ZMP
zmynd11
Ensembl ID:
ZFIN ID:
Description:
zinc finger, MYND domain containing 11 isoform 2 [Source:RefSeq peptide;Acc:NP_001071051]
Human Orthologue:
ZMYND11
Human Description:
zinc finger, MYND domain containing 11 [Source:HGNC Symbol;Acc:16966]
Mouse Orthologue:
Zmynd11
Mouse Description:
zinc finger, MYND domain containing 11 Gene [Source:MGI Symbol;Acc:MGI:1913755]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa44159 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa6776 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa44159
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
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000105768 | Essential Splice Site | 222 | 640 | 8 | 17 |
The following transcripts of ENSDARG00000057249 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 24 (position 28109327)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 24 | 27159914 |
| GRCz11 | 24 | 27239073 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATACAAAAGACTGATCCACACGCCTCTGGATGTGGAAAACATACAAGAG[G/A]TAAAAACGAATTAAAAAATAAAGATCTCCCAGCGGTTTTGGCATGTTCTT
Long Flanking Sequence:
TAACAAACATCCGACCAAATAATGTAGAATAGATTTGTGTCATGCTGACAATGAAAGGTCAAACAACTACTCACCCATATGAAATCCTCAGGAATGTAAATTGAAGTATTTCACAAACATGCTTTTAATTTATTCGTTTGAAACCTTAAACCATTGTGAGAGTAATTTAGTGCAGATGATGTGGTTAATGAGTCATTTGTTTTTTGTGATGATATTTACTAACAGGGCAGTAAAAGGAAGAATTTGAACAAACAGGAAATGACAACATACCTGAAGTTCATTCTTGGACGCATGAAGGAAAGGGTGCGTTTCACACTTTTACGTCACACTTAATCGTCTGCGTATTTTCTGTTAAAATAAAAAAGTGAAACAGATTTAGATGTTGTCTTCTAATCTGATCTTGATAGGCTGTAGACCTGCACAAGAGAGGCAAAGAGGCAAAGCAGCCCATATACAAAAGACTGATCCACACGCCTCTGGATGTGGAAAACATACAAGAG[G/A]TAAAAACGAATTAAAAAATAAAGATCTCCCAGCGGTTTTGGCATGTTCTTATGTTTATTTTCCTCTACAGAACATCTCAGATGGGAAGTACAAGAGCTTTGAGGAGTTCAGGGCTGATGCTCAACTTATAGTTCACAACACCGCCATTCTGCACGGAGGTGAGGTTTAAAACTGGTGTGATTTATAAATAAAACACTGTGGAGCAAGGTGTCAACCGTTTCCTCATTCTCTGTCAACAGTCAACAGCGATCAGACTGAAATTGCGAGACTTCTCTATAACGACACATGCCATGAGGTCAGAAAGAGCAACACTTGTTGAGTGCTTTTCCTTCTAGATTTATGTTAATATATAAATTATATGTTCCAGCTGAATGAGTTAATGCTGTGCAGAACCTGCTTTTATCTCTCAAATGCGCGACCTGACAATTGGTTCTGCTACCCATGTGTAAGCACAGATCCAGACACTTAATTCTTCACGTCTACGCCTGTTGTTTTGCATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6776
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000105768 | Nonsense | 407 | 640 | 13 | 17 |
The following transcripts of ENSDARG00000057249 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 24 (position 28106819)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 24 | 27157406 |
| GRCz11 | 24 | 27236565 |
KASP Assay ID:
554-5020.1 (used for ordering genotyping assays)
KASP Sequence:
ACGACAGGTCAGAGAGGCACGAAAGGCAGGAAGAACGACAGGAAGAAGCY[G/T]AGTCAAGCATCTCGTCCACATCCAATGAGCAGGTGAGCACTTTTCTGYTG
Long Flanking Sequence:
GACAATTTAATTCTTTTTATAATCCAAATATTAATTTTGATGTTTAATGCAAGTTAGAATTGCTTGTTAAGATCTTAAATCTAAAGTTAGATGAATGTTTGAAATGTTACTTAAATATCTGATCATATTTACACAATAGGTGACTACTGTACATATGCTGTTAGAAGTCAAAAGTTTGTGAAGTTATTGTATTGCCCAACGCTACTGAGTTTTGACTCTCCTTAATTGTAGACCTGGACCAAAAGCTTAATGTGAGCACACTAACAAGCTTGTGTCTGTTTTGCTGTAGGGCATGGATTCCTTCTGACAACATCCAGGACATCACGGTCAGTGTGCAGCAGCTGCAGGTAAAGCGCAGCTCAGGCTGGAAAAAGGCCTGCGATGAGCTGGAGCTCCACCAGCGCTTTGTGAGGGAGGGCAGAACCTGGAAGGGCAAACCGGAGGAAAAGAACGACAGGTCAGAGAGGCACGAAAGGCAGGAAGAACGACAGGAAGAAGCC[G/T]AGTCAAGCATCTCGTCCACATCCAATGAGCAGGTGAGCACTTTTCTGCTGCATGGAAAATGTCACTGTTCACCTTTCAAGACTTTATTGAACATCCTTCTGAATTTTGCAACAGTCTAGAGTCAACCAAGAGCCCAAGGCTAAAAAGAGCCGTCGTTCCCAAGTCGCCGAGCCCAAAGAAGAGGTTTGTACCACATAATTATTTTTAAAATATATATGTTGGACCTATTTACTCTGGCTGACGTCATGTGTTTTCTCTGATCAGATAGCGATCTGATTTATGAAAATGGTTCCATTTACATTTGGCTACATACAGTAAATGCGCCTCTGCTAAACGGATACGATTCTGAACCTTAAATCCAGAACCCTAGACAAATTCAATGAGGTGATGTTGACTAAAGCATCAGATACAGCGTGATTTATTTCAATAATATATTAGTTTTTACAGAAACTTACTTTATCTTATTCAGCATACGAATGATTTTATATATTGGCTATAGG
Associated Phenotype:
Not determined