ZMP
si:rp71-69p9.2
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to human ankyrin repeat and MYND domain containing 1 (ANKMY1) [Source:UniProtK
Human Orthologue:
ANKMY1
Human Description:
ankyrin repeat and MYND domain containing 1 [Source:HGNC Symbol;Acc:20987]
Mouse Orthologue:
Ankmy1
Mouse Description:
ankyrin repeat and MYND domain containing 1 Gene [Source:MGI Symbol;Acc:MGI:3045261]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa29745 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa11746 | Nonsense | Available for shipment | Available now |
sa24118 | Nonsense | Available for shipment | Available now |
sa24117 | Essential Splice Site | Available for shipment | Available now |
sa14629 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa29745
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 |
---|---|---|---|---|---|
ENSDART00000090936 | Nonsense | 70 | 994 | 2 | 16 |
ENSDART00000132334 | Nonsense | 70 | 360 | 2 | 5 |
ENSDART00000141528 | None | None | 445 | None | 10 |
Genomic Location (Zv9):
Chromosome 22 (position 15713324)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 15541333 |
GRCz11 | 22 | 15567716 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCGTCACGGCAAAGGCACATACTCCTGGCCGGATGGATCTAAATACACA[G/T]GAAAGTTTTATCTGAATCGAAAAGAGGGATACGGAGTGCAAGTTTTTTCA
Long Flanking Sequence:
TCTTAATTTGGACTGATTCTGACAGTGAAAACTAAACATTATTTTTACTTGGTCAAATAATTTTTGATATTTGGAATAGAAACAAGACAAAACAAAGTAAGAAAAGCATTTTTTGCATTGTGATTATTCAATTTTTGTGCCAGAATATACTGTTAGACTCCACACAAGTCTACCAAATGGAGCCATTCAAACTTTGTTCTGAAACTGTATTAACTGTATCGCAATGTTTATCGCGGAAAAATAAAATATCGCAATATCAGCTTTTCCCAACATCATTCAGCCCTAATATTTATAATCTAAATCACAACATTATAATTATGATATTATATTTAACATTTGTGATTATTTTGTTGCTATTATTATTTGTAAACATCATAAAGTCTTTGCCAGTTTAATATCAAACAATCGTCATGTTTTATCAGTCCTACAAAGGTTCATTTTTCAAGGATTATCGTCACGGCAAAGGCACATACTCCTGGCCGGATGGATCTAAATACACA[G/T]GAAAGTTTTATCTGAATCGAAAAGAGGGATACGGAGTGCAAGTTTTTTCAGATGGATCAACGTTTCAGGTAAACAACTCCCATTTTATTCATTAACAATACATTTGTTTCATAATACATAAAACAAAACCTTTTCTCTTTAGGGCCTATATCATGCAGGTGAACGTTTCGGCCCTGGGGTCATGACATACCCGGACGGCCGACAGGATTTAGGCCTGTGGCACAGAGAAAAGTTACTGCAAATGTGCAGCACAATGGAGGACGGTTTCAGTCTGGAGCATTTCCCAGAATACATGACTAGACGGCTTGAGAAAGACCTGAAACAGCCCCTTTTTCCTGTCGATGTGGAGTCAAGGGCAGACAGAGGTCATTATGTGTCAGATCTGTGTTTATTGGAGGACGAGGATCACTTTATTCTGCCTCCAGAGATCGAGAGGTACTCCACAGACTCAGACCACCTGCCCATCCCGAGGCGTTTGAGGAGAGAGCTGGACCTGCACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11746
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 |
---|---|---|---|---|---|
ENSDART00000090936 | Nonsense | 707 | 994 | 10 | 16 |
ENSDART00000132334 | None | None | 360 | None | 5 |
ENSDART00000141528 | Nonsense | 158 | 445 | 4 | 10 |
Genomic Location (Zv9):
Chromosome 22 (position 15705982)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 15533991 |
GRCz11 | 22 | 15560374 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGCTAGAGATGTGGTGGCGCTTCTCCTTTCTCACTGTGCGAGCCCCAAT[G/T]AAGTCTGGAGTGGYCATTCACCTTTGTCTCTGGCCATCGCCAGTGGCAAC
Long Flanking Sequence:
