ZMP
si:dkey-13f9.6
Ensembl ID:
ZFIN IDs:
Human Orthologue:
AMOT
Human Description:
angiomotin [Source:HGNC Symbol;Acc:17810]
Mouse Orthologue:
Amot
Mouse Description:
angiomotin Gene [Source:MGI Symbol;Acc:MGI:108440]
Alleles
There are 7 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa1663 | Nonsense | Available for shipment | Available now |
| sa3123 | Nonsense | F2 line generated | Not yet available |
| sa12125 | Essential Splice Site | Available for shipment | Available now |
| sa12810 | Nonsense | Available for shipment | Available now |
| sa16908 | Nonsense | Available for shipment | Available now |
| sa3119 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa1663
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 |
|---|---|---|---|---|---|
| ENSDART00000114778 | Nonsense | 12 | 968 | 1 | 10 |
| ENSDART00000141096 | Nonsense | 12 | 606 | 3 | 7 |
Genomic Location (Zv9):
Chromosome 21 (position 36839933)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 37829282 |
| GRCz11 | 21 | 37514469 |
KASP Assay ID:
554-1610.1 (used for ordering genotyping assays)
KASP Sequence:
GTCACGAGATCTGGAAATGAGGGCAGCAGCCTCAGTTTCCGAGGACACAT[C/A]GGCTAAYAACAGYGGTGGGAGTGGACACACGGTTCTGCAGCGGCTCTTGC
Long Flanking Sequence:
GGGTGAACTTCAACACCTTGACACTGGGCTCAATCTTTACAAAGCTGCAAGATACAACTTTATCAATCCCTAATTAGCAAGTTGATGGGAATTAGTAGTGGTTACAGTTACAATTGTCGCATTTAAAATGTAGATTGGTCATAGATTAGCAAGAGAAGTTACTTATTGTTGATTTTTAAAGAATATGGTGCCCAGCTGTCAATGTGTGAAAAGTTTGGGGCAGTTGGGGTCTGAGATTTCAGACATTTCTCTTAGAACATGCAGAATATTTGTCAATCTCTTTCAGCTTATTTTTATTCAGTTTCTGCTTTTTAAACTTTTTTTGGCAACATCATAGTTCAGCCTATGGTCATGGTTGGTGGCTGAGCGTATCATTGATTGTTCATTGATTGTTCATTACACAGGGAGTGTGGATCGTGCCCGAAGCTCCTCCTTCCATGAGGTGGGTAGGTCACGAGATCTGGAAATGAGGGCAGCAGCCTCAGTTTCCGAGGACACAT[C/A]GGCTAACAACAGCGGTGGGAGTGGACACACGGTTCTGCAGCGGCTCTTGCAGGAACAAATGCGCTATGGCGAGGGTCGAAATTACCTTGCCTTGCAACAACAGCAGCAGCAAGGTCCAGTAAGCGGATACCCAGGGCCTGGCAGCCCAGCAGACGAGCACTCGATGGTCCCACACATTGCGCGACAAGAGCCTCAGGGCCAGGAGTTGCAAGTTGACAGTGGCATGGAGAAGCTCAGCACACGCACTGCAGGAGGAGGCGGTGGTAGCGGAGGCACCGGGTCACTTGGTGGTAGTTGTGTCAGTGGGCAGATGCAGAATCCAGAAGACCTGCCCACTTATGACCAAGCCAAGGTTCAGTCGCAGTACTTCCGTGGCCATCAACCCCAGCAGCCTCAACCACAGATGCCCCCAACAGTGGGTGCTGCTTTTTATGTGACTGGAGTCACCAACTCTAAGGTGCGACCCCCAGAGGGCAGGTCCACGGTGCAGAGAATGAATG
Associated Phenotype:
Normal
| Stage | Entity | Quality | Tag |
|---|---|---|---|
| Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa3123
Status:
F2 line generated
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 |
|---|---|---|---|---|---|
| ENSDART00000114778 | Nonsense | 64 | 968 | 1 | 10 |
| ENSDART00000141096 | Nonsense | 64 | 606 | 3 | 7 |
