ZMP
amotl2a
Ensembl ID:
ZFIN ID:
Description:
angiomotin-like protein 2 [Source:RefSeq peptide;Acc:NP_001073646]
Human Orthologue:
AMOTL2
Human Description:
angiomotin like 2 [Source:HGNC Symbol;Acc:17812]
Mouse Orthologue:
Amotl2
Mouse Description:
angiomotin-like 2 Gene [Source:MGI Symbol;Acc:MGI:1929286]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa18416 | Essential Splice Site | Available for shipment | Available now |
sa20712 | Essential Splice Site | Available for shipment | Available now |
sa20713 | Nonsense | Available for shipment | Available now |
sa18236 | Nonsense | Available for shipment | Available now |
sa16774 | Splice Site, Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa18416
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 |
---|---|---|---|---|---|
ENSDART00000088914 | Essential Splice Site | 306 | 721 | 3 | 11 |
ENSDART00000139367 | None | None | 41 | None | 2 |
ENSDART00000141354 | None | None | 185 | None | 2 |
ENSDART00000143974 | None | None | 131 | None | 2 |
Genomic Location (Zv9):
Chromosome 6 (position 27702120)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 28003331 |
GRCz11 | 6 | 27993892 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGAAAAGAGAAGTGGACAGCTACAGTGAGAAGGCGGCAAGGTTACAGAAG[G/A]TAACAGGATTCTTTGTGTGATTGCAASTTCSTTGCAACCTTCTAGAACTG
Long Flanking Sequence:
CAATATTCCCATGAGCTCATCGCATAGTTATCCCCAACTCTCTAATAACCACTCTGATACAGTTGTGAATGAGCAGTCAGTTCATCAGCCAGACCAACGGGGTCCTCCCCCGGAGTACCCCTTCATGGTCAGATCCCCTGGATATATGCTTAGTCATTCACAGGAACATGGACACTATTATAATGAGCCCCCTCCTGCCTTCCATTCACAGCATTACAGGTAAAATTATATTTTGGTCACATTGTATATACTGTACACTCTATATGAACATCATGGGTGTTCTAATGTTTATTTTTGTCTCTCTCAGGTTATTTCCAACACAGCCACAAGCACCTCGTCACAATGGCCTGCCCACATTGACCCCTGCTGGCCAGGATGTCAATGTTGGAGGATACAGCATCCCAGCGAACAACTTCCAAATGGAGCAGCTTATTAAAGAGAACGAAAGACTGAAAAGAGAAGTGGACAGCTACAGTGAGAAGGCGGCAAGGTTACAGAAG[G/A]TAACAGGATTCTTTGTGTGATTGCAACTTCCTTGCAACCTTCTAGAACTGTGATGTTTTTGGTATGACCTCACATTTTGCCATGGATGCAAAAAGGCAGCTGTGTCCTTTGATTGTGAACTCAGACATGACCTACAAAGAGTGAGAACAAGAAATCATTGTGCGCTGGTGTCTTCTAGCCTCTGCATTCTAAGAAGATTAGCTCTCTTGCCGTGTAGGAATGCATGCAAGGGAGAGGATCACAAGGACTTCAATTTAATTTGAAAAGGACACATTCTTGGTCACTGAGTGAAAATTCCCAGTAACTTATTTAGCATGCGAAACAACACTGAATTTACCCATGCCTAAAATGCCATGCATTTTTCTGTAATGTGATAATGTCATCACTGAAATACCAGAGTGTTATGGCAGAGCAAGGGGGAAAAACAAGCTTATCTTGGTGTTTGTTTTGCTAAAGTTTATTGGGCCTATTGTGTGTCGTTCAGTGGCAAAAGCTAGATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20712