TAGGCATGCTCAATATATCGTTTACTGTATGTGTTTGTCTTTTGTTTTTGCTATTATGCAGAAAAATGAGAAGGAAATAGGCTAATACATCGTTAATAATACTAAAAGGCTAATATATTGACTATTGGCCCACAAACTAAATATTGGTTATAGATATCGGTTATCAGTATGGGTCAAACACTCCATATTGGTGCATACCTGTACTCACTAGTTATTCCTTTGCGTTTTTTCCTGTTAGTTTGATTTTAAAAATAAGAAAATTAAAAAAACACACCACTAAAGTAACACTGACTTGTCATAGCATTTATATATCACTGCTCTCTAGTGACCTAAAGTGCTTTTATTATTTTCATTTGTGAGTAGTTGTTAGATAATTGACTAAATATAAAATGTAAATGTACAACATTGGTATTGTGTTGTCTAAAAATCAATGCCTATTTGTCTTCCAGAATGCTAGAGATGTGGTGGCGCTTCTCCTTTCTCACTGTGCGAGCCCCAAT[G/T]AAGTCTGGAGTGGCCATTCACCTTTGTCTCTGGCCATCGCCAGTGGCAACCACCTTGTATGTGGTATTTTCTGACATCACTGCATCATCTATTCTGCTGTTATGGGCTCTTTGCACGGAGTGTGTCTAAACCCATTGAAATTCTTCAGATGAAAGGGTTGACGTGATTCTAGTGATCTTACATTTCACTAAAATCCTTGAACAGCATGCAGTTAAAAAAGGATTTCGCTGCTTGTTCAAACTACTTGTGCAAAATGAGCTCAAACAACACAATTTTTGAGATTTTTTTTGGGACAACTTTCATGTTTAAATTGGTTCAGTTTGTTAAGTTAACTCAATCGATTTGTGTTGGGACAACCTGAATGAATTGCATTACAGTGTAATATAATCAGAATCCAGTCAGCAGTCATTAAGTACACACGCATAGTAGTGCCTGTAAATCTTGACCTTGTTGGGTCATAATGTTTAGTCTCCATAAAGAAAAGAGCTCATAAATCATCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24118
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 |
---|---|---|---|---|---|
ENSDART00000090936 | Nonsense | 715 | 994 | 10 | 16 |
ENSDART00000132334 | None | None | 360 | None | 5 |
ENSDART00000141528 | Nonsense | 166 | 445 | 4 | 10 |
Genomic Location (Zv9):
Chromosome 22 (position 15705957)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 15533966 |
GRCz11 | 22 | 15560349 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTTTCTCACTGTGCGAGCCCCAATGAAGTCTGGAGTGGCCATTCACCTT[T/A]GTCTCTGGCCATCGCCAGTGGCAACCACCTTGTATGTGGTATTTTCTGAC
Long Flanking Sequence:
TGTATGTGTTTGTCTTTTGTTTTTGCTATTATGCAGAAAAATGAGAAGGAAATAGGCTAATACATCGTTAATAATACTAAAAGGCTAATATATTGACTATTGGCCCACAAACTAAATATTGGTTATAGATATCGGTTATCAGTATGGGTCAAACACTCCATATTGGTGCATACCTGTACTCACTAGTTATTCCTTTGCGTTTTTTCCTGTTAGTTTGATTTTAAAAATAAGAAAATTAAAAAAACACACCACTAAAGTAACACTGACTTGTCATAGCATTTATATATCACTGCTCTCTAGTGACCTAAAGTGCTTTTATTATTTTCATTTGTGAGTAGTTGTTAGATAATTGACTAAATATAAAATGTAAATGTACAACATTGGTATTGTGTTGTCTAAAAATCAATGCCTATTTGTCTTCCAGAATGCTAGAGATGTGGTGGCGCTTCTCCTTTCTCACTGTGCGAGCCCCAATGAAGTCTGGAGTGGCCATTCACCTT[T/A]GTCTCTGGCCATCGCCAGTGGCAACCACCTTGTATGTGGTATTTTCTGACATCACTGCATCATCTATTCTGCTGTTATGGGCTCTTTGCACGGAGTGTGTCTAAACCCATTGAAATTCTTCAGATGAAAGGGTTGACGTGATTCTAGTGATCTTACATTTCACTAAAATCCTTGAACAGCATGCAGTTAAAAAAGGATTTCGCTGCTTGTTCAAACTACTTGTGCAAAATGAGCTCAAACAACACAATTTTTGAGATTTTTTTTGGGACAACTTTCATGTTTAAATTGGTTCAGTTTGTTAAGTTAACTCAATCGATTTGTGTTGGGACAACCTGAATGAATTGCATTACAGTGTAATATAATCAGAATCCAGTCAGCAGTCATTAAGTACACACGCATAGTAGTGCCTGTAAATCTTGACCTTGTTGGGTCATAATGTTTAGTCTCCATAAAGAAAAGAGCTCATAAATCATCCAGGATGAAGTCATTTGAAAATGCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24117
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 |
---|---|---|---|---|---|
ENSDART00000090936 | Essential Splice Site | 770 | 994 | 12 | 16 |
ENSDART00000132334 | None | None | 360 | None | 5 |
ENSDART00000141528 | Essential Splice Site | 221 | 445 | 6 | 10 |
Genomic Location (Zv9):