Genomic Location (Zv9):
Chromosome 21 (position 36840088)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 37829437 |
| GRCz11 | 21 | 37514624 |
KASP Assay ID:
554-2955.1 (used for ordering genotyping assays)
KASP Sequence:
AGCAGCAAGGTCCAGTAAGCGGATACCCAGGGCCTGGCAGCCCAGCAGAC[G/T]AGCACTCGATGGTCCCACACATTGCGCGACAAGAGCCTCAGGGCCAGGAG
Long Flanking Sequence:
AAGTTACTTATTGTTGATTTTTAAAGAATATGGTGCCCAGCTGTCAATGTGTGAAAAGTTTGGGGCAGTTGGGGTCTGAGATTTCAGACATTTCTCTTAGAACATGCAGAATATTTGTCAATCTCTTTCAGCTTATTTTTATTCAGTTTCTGCTTTTTAAACTTTTTTTGGCAACATCATAGTTCAGCCTATGGTCATGGTTGGTGGCTGAGCGTATCATTGATTGTTCATTGATTGTTCATTACACAGGGAGTGTGGATCGTGCCCGAAGCTCCTCCTTCCATGAGGTGGGTAGGTCACGAGATCTGGAAATGAGGGCAGCAGCCTCAGTTTCCGAGGACACATCGGCTAACAACAGCGGTGGGAGTGGACACACGGTTCTGCAGCGGCTCTTGCAGGAACAAATGCGCTATGGCGAGGGTCGAAATTACCTTGCCTTGCAACAACAGCAGCAGCAAGGTCCAGTAAGCGGATACCCAGGGCCTGGCAGCCCAGCAGAC[G/T]AGCACTCGATGGTCCCACACATTGCGCGACAAGAGCCTCAGGGCCAGGAGTTGCAAGTTGACAGTGGCATGGAGAAGCTCAGCACACGCACTGCAGGAGGAGGCGGTGGTAGCGGAGGCACCGGGTCACTTGGTGGTAGTTGTGTCAGTGGGCAGATGCAGAATCCAGAAGACCTGCCCACTTATGACCAAGCCAAGGTTCAGTCGCAGTACTTCCGTGGCCATCAACCCCAGCAGCCTCAACCACAGATGCCCCCAACAGTGGGTGCTGCTTTTTATGTGACTGGAGTCACCAACTCTAAGGTGCGACCCCCAGAGGGCAGGTCCACGGTGCAGAGAATGAATGGAGGCAAAGTACACCAAGATGATGGGCTCAAGGATCTAAAGCAAGGTCATGTACGTTCTCTCAGCGAAAGACTAATGCAGCTCTCATTGGCCACCAGCGGGGTCAAGGCCCATGCTCCTGTTACCAGTTCACCACTTTCCCCCCAGCTGCCTCCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12125
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000114778 | Essential Splice Site | 479 | 968 | 3 | 10 |
| ENSDART00000141096 | Essential Splice Site | 479 | 606 | 5 | 7 |
Genomic Location (Zv9):
Chromosome 21 (position 36842473)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 37831822 |
| GRCz11 | 21 | 37517009 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAATCTGTTTTGTTGTTTCTGTGAGGCCTCAGCAATGTAAWCTCTTTACA[G/T]ATGGAGACTGAGATCCAGATGGTGTCAGAAGCTTACGAGAACTTGGCTAA
Long Flanking Sequence:
TGCTCAATTTAGGTCATAACCTGTACCACATCCACTTAAATGAAACCATTTCCATGTCAGTGCAAATGTAGGTCAGTTCAGGATAGGTCAGTGTTTTCAACTTTGTTCTTGGAGGCACAGCAACAGAAAACATTTTGGATGTGTTGGGTATCTGATTATTCTGTTTCTGGAGTCCTGTAGATTCTACTTACAAGCTGATGAGTTGAATCAGGTGTGTTTAATAACAAAGATGTTTAAAAGTGTTTGGTGTTTCTATGGAAAAAAGAGTTTATAAATATTATAATAAGCTCTCAGATGACCAAGGATCAACTCTGGCATGATAACCATCTAAACTTTTGATTCAACAAGCTTTGAAAAGATTTTTAGGTGACACATCAAGAGTGACATCAACATCAAGAGTGACACATCAAAAGTGGAAGGCAATGTTGCATGCTATGTTTTAGTTGTACAAAATCTGTTTTGTTGTTTCTGTGAGGCCTCAGCAATGTAATCTCTTTACA[G/T]ATGGAGACTGAGATCCAGATGGTGTCAGAAGCTTACGAGAACTTGGCTAAATCATCCACAAAGAGGGAAGCTCTTGAGAAGACCATGAGAAATAAGCTGGAGATGGAGGTGCGCAGGGTGCACGACTTCAACAGGGACCTACGAGGTGAGAAACATAGCAATATATCGGAGTATTCTGAAAGTATTAGGAGGAGATTATTATGAAAGGAAGATTCATGAATTGTACTTTACCACTATACTACACCTTTTAGCAGTAAAATTGTCACTGATCTCAAAACATGTTTGTGTTGTTCTTGGCTTAAATTGCTCTACCAATTGTGGTTTTTATCCCCTGAGACCTTTTCTTGTAACATAAATATGAGATCTCAGTGACCCTTCATAGACAGTAATGGCCCAGAGACATTCAAAGCCCAGAAAATTCACCGGAAACATTGCCAAAACATTCAGAGTGACATTCTCAGTGGTTTAACTGTAATCATACAAGGACACTTGTATAAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12810
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 |
|---|---|---|---|---|---|
| ENSDART00000114778 | Nonsense | 553 | 968 | 4 | 10 |
| ENSDART00000141096 | Nonsense | 553 | 606 | 6 | 7 |
Genomic Location (Zv9):
Chromosome 21 (position 36852026)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 37841375 |
| GRCz11 | 21 | 37526562 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCGCTGCAAAAGAGTGTGAGGGCACAGAGGAYAATCGWAAAACCATCTCA[C/T]AGCTTCWGGWTCAGGGTGAGTGGACCTACAGGTACAAGAAACCCGGAAGT
Long Flanking Sequence:
AAACAAAGTATTGATCAGGTTGATATTATATAGGTCTTAGAAACTCGTGTATCAAATATGATACGTGCGGCTTTAATATGGAAATGTATGCATTTTCATTGGAGTTTATGTACTTGTCTGCTGCTCTTGATACCGTTTGCTTTTAAACTTGCATCTTTTACCTTGCTCTATGTTTAAACAATTAAATGAATGCTTAAGTCTATTCAACGGATTATATTTTAAATAAATTACATTATCGGTGCTGTAAAAGGAACCTTATTAAATTGAAAATAGTTACATTAACCTTTCTCCCAAAGTTAATTAAAAATTTTTATAAAAAAAAAAAACACTTGCTGTTGCTGTGCATATATCATTGTGCATATGGAATTTTTAACCATAAATTAGACAAATTTGTGATTTAGATTTGTCTCCTTCTCTCAACAGAACGAATGGAAACGGCCAACAAGCAGCTCGCTGCAAAAGAGTGTGAGGGCACAGAGGACAATCGTAAAACCATCTCA[C/T]AGCTTCTGGTTCAGGGTGAGTGGACCTACAGGTACAAGAAACCCGGAAGTTCCTTAAAGGCAATATAATGAGCTTAAATTAAATGTAGGTTTGTTTTGAATTACCATTGATTTGTGAACACAGATGGTAGTTGCAATAAATTGGGAGGGAAAGTGCAAAATGTTCATTTTGCTCTTTTAACAGTTAAAGAAAATCAACGAGAAAAGGAGAAGCTGGAAATCGAGTTGAATTCACTTCGTTCCACAACAGAGGACCAGCGCAGGCACATCGAGATCCGTGACCAGGCCTTAAACAACGCGCAAGCCAAAGTGGTCAAACTGGAGGAAGAGGTAAAATGTTTTACAATTTGTCAATTTACTTTTTTGAATTTTGAATTGGAACAACTTTAGTGTTCACTTTATTGGGTAACACTTTACAATAAGGTTCATTCGTTAATGCATTTACTAAAATTAACTAATCATGAACAACACATGTACAGCATTTATTAATCATAATTGAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16908
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 |
|---|---|---|---|---|---|
| ENSDART00000114778 | Nonsense | 719 | 968 | 7 | 10 |
| ENSDART00000141096 | None | None | 606 | None | 7 |
Genomic Location (Zv9):
Chromosome 21 (position 36861016)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 37850200 |
| GRCz11 | 21 | 37535387 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGAGCGTCATGAGGCAGTTCGCACTGGATGCCGCTGCTTCTGTGGCCACA[C/T]AGAGGTGRACACATWCACTGCTCTACACTGAACATGCRCTGTACAATTAG
Long Flanking Sequence:
