ZMP
ENSDARG00000057681
Ensembl ID:
Human Orthologues:
ZMYM1, ZMYM4, ZMYM6
Human Descriptions:
zinc finger, MYM-type 1 [Source:HGNC Symbol;Acc:26253]
zinc finger, MYM-type 4 [Source:HGNC Symbol;Acc:13055]
zinc finger, MYM-type 6 [Source:HGNC Symbol;Acc:13050]
zinc finger, MYM-type 4 [Source:HGNC Symbol;Acc:13055]
zinc finger, MYM-type 6 [Source:HGNC Symbol;Acc:13050]
Mouse Orthologues:
Zmym1, Zmym4, Zmym6
Mouse Descriptions:
zinc finger, MYM domain containing 1 Gene [Source:MGI Symbol;Acc:MGI:1915560]
zinc finger, MYM-type 4 Gene [Source:MGI Symbol;Acc:MGI:1915035]
zinc finger, MYM-type 6 Gene [Source:MGI Symbol;Acc:MGI:106505]
zinc finger, MYM-type 4 Gene [Source:MGI Symbol;Acc:MGI:1915035]
zinc finger, MYM-type 6 Gene [Source:MGI Symbol;Acc:MGI:106505]
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa36356 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa17599 | Nonsense | Available for shipment | Available now |
sa32136 | Nonsense | Available for shipment | Available now |
sa23021 | Nonsense | Available for shipment | Available now |
sa36355 | Nonsense | Available for shipment | Available now |
sa32135 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa36356
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000080401 | Essential Splice Site | 201 | 1456 | 6 | 28 |
Genomic Location (Zv9):
Chromosome 17 (position 14611839)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 14762667 |
GRCz11 | 17 | 14770600 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTAGCTCTGTTTATTCTGTCAGTGGGAACAGCAGTGATGCAGTTTCTGG[T/C]AGGAGTCTACAGTGTTTTTTATGTTAATGTACAGTGCCCTACGCTAATAT
Long Flanking Sequence:
TTTTGTTGTCCTTTGTCAGATCTTCAAGAAGAAATACAGTCTGAGCTTAGGATCGAGTCATCGCGAAGTGATGCTATTGTAAGTTTCAATGAAGAACCAATATTTCACAATATTGGCTGCTTGTTAAAGATGTTGTCCTTTTTCATAATAATATCTTTTGTTTTTAATTACAGCCAGAGCCGCATTTAGAAACCACAGACAGAGATACAAGTTACTCACCTGTTATAAGAATTAAGGATGAGCCTATTGATGAAGACTATGATAAAGCGTTAATGCCAGAGTCAGACTTGAGCCGAATTAAACAGGAGCTTGACGGGTCTGATAATAATGAGACAGAGGTAAGTTTGGTTTTCGTGTGGAAGTGCTGTTTTTATCTCATGTAAAATGTGTTAAATGTGATAAAAGACGTCTGCCTCATTTCAGGCCTCCTCTGCATCAGATGAACTGAGGATTAGCTCTGTTTATTCTGTCAGTGGGAACAGCAGTGATGCAGTTTCTGG[T/C]AGGAGTCTACAGTGTTTTTTATGTTAATGTACAGTGCCCTACGCTAATATAAGCACCCTTGATAAATATGAGGATATGAGGCTGTAAAAAAAAAAGTCATTATTGTTTAAAGTCTGCGTGAAATTAAAAATAGCGCACATTGTTATTCTTTAGGTGAACAATTATTAAATTTTGACTGCTGTAGTCACAATATTCTTAACCACACCTCCATATTCTTAACCTCTAATGGCGATGATACACAGGGGAACTTTTTGGGCAATTTTGCAAAGCGATATTGCTTGGCTACATTTCTACCAAAAATTGGTAAGAATATTGTATCATTAACTCATTGCCCAAATTAGTTACCGTTTCCCACCTGGTTTCCAATTTATGGCATTATTTCAACAAATATAACAAAGTTGCCCAGAAATATTGCTCAAAAAGTTGCCTTGTGCATAATCAGCTTTAGCGTTAGTTTGTTATGAGGGAATGATGTTTAAAAAAAAAAAGCCCTGACCCTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17599
