAATCCAAAACTAGTATAGCCATGCCATCGTTGTCATGCATAGCCAATGTTGTGTGTGTGTGTTTATTTATTTATTTATTTTTGTAAA[G/A]ATGGTTTCGCCAGCATGAATTTATTGAGAAGCTGAATATGCAAGCTATTCTGAACGCCAGCGCCAATCAGGAGGAATTCATTAAAGACCTTTTCGTTTCTCTCGGAAAGGTAAATTAAATATGATTTTGTTTTGTCGGTCAGTTTCTATACAGGGAATATCATGATATTTTCATGATAGCAGTAATTGTATGTAAACTTTAATGGGATTATAATGTTGTTACTCACTTGATAGAGAGAAATTGTACTCAGGTATAACGTTACTAATATTTATGACCAAAATGTATTGTGGAGAAAAAAAATATGCTTGCCTTGTTCATACTTTTAATACAAGTCCTGCAAACAAAGGTTAGATTTATCTTATGGTTAAAATATTGTACATTATTAATTAATTAATTAATTAATTTATTTATTTATTTATTAAAAACTAAGAGACCACAATCCAGTTTTTCTGGATTTATTATCGGTTTGAGTTAGATTTTATTATTTGATGTAGTTTATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38262
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:
A > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000017413 | Nonsense | 257 | 448 | 8 | 12 |
Genomic Location (Zv9):
Chromosome 1 (position 21470677)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 22005844 |
| GRCz11 | 1 | 22696583 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGAGGGCAAATGGAGAGCCGTCCTCCCTGAAGATCAGCTGAAGCTGAGT[A/T]AACATGATGGCCAGGTGTGGATAGCTTTACTAAACCTGATGCTCAAACCA
Long Flanking Sequence:
CTACTTAAAGGCCTATGAAAGGTTTGAAATGTGCATTTTTATATTTAATGTTTGACAGTATTAACTAAAACATGAATACAGGGTGGGACATAGAGTAGCTCCTCCCCTTTTAAATCAGCTCTGCCAGTGAGAGTGGTTGAGCTTAAGTGCATCAAATGAAAAGCAGTCACAAACTTCAAACTTTGGATGTTTAAATCTTCTAAATGTCTTTGTCACTGTTTTGGAGCACACAAGCTTGACTAAAACTGACATACTCATACTAATACTTGTACTTTTTTAACATCTAAAAAATTATTTTAATTTCACAGGCACTTTAAATCCATAACACTTTCATAGACCTACATTAGAAAAGAGCAAAAGCTTATAATATGATGCACAGCAACAGTTGCTAAGGTAGGATTGACTGCTGGAAGTCTTTTTTTCTCTACATAGGTACACAGGAGAAATACACAGAGGGCAAATGGAGAGCCGTCCTCCCTGAAGATCAGCTGAAGCTGAGT[A/T]AACATGATGGCCAGGTGTGGATAGCTTTACTAAACCTGATGCTCAAACCAGACTGCCAGCGGAAATATGATTTCAACAGCTTCAATAAAACACAACTCTTAAAAGTAAGACTTTAAATATTTGCTTTTCAATAAGGGTTCCTGTAGTGTATCAAGTTGGTATATAAAACTTACATTTTGATTTTGATTCAGACATTAAATATCTGAAGAGGGGATAAATCTGCATTATTCAACGCTGAGTTTGATTTACTCATAACCTAAACATACAGTCTGTTCCTCTAATTCTGATTTATTCAATGTCAAAGATAATTACTGTATGATTTTTTTCTCTGTCTGCATGCAGCTTCGTGGGTTTCTGACAGATGTTGTGATAGATCAGTTACCAAACTTACTTGATCTCAAGCATTTCCTCAGTCAACTTGCTCTCACAGATCCAGTGGCTCCTAAAAAAGATCTCATCTTGGAGCAGGTATTCTACAAACACATATATGTACACTTGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6582
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000017413 | Nonsense | 263 | 448 | 8 | 12 |
Genomic Location (Zv9):
Chromosome 1 (position 21470697)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 22005864 |
| GRCz11 | 1 | 22696603 |
KASP Assay ID:
554-4052.1 (used for ordering genotyping assays)
KASP Sequence:
GTCCTCCCTGAAGATCAGCTGAAGCTGAGTAAACATGATGGCCAGGTGTG[G/A]ATAGCYTTACTAAACCTGATGCTCAAACCAGACTGCCAGCGGAAATATGA
Long Flanking Sequence:
GGTTTGAAATGTGCATTTTTATATTTAATGTTTGACAGTATTAACTAAAACATGAATACAGGGTGGGACATAGAGTAGCTCCTCCCCTTTTAAATCAGCTCTGCCAGTGAGAGTGGTTGAGCTTAAGTGCATCAAATGAAAAGCAGTCACAAACTTCAAACTTTGGATGTTTAAATCTTCTAAATGTCTTTGTCACTGTTTTGGAGCACACAAGCTTGACTAAAACTGACATACTCATACTAATACTTGTACTTTTTTAACATCTAAAAAATTATTTTAATTTCACAGGCACTTTAAATCCATAACACTTTCATAGACCTACATTAGAAAAGAGCAAAAGCTTATAATATGATGCACAGCAACAGTTGCTAAGGTAGGATTGACTGCTGGAAGTCTTTTTTTCTCTACATAGGTACACAGGAGAAATACACAGAGGGCAAATGGAGAGCCGTCCTCCCTGAAGATCAGCTGAAGCTGAGTAAACATGATGGCCAGGTGTG[G/A]ATAGCTTTACTAAACCTGATGCTCAAACCAGACTGCCAGCGGAAATATGATTTCAACAGCTTCAATAAAACACAACTCTTAAAAGTAAGACTTTAAATATTTGCTTTTCAATAAGGGTTCCTGTAGTGTATCAAGTTGGTATATAAAACTTACATTTTGATTTTGATTCAGACATTAAATATCTGAAGAGGGGATAAATCTGCATTATTCAACGCTGAGTTTGATTTACTCATAACCTAAACATACAGTCTGTTCCTCTAATTCTGATTTATTCAATGTCAAAGATAATTACTGTATGATTTTTTTCTCTGTCTGCATGCAGCTTCGTGGGTTTCTGACAGATGTTGTGATAGATCAGTTACCAAACTTACTTGATCTCAAGCATTTCCTCAGTCAACTTGCTCTCACAGATCCAGTGGCTCCTAAAAAAGATCTCATCTTGGAGCAGGTATTCTACAAACACATATATGTACACTTGGGATTAGTAAATTTTCATAGGC
Associated Phenotype:
Not determined