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 |
---|---|---|---|---|---|
ENSDART00000088914 | Essential Splice Site | 306 | 721 | 3 | 11 |
ENSDART00000139367 | None | None | 41 | None | 2 |
ENSDART00000141354 | None | None | 185 | None | 2 |
ENSDART00000143974 | None | None | 131 | None | 2 |
Genomic Location (Zv9):
Chromosome 6 (position 27702121)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 28003332 |
GRCz11 | 6 | 27993893 |
KASP Assay ID:
2259-7601.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAAAGAGAAGTGGACAGCTACAGTGAGAAGGCGGCAAGGTTACAGAAGG[T/C]AACAGGATTCTTTGTGTGATTGCAACTTCCTTGCAACCTTCTAGAACTGT
Long Flanking Sequence:
AATATTCCCATGAGCTCATCGCATAGTTATCCCCAACTCTCTAATAACCACTCTGATACAGTTGTGAATGAGCAGTCAGTTCATCAGCCAGACCAACGGGGTCCTCCCCCGGAGTACCCCTTCATGGTCAGATCCCCTGGATATATGCTTAGTCATTCACAGGAACATGGACACTATTATAATGAGCCCCCTCCTGCCTTCCATTCACAGCATTACAGGTAAAATTATATTTTGGTCACATTGTATATACTGTACACTCTATATGAACATCATGGGTGTTCTAATGTTTATTTTTGTCTCTCTCAGGTTATTTCCAACACAGCCACAAGCACCTCGTCACAATGGCCTGCCCACATTGACCCCTGCTGGCCAGGATGTCAATGTTGGAGGATACAGCATCCCAGCGAACAACTTCCAAATGGAGCAGCTTATTAAAGAGAACGAAAGACTGAAAAGAGAAGTGGACAGCTACAGTGAGAAGGCGGCAAGGTTACAGAAGG[T/C]AACAGGATTCTTTGTGTGATTGCAACTTCCTTGCAACCTTCTAGAACTGTGATGTTTTTGGTATGACCTCACATTTTGCCATGGATGCAAAAAGGCAGCTGTGTCCTTTGATTGTGAACTCAGACATGACCTACAAAGAGTGAGAACAAGAAATCATTGTGCGCTGGTGTCTTCTAGCCTCTGCATTCTAAGAAGATTAGCTCTCTTGCCGTGTAGGAATGCATGCAAGGGAGAGGATCACAAGGACTTCAATTTAATTTGAAAAGGACACATTCTTGGTCACTGAGTGAAAATTCCCAGTAACTTATTTAGCATGCGAAACAACACTGAATTTACCCATGCCTAAAATGCCATGCATTTTTCTGTAATGTGATAATGTCATCACTGAAATACCAGAGTGTTATGGCAGAGCAAGGGGGAAAAACAAGCTTATCTTGGTGTTTGTTTTGCTAAAGTTTATTGGGCCTATTGTGTGTCGTTCAGTGGCAAAAGCTAGATTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20713
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 |
---|---|---|---|---|---|
ENSDART00000088914 | Nonsense | 345 | 721 | 4 | 11 |
ENSDART00000139367 | None | None | 41 | None | 2 |
ENSDART00000141354 | None | None | 185 | None | 2 |
ENSDART00000143974 | None | None | 131 | None | 2 |
Genomic Location (Zv9):
Chromosome 6 (position 27703854)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 28005065 |