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 |
---|---|---|---|---|---|
ENSDART00000080401 | Nonsense | 323 | 1456 | 7 | 28 |
Genomic Location (Zv9):
Chromosome 17 (position 14609628)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 14760456 |
GRCz11 | 17 | 14768389 |
KASP Assay ID:
2261-0770.1 (used for ordering genotyping assays)
KASP Sequence:
CAACCAGCTGTTTTGCTCCACCGTGTGTYTAACGAGTTTCAGTTTACCCT[C/A]GGTTCAGTTTACACCCATCATCGCCCCCAAGAAAACCTGCCACCTCTGCC
Long Flanking Sequence:
AAATATATTAACAAAAGACGTTTTTTCAAAACCTTCTCTTATGTAAACCGTGTAGATTGTGACTTTTCGATTAAAAACAATTTCAATGGTGTACAGGATTTGTCTACTATTCTAATGAGTTTGTTTTCACGCAGCATCCGTGGCACCTTCCCAGCAGTCTTCCTTCTCAGTAATCTCCCAGAGCGCTGCATCACTCAGAGGAACCACTATACTCCTGCCAGCCCAAGCCCAAACTCCACTTCAGCTCCAACTGCAGCATAAGGCCCAGATGCATTCTCAAATCCAGGCACAGGCTCGAATGCAGCCACCCATGATGGCCCAGGCCCAGCTGCAGGCTGTTCCTCCTCAGCCGCCCCAGATCCACGCTCCTCCACCCACAGTCAGGATCTGCTGCTCGGGCTGCTCGAAGGTCCTCCAGAAGGGGCAAACGGCGTTCCAGCGAAAAGGCTCCAACCAGCTGTTTTGCTCCACCGTGTGTCTAACGAGTTTCAGTTTACCCT[C/A]GGTTCAGTTTACACCCATCATCGCCCCCAAGAAAACCTGCCACCTCTGCCTTAAGTGAGTTATCATGTAGAATAATTGTTCTGCTTTTGGGTGTATACGTAACCCTTGTGTGATGTTGAGTGGGGCTGTGCGATTTGGGGAAAATATTAAATTGTGATTTTATTTATGTATTTGTTTTTATTTTTTTCACAATTATTGCGATTTCGATTTGATTTGCTATTTTAATTTTGTAGTCAATCTTCAGCTCAATATTGTGTATTGTTGCTTCTTACAGCTAAAATGCAGTGAGTGTTAGTTAAAAAAAGAAACTGAAAAGATATTAACTTAAACATTTATTCAAATTTGTTTTTAAGCATTCAGAAATTAAACACTTGTTTTTCTGTAGAGCAAACCGTAAGCACAAATAACATGACCTAACCTGTCTGTAAACAAGTTCAACTTAAAATAGGGAGATAGTGCAGCTTATTATACAAACAGAAAATAATAATTATTAAAATACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32136
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000080401 | Nonsense | 845 | 1456 | 16 | 28 |
Genomic Location (Zv9):
Chromosome 17 (position 14594889)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 14745717 |
GRCz11 | 17 | 14753650 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTTTTATTGAAGGTACTGTTTCTAACACCACTACAGTTCAAGCTCCGT[T/A]ATCTCTGTCAAAAGACATGCCTGTAATCGGTGGTGTGGTGTCACTGGCCT
Long Flanking Sequence:
GTGTTTAATAGTTCTGGGATAACCAGCTTTTTGTGCAGCTTTTAATTGTGCATTTATAAAACCTTAAATCAAGGCTCTAACTTGACCAGGTTTTTAAACGCAAGCCAGTGTTTTGTTTGTTGATGGAGTAACATGCACAAGCCGTAGAGACTCCATCCTCTTATCTGGAATAAAGGTTGGGACTCGGCTCATTTGCATATAAAGAAACACACAAAAAACATTTTTACTTTCACCCAAAAAGAGGCATTTACAGCATGGTATTATAATCAATGAGGTGTTTTGAGTTAAAACGTCAGACACATTCTAGGATTTCAGACTTTTATTACATCTTGAAAGCATAAAAGGATTTCTTTAACCATATTTTTATTTAGCAAAATGAGTCATGTTTATGAAAATGTTAAATGTGATTATCAAAACTGGTTGTATATAGACACAGACTCACACATGCTGTTTTTTTATTGAAGGTACTGTTTCTAACACCACTACAGTTCAAGCTCCGT[T/A]ATCTCTGTCAAAAGACATGCCTGTAATCGGTGGTGTGGTGTCACTGGCCTCCACATTACCAGGGAATACCGCTCTCACAGGTATTCATTTCTCATGTTTCATTTTTTCGTTATTACAAAATTGTATGTTTTAATTAAATACAATTTCTTTGCAGGAGCTCTGCCTACCTCAAATGCCAGCTCAAAAAATATTGGCGAAGTAAGTACTGATGCACACATACATTGGGTTACAAAATGTTTAACAAAGTATTTAATAGGGCTTTAGAACAGACGTCACTAAACTTTTCAGCTCTTGGCCCCGAAATAGCAATGCAATCACTTGCAACCCCCAAATTCCTCAGTGGTGGTTATAGCTATACAAATGTTGCGCACACAACAATAGACCTATACACACACAAACATATTGGCAACACAAAAAAGTGCAACAGTCTAACAACCATATCATTTTTATAATCATTTATTAATTTGTTTAATTAATATTAACCTTGCCTAAAGAGACTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23021
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000080401 | Nonsense | 904 | 1456 | 18 | 28 |
Genomic Location (Zv9):
Chromosome 17 (position 14592751)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 14743579 |
GRCz11 | 17 | 14751512 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAGCACACAAACGGATGCTGCAGTGGGTGCTATTCCACATCGAAGAATGT[T/A]GAAGAACAAAGCTCTTATGTGCAGACCTATTACGGAAGAGCAGGGTGTCC
Long Flanking Sequence:
CTGTATTTCTAATGGGATCTGTTAATTTGAACGTGCTAATGAGTCCAGGAAAACAAAATACATTTAGCTGCACAATAAGTAATAAAAATAATGTTTCTTGAGTGGCAAATCAACATATTGAACTTTTTAAAACTAAGTTTTGCTATTTTAAGTAATATTTGGAAACATTTTAACTACTTTTGACCTCAACAATAATGTATTAGCATTAAAAGTATTATCTAATTTATGTATTTGTTTGTTTGCGGTTTTTAATTGTATATTTATTATTGCTGTTTTTGCCATGAAAACAGGCCTTGTTGCTGACATGGCATTAAATAAAAACATATGAGTGTGATGATAATGACCTCAACTCTAGTACCTTTTAATATTTTGTAAAAATAAGAACGCCATTAATTACTGTTTTATAATGTTGATTTTAGCCCTCAAACATTATTGCTCTTTCTTACAGGCTAGCACACAAACGGATGCTGCAGTGGGTGCTATTCCACATCGAAGAATGT[T/A]GAAGAACAAAGCTCTTATGTGCAGACCTATTACGGAAGAGCAGGGTGTCCAGTGTCAGCCAGAGCCGCCAGTCCCTCCAAACATGTCTGAAAAAGGTTGGCCTTCTTTCCTTTCTTGACATTGTTATACTGCCATAATACACAATACTTAAATATTGATTTCACACTTTTTTTTTCTGTTCACAGTGATTAATGAAAACGGAGAGATTGTGAGGTATGTGCCTGTGCCGGTGCCTATTCCGATGCCAGTCTACATCCCAGTGCCAATGCATCTGTACACCCAATACACACCCTTCCCAATGGGGTTCCCTCTACCGGTATGAGATCTTTGCAAAGGCTAATTTCTTTTTTCGATTTGATTTGGGCTAAAAACATTTTCTAAATAACTTGACAGTTTTGCTGTTTAATGCACATCCACATGTCTTCATTTGATTTCTGTTTAGTTTGATTTTGACCTGTCGGATTAATGTCCTCTAGAATCACTTTTTACATGGTCGACTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36355
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000080401 | Nonsense | 1296 | 1456 | 26 | 28 |
Genomic Location (Zv9):
Chromosome 17 (position 14575987)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 14726815 |
GRCz11 | 17 | 14734748 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTTGGGAGCTCTGTCTCCTATTGTTCTGCTTAACACGCTGCTGTTTTTC[G/T]GATCCAAACTGCTCAACCTGAAAACGGTTGAAGAGCATCGACGGCTCGCC