NNNATATATATAATTTGTACTTTAATCCATTTTATTCTAAGTGCTTGTAAAATGTTTGTCCCAAAAGTATTTGAAGAAAACGGTCAGCTTTTTTTTCTGTGGTGATTTGCATTGTGCGCTCTTGAGCTTGTCCGAAAACATCAACACAACGCGACTCACCCTGACGTAGATTCCCATTCTCTATTGGCCTCTTTACAGCTGTTCAATTCATGTGTTTCTTCTGTTCACATAGCTATCTGATACGTTTGGCCACATAAATACATCTCTAATATACGGATATGATTCTGCTCTTCTGATTTCTCTCTCAATCCCAGAGACAAGGTGGCTCTCAGAGCACGGTTGGCCCGGAGTTCAGCACAGCGGCTCTGATGGAGCACCTAAGAGAAAAAGAGGAGAGGATTTTGGCCCTAGAGGCCGACATGACCAAATGGGAGCAGAAATATCTGGAGGAGAGCGTCATGAGGCAGTTCGCACTGGATGCCGCTGCTTCTGTGGCCACA[C/T]AGAGGTGGACACATACACTGCTCTACACTGAACATGCACTGTACAATTAGTTAGTAATTAGTTCTCAAAGTTAAAAATGACCATTGAAAAAAATGTTTGACATAAAACAATGCAAGTTTGCGAAGCATCAGTGTTAAACATCAACTGTAAAGTGCGCTACAGTGCCAATGTGGCAGTTTTTTTATTTAAAGCGACTCTCTATGATATGAAATTAAACTAAAACCCTATTTTTTAAGCCCTTTCACTTCACACTCCAAAGGTAAGGGGTAGGGGTAAAAACATTGAATTGGGCCTAAAAATTGTGATTACTATTGGATAAAAACTAAAACTCTCTGCACCAGTAAATCTAACTTTAAATTAAAGTTTTTTTTTTTTTTTTTAAATCAAGCTATACAGTGCTCAGCATTTATAAGTACACTCATCACAAATCTATCTTTTAAATTCATATTTTTAATAGGAAGCTAAACAATATTATATTTGTGCAAATACATTAGTCAGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa3119
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 |
|---|---|---|---|---|---|
| ENSDART00000114778 | Nonsense | 853 | 968 | 9 | 10 |
| ENSDART00000141096 | None | None | 606 | None | 7 |
Genomic Location (Zv9):
Chromosome 21 (position 36864702)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 37853886 |
| GRCz11 | 21 | 37539073 |
KASP Assay ID:
554-2814.1 (used for ordering genotyping assays)
KASP Sequence:
CCTCAATCTGATTTGCTCCTCTTCATGTTTCAGGTGTTCTGCTGGGTCCA[G/T]AGTTCCGTGGAGACTCTCTGAGAACAGAGTCCATTTCCTCTTCTCCATCT
Long Flanking Sequence:
ATCATTGAGAAGGACGCCATGATCAAGGTCCTCCATCAGCGCTCGCGGAAAGAACCCGCCAGCAAGCTGGACACTCCGGCCATGAGGCCCTCCAAATCCCTAATGTCCATCGCCACGGGCACTGGCGGCTCCAGTGGCTCCGGCCTGCTGTCTCACTCTCTGGGGCTCAGCGGCAGCAGCCCGATCACGGAGGAGCGCAGGGAAGACCGCAGCTGGAAGGGCAGTTTGGGTATGTGATGTACTGTTCAAATGACTTCCCTTTTATTATGTTGGGGGCTGTTTTTTCCCCCCAATGACTTCCATTGTAACCACATTTTTTTTTGCATTCTTGATTGTTTGCAAAAAAGTTTTTGACTTTTATAAGCAATTCTATGGAGTAAAGCAACAAATTATGGATTATATTACCATTTTTACTATGTTCTTAGAGCTGACTTGCAGATTTTTTTTCTTCCTCAATCTGATTTGCTCCTCTTCATGTTTCAGGTGTTCTGCTGGGTCCA[G/T]AGTTCCGTGGAGACTCTCTGAGAACAGAGTCCATTTCCTCTTCTCCATCTCCAGTCCTGCCCTCCACTCCGATGCCCCTAGCCACACACTCAAAGACGGGCAGCAGAGACAGCTGTACGCAGACAGAGAAGAGCCAGGAGAACAGCAAACCCAGCACACCTGCCCTGCAGAACGTCCCAGGACCCAGCCGAATCAGCAGCCCCAGCCCCGTCTACATTCCAGACCGCATCGCCGGTACATATCTCTCTCTCTCACACACGCACACACACATTACACACTATCAATCTGATGTTTGTCATCCAAGTTCTTCTTCACTTTAAGTTTATCTTTGCATTGCAACCTATGACAAGAACCAGCTGCAGAGAAAGTGTTTAAAATATATAGTTAAATAATATTTGTAATAATTAGTTTAGTCTTTTTTTTTTTTTTAAATATGTTGTTTAATTTACGCAACACAAAATGCAATTAAGCATAAGATGCAACTCATGTATGCCTTACCT
Associated Phenotype:
Not determined