GRCz11 | 6 | 27995626 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGAAGCCCTTGAGAAAACCATGAGGAACAAGCTAGAGAGTGAGATCAAG[C/T]GACTTCATGACTTTAACAGAGATCTCAGGGGTAAGATGGTTCGCATAGCT
Long Flanking Sequence:
TGTTGATTCAATTCCCAGTCCCTGAGGAGCTCTGTGAGAGTGATTCACTAGTGGGCAAGCACCACAGAGAGCCCCAGCCAAGCACATTCTTCCCTCCTTCCCTTTTTATCTCAAATTTTTGTTTGTATTTTTTTCCATTCTTGCTCTTGCGGCTCCTTGTTTTATTACGTTTGGGTTTATGAAACACTACTGTGCCAGCCGAAAAAGAAAAAGTGTCTTATACTTGCCCTCATGTTGTTGAAAATCTGTATCCTGTTAGTTCTTCTGCTTGACACTAAAGGATATTCTTAGGAGTATTTCCAACCTCCTGTGAATCTCCTGTTTAAAGAGACCAGAAACTGATGGGTTTAAATTGGATGTTAACATGCCTTTCTTCTCTCTTTCAGCTTGAACAGGAGATTCAGAGGATATCGGAGGCCTATGAGACTCTTATGAAGGGATCTGCAAAGAGAGAAGCCCTTGAGAAAACCATGAGGAACAAGCTAGAGAGTGAGATCAAG[C/T]GACTTCATGACTTTAACAGAGATCTCAGGGGTAAGATGGTTCGCATAGCTGAGTAATTGTCTTATAAATGAGTTGCATGTTTTGGTATGAGGCAATAAATACTAATTGTTGACTCCCTCATTAGACCGCCTGGAAACAGCCAACAAACAGAGAGCAGCCATTGAAGTTGAAGACAAGAGTCGGCATGCCTTCGCCAAACTGGTTGAGCAAAGTAAGAATTCCCCTTTGCTTCTCTATAAATTATCCTTCTCCCAATGTGCGGTCAACCATGAAACAATCCCAGCTGTTCCCACTGCATTCTTTCATGTTTATATTGTTGGCTTAACGATGCATTCCATTAATAATTAATAATGTGTTCATCATTGAAATGTTTCTTGACAGAGTGCTTTGTTGTATTTAGGCAACATAAATAAATAAATGTATTTAAATAGTCTATGTAATGTAGGATCCAGTACCTGGTTAAGCACATTCTATATTCTTCATCTCATATAGTTGCTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18236
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 |
---|---|---|---|---|---|
ENSDART00000088914 | Nonsense | 453 | 721 | 6 | 11 |
ENSDART00000139367 | None | None | 41 | None | 2 |
ENSDART00000141354 | None | None | 185 | None | 2 |
ENSDART00000143974 | None | None | 131 | None | 2 |
Genomic Location (Zv9):
Chromosome 6 (position 27705710)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 28006921 |
GRCz11 | 6 | 27997482 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGAGCTTATGTGGAGAAGGTGGAAAGGATGCAGAGTGCATTGGCRCAAT[T/A]GCAGGCAGCATGTGAGAAGAGGGAAGCWCTGGAGTTACGACTTAGRACCA
Long Flanking Sequence:
GACACAGGGAAACTTGGCCACTCCCCTGCAAACCCAGACAGACGTGTGTAAATCAAGCATGCCTCTTTTGTTCCAGACTCTTGTGGGAAGCTTATCCCTTGAGAATTGGTTAGAATGAGAGAACAGCCCAGAGAATGCTATGGGCACACCCCAGTCCTACTGCATGGTCATTCATTTTGTGGCCTGTGTGAGAAGCATAATGACTGAATAGCATTGAATGTTCTTGTACCTTTACTGTAGTAAGTTGTCATGGTACATGGTTCTCATTTTGTGTGTCTCTTTTTTTTCCATAGATGAGGACCATCTTCGAGAGCGGGAACGTCTGGAAAAAGAGACACAGCATCTAAGGGCCTCAGGAGAAGAATGGAAGAGGCGTCGTGAAGCCTTGGAGCAAGCACTTATCACAGCTCAGACACGAAATAGGCAGCTGGAAGAAGAGTTACGTAGGAAGAGAGCTTATGTGGAGAAGGTGGAAAGGATGCAGAGTGCATTGGCGCAAT[T/A]GCAGGCAGCATGTGAGAAGAGGGAAGCACTGGAGTTACGACTTAGAACCAGACTGGAGCAGGAGCTGAAGAGTTTGAGAGCACAGCAGGTAAAAGAAAAAACAGACAACTTCTGTTCAATAAGAATCAACAATTTGGGATTAAAAAAGTAAACCACTATTTCTCTTTCAGTGGCAGGCCCAAACCCAGCATGCAAGCCCAGGGTCATACTTGGACCTTAATGTATCATCACTACAGCAGCAACTGAGGGAGAGAGAGGAGCAGGTTTTGGCCCTGGAGGCTGACATCACCCGCTGGGAGCAGAAGTATCTTGAGGAGAGCACAATGCGTCAGTTTGCCATGGATGCTGCTGCTACTGCCGCAGCTCAGAGGTGAGTAAAAGCACAAGTGGTAGAGATGCCATAGTCAAAAAATAGTACTCTTTTTAATTTATTGCTCAACTCTTGCAACAACCATAATTCTCTTTCCAGGGATACCACAATCATCAACCATTCACCCCGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16774
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:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000088914 | Splice Site, Nonsense | 482 | 721 | 6 | 11 |
ENSDART00000139367 | None | None | 41 | None | 2 |
ENSDART00000141354 | None | None | 185 | None | 2 |
ENSDART00000143974 | None | None | 131 | None | 2 |
Genomic Location (Zv9):
Chromosome 6 (position 27705796)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 28007007 |
GRCz11 | 6 | 27997568 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TACGACTTAGRACCAGACTGGAGCAGGAGCTGAAGAGTTTGAGAGCACAG[C/T]AGGTAAAAGAAAAAACAGACAACYTCTGTTCAATAAGAATCAACAATTTG
Long Flanking Sequence:
GAAGCTTATCCCTTGAGAATTGGTTAGAATGAGAGAACAGCCCAGAGAATGCTATGGGCACACCCCAGTCCTACTGCATGGTCATTCATTTTGTGGCCTGTGTGAGAAGCATAATGACTGAATAGCATTGAATGTTCTTGTACCTTTACTGTAGTAAGTTGTCATGGTACATGGTTCTCATTTTGTGTGTCTCTTTTTTTTCCATAGATGAGGACCATCTTCGAGAGCGGGAACGTCTGGAAAAAGAGACACAGCATCTAAGGGCCTCAGGAGAAGAATGGAAGAGGCGTCGTGAAGCCTTGGAGCAAGCACTTATCACAGCTCAGACACGAAATAGGCAGCTGGAAGAAGAGTTACGTAGGAAGAGAGCTTATGTGGAGAAGGTGGAAAGGATGCAGAGTGCATTGGCGCAATTGCAGGCAGCATGTGAGAAGAGGGAAGCACTGGAGTTACGACTTAGAACCAGACTGGAGCAGGAGCTGAAGAGTTTGAGAGCACAG[C/T]AGGTAAAAGAAAAAACAGACAACTTCTGTTCAATAAGAATCAACAATTTGGGATTAAAAAAGTAAACCACTATTTCTCTTTCAGTGGCAGGCCCAAACCCAGCATGCAAGCCCAGGGTCATACTTGGACCTTAATGTATCATCACTACAGCAGCAACTGAGGGAGAGAGAGGAGCAGGTTTTGGCCCTGGAGGCTGACATCACCCGCTGGGAGCAGAAGTATCTTGAGGAGAGCACAATGCGTCAGTTTGCCATGGATGCTGCTGCTACTGCCGCAGCTCAGAGGTGAGTAAAAGCACAAGTGGTAGAGATGCCATAGTCAAAAAATAGTACTCTTTTTAATTTATTGCTCAACTCTTGCAACAACCATAATTCTCTTTCCAGGGATACCACAATCATCAACCATTCACCCCGCAATTCACCCAACAGCAGCTTCAATGAGGATTTGCCGTCCCCCAACCACAGGCATCAGGAGATGGAAAACCGGTATGTCCACCATTT
Associated Phenotype:
Not determined