Long Flanking Sequence:
CACCATGGCTATACTGTACATTATTTCAGTTAAGTGACAAGACTTTTGTCTCAGCAATGTCAGACCTTACGTAATTAAATAATTGAAAATCAAGGCATGATCATATTCTATTTTGGTAAACAAAGCCTAAGCGTAATCTAGAGCCCTTTGCCTTTTTTGTAAGCCACTTTTGATACCAAATGATCAACTAGAAGTCAAATTATTATTTGTTATTCCTAAAACTTGGATAGGCGACAAGACTTTAGTTAGGTAGTGTATGCCCAATTTGTAATCAAGATAATATAGGCTTGCTAAGTATAAAATACTTTTCACAAACAACAACAGACTCAACAAACCTTTAATGGTAACCTTTCTTGATCTCTTTTGAAGGGTTTGATTGTGTGTGCTGTTGTGTTTGCACAGGATACATGCACTCGCGGGTGGAGGAGGAATACCTCTGGGAGTGTAAGCAGTTGGGAGCTCTGTCTCCTATTGTTCTGCTTAACACGCTGCTGTTTTTC[G/T]GATCCAAACTGCTCAACCTGAAAACGGTTGAAGAGCATCGACGGCTCGCCTTTTCCAATGTCTCCCACTGCTCCAAGACCACCAAAAGTGGCTTGACCTCTTACCTTCGCTTTAGGCTACCTAACAAAGAGGAGGAAAAAGAGAAGAAATGTAAAAATCCACTGACCACATTGTGTTTAAATCTTAACACGGAGCCTCTATTTGTGTGCATGTTTTCATCGTTTTTAATTTGTGTTTTTTTGAACATGAAGCACCAGCTGGGAAGAGGAAGAGAGATGAAGAGAGCGTGGAGGAGGAGTTTTTGGAGATGCCGGAGAATGTGGAAAATCCTTTACGCTGCCCTGTCAGACTCTATGAGTTCTATCTCTCCAAATGGTGAGTTATTTTAAAGCCGTTGAATATTGGAGAATGAAAATAGCCATTTTGTCTTAATCTGTATTCTTTGTAACACATTTTTCAATTTGACATAGTTTGTGAACTAACTCCTGTTATCTGACTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32135
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000080401 | Nonsense | 1393 | 1456 | 28 | 28 |
Genomic Location (Zv9):
Chromosome 17 (position 14573054)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 14723882 |
GRCz11 | 17 | 14731815 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGACACCTTTTATGATGTTCGTTCTCTCTCACAGCTCAAACTCTGTAAAA[C/T]AGCGTCCAGATCTTTTCTACCTGCAGCCTGAAGCATCCTGCCATCCCAGC
Long Flanking Sequence:
CTAGGATATTAATAACTACTATGTACTGTATGTGTAGTATGCAGGTAATAAAAAAAATATTAATCACATAATATGCTTATTGTAACTCAGGATGGAATCATAAGAAACAAAGCGCTAAATTAACAGCAGTTTTGATCATATAAAGCTTTTGTATGGATTTAGATACTCAGAATATAATGGCTTTGTGTATTAAAAAGAGCAGCTTGGATTTCTGCCTCATTTCTGTTTCACAAAAGAATTCAAATAGCATCACGAATTTGAGTGAATTATACCTGTCATGCATTTTAATATCACACTCAACAATTTTAGAGAGCATGATTTTGAAACTGCATTTGAATTACAGTAATACAGATATTTAAATCCTGCATCATAAGGCTTTTTTTTTCACAAATTGCACTTGCTTAGAGAAGCAGAATCACTTCAAGTCTTTTTCTGGTGCTTTTAGTGAAGCGACACCTTTTATGATGTTCGTTCTCTCTCACAGCTCAAACTCTGTAAAA[C/T]AGCGTCCAGATCTTTTCTACCTGCAGCCTGAAGCATCCTGCCATCCCAGCAGCCCTGTGTGGTACTCAGCCCAGCCACTGGACAGCACCATGATGGAAAGCATGCTAACACGTATCCTAGCTATACAGGACATTCACCTGGACTCGAAACATCAGCAAAAATACCTGGACTCGTCAGACGAAGAGAGCTCTTAATGTGAATCTATAAACTAGACATTCAATGACATCTACTTATTATTTTTATTCAGACCGGGAATGGGATGCAAACAGAAGCGTATGAAATTGTGCACAAGCTCAACAGACATTCCTTAAGCCCATCTATCCTATCATGAATGTTACAGACAGTTCAAATGAACATTTTTGGAGGGAATCGTTTGGTTTTTAGTCACAGTAGACATTGTTTCTCAGTATTTAGTATTATTTAGTGAACGCATTTTAAGTTGAAACATTCATCATGTCATTGTTGGTAACCTTTCAAAAATATATATATGAATTCTCAGA
Associated Phenotype:
Not determined