Chromosome 22 (position 15703401)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 15531410 |
GRCz11 | 22 | 15557793 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAAAAATAAAGTTCTCATCTCTCTTTGTGTGTGTGTGTGTCTCAATCCA[G/A]CTGGATAAGCTAGTGAAAGCAGGCGCTGACGTTCTCATGCCTGTGATGGT
Long Flanking Sequence:
TCGAGATCTACCTGAGCTTAAACTCCCCTCTCGCCTTGCAAACGGGAAAAAGCCCCGGGCTCGAGGATCTTATTAGCTCAGGGCTCTCCACCGGGACAGCATGTCAAACACGCTTTATAATCAATCATCAGCTAAGTGTGAACTCTTGAAAGTAAATATAATAACATAAAAAATACAGCTGTTATTCCAAATATTCATATGAAGATCGAGTAATTAATGTATTAATAGCTGCAATTTAAATATTGAACATAAAGGATTACTTGGTTTACATTCGTAATGTTTTTTATTTATTCATTATTTTCCAATTTAATTAAATAGAAATAAAAGAACATCACACGTCTGACACAAAAGGCTTGTTTTGTATTTCAATGTTTTTGCAGAAAACATCGAGTCTCACATTCTCACGGTATCAGGCTGAATTATAATAAACCTGCCAATCAAATAAACTGTAAAAAAATAAAGTTCTCATCTCTCTTTGTGTGTGTGTGTGTCTCAATCCA[G/A]CTGGATAAGCTAGTGAAAGCAGGCGCTGACGTTCTCATGCCTGTGATGGTTTGCGATGGCCGCAGGTGTACGATGGGAACAGTAGTGGATTATGCACACATCACATTCCAACAGGTGCAGCTTTTCATCGCCACTTCATTTTAAAGAGCTTCATTTATCGCCTCAGTCATTTACCAGAGGTCTTCTGCTTTCCCTTCAGAACCGGCGCATGTCCCGCACCCCGTATCACGCCCTCAGCAAACACGAAAGGCACGTTTATAATGCCCGCCGGCAGCTGCTCGGACTCATGGGAGATCTGATGAGACAGACCGCCTCCAGGGGGCAAGAGGAACAAGGCCAGGATGAGTTCGGTGAGACTAGACTATTGTTGTTGTTGTTTTTTCATCTCCATTGTTTCGGATTCTGTTTTATCCTCTTAAAAAGATCTAGGTTCTATTATAATAGTACATAAAATACATTTTAGTAATCAAAAAGATGGCTTAGATAATTTAAATCAAGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14629
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000090936 | Essential Splice Site | 807 | 994 | 12 | 16 |
ENSDART00000132334 | None | None | 360 | None | 5 |
ENSDART00000141528 | Essential Splice Site | 258 | 445 | 6 | 10 |
Genomic Location (Zv9):
Chromosome 22 (position 15703285)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 15531294 |
GRCz11 | 22 | 15557677 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGTACGATGGGAACAGTAGTGGATTATGCACACAKCACATTCCAACAGG[T/C]GCAGCTTTTCATCGCCACTTCATTTTAAAGAGCTTCATTTATCGCCTCAG
Long Flanking Sequence:
ATAATCAATCATCAGCTAAGTGTGAACTCTTGAAAGTAAATATAATAACATAAAAAATACAGCTGTTATTCCAAATATTCATATGAAGATCGAGTAATTAATGTATTAATAGCTGCAATTTAAATATTGAACATAAAGGATTACTTGGTTTACATTCGTAATGTTTTTTATTTATTCATTATTTTCCAATTTAATTAAATAGAAATAAAAGAACATCACACGTCTGACACAAAAGGCTTGTTTTGTATTTCAATGTTTTTGCAGAAAACATCGAGTCTCACATTCTCACGGTATCAGGCTGAATTATAATAAACCTGCCAATCAAATAAACTGTAAAAAAATAAAGTTCTCATCTCTCTTTGTGTGTGTGTGTGTCTCAATCCAGCTGGATAAGCTAGTGAAAGCAGGCGCTGACGTTCTCATGCCTGTGATGGTTTGCGATGGCCGCAGGTGTACGATGGGAACAGTAGTGGATTATGCACACATCACATTCCAACAGG[T/C]GCAGCTTTTCATCGCCACTTCATTTTAAAGAGCTTCATTTATCGCCTCAGTCATTTACCAGAGGTCTTCTGCTTTCCCTTCAGAACCGGCGCATGTCCCGCACCCCGTATCACGCCCTCAGCAAACACGAAAGGCACGTTTATAATGCCCGCCGGCAGCTGCTCGGACTCATGGGAGATCTGATGAGACAGACCGCCTCCAGGGGGCAAGAGGAACAAGGCCAGGATGAGTTCGGTGAGACTAGACTATTGTTGTTGTTGTTTTTTCATCTCCATTGTTTCGGATTCTGTTTTATCCTCTTAAAAAGATCTAGGTTCTATTATAATAGTACATAAAATACATTTTAGTAATCAAAAAGATGGCTTAGATAATTTAAATCAAGAAGCTTAATCGATTTTTACAACATTTATGAAGAACATAACGGTTCAGCTAAGAAAAAAAATTCAGTCTTCCTTTCCTCACCCTCCACTTGATTCAAATCTGAGGAAGATAAAATGAAG
Associated Phenotype:
Not determined