ZMP
WAPAL (1 of 2)
Ensembl ID:
Description:
wings apart-like homolog (Drosophila) [Source:HGNC Symbol;Acc:23293]
Human Orthologue:
WAPAL
Human Description:
wings apart-like homolog (Drosophila) [Source:HGNC Symbol;Acc:23293]
Mouse Orthologue:
Wapal
Mouse Description:
wings apart-like homolog (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:2675859]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa19030 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa9959 | Nonsense | Available for shipment | Available now |
sa13582 | Essential Splice Site | Available for shipment | Available now |
sa35225 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa35226 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa19030
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000032195 | Nonsense | 242 | 1168 | 2 | 19 |
ENSDART00000032195 | Nonsense | 242 | 1168 | 2 | 19 |
Genomic Location (Zv9):
Chromosome 12 (position 12785448)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 11641101 |
GRCz11 | 12 | 11679404 |
KASP Assay ID:
2260-5075.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTCATCTTCTATGTTGTGGGCATCCAGTAGTTACAGTCACAGCAACATT[C/T]AGGGCAAATCCTCCACTGAGACTCGGTTAGACAACTTCCACCAAGGGGAA
Long Flanking Sequence:
CTGTTTTTTTTTTTTTTTAATCCACTTCAAATGTTGACTGTTCTAGATAGTTTTAATAACAGTATATATATTTTTAAAGTAATTAGTAGCTACAGATAGATTAATGTTATGTTGAAGATGACAAATTTATCTTTGCAGTTGCTCACTTTAATTTGCCTTCATCAGGCACTTGAAATTGGTTGAGTTCACTTAAATTCTGTCACCTCATCAGACTGATTTTTTTTCTGCTTGCTTTCATTTCTTTAGGAAAGACCCCAAGTTGGCCTGCCGAGAGCACAGATCGCCACAGCTACTCATGGTACAAAAACCCTTCTGAATGTGACACACGACCTCTTGCCCAGACCACAACATTAAAGTCTGAAAAAACAGAGGACAAGGATTCGTATGATGCCTGGAGCGCTGTGGTTGGTCTAGGGGCACGCTCTACATCCCTCTTTACTGCACCTAAAGAGTCATCTTCTATGTTGTGGGCATCCAGTAGTTACAGTCACAGCAACATT[C/T]AGGGCAAATCCTCCACTGAGACTCGGTTAGACAACTTCCACCAAGGGGAATTTAATGTTCCTGTTGAGCCGTCTGAAAGCGAGGACCACTCTCAGTCTGTGCTCAGGGCGCCTAACTGCAGAACGTACTGCAGACCCAATAAAGGCAAACAGCCTGGTGGAGCTGATGGGAGCGGAAGTGCTTCCAGTCATATCTCCACAGGAGTGTTACAGACCATTGGGACTGACAATGCTAGTAAAACAACGAACAGAGGTCGGACGAGAGACTTTACAGTGTTGCACCCATCTTGTGTATCCATGTTTAACGTCACCTTTCAGGACTCTATGGACCGCAGTGTAGAGGAGTACACAGCCAGCACCCAAGCGTCTGGTCCAGGAGATGAAGGAAGACTGAAGAAGAAGACTGAGACGGAAAGCAAACCTTTGAGGTAATAGCTTGCTAAACTAATATTATTCAAATCATATTAAAGGCATTTCACAGCATTATTTTCAGTTGTTATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9959
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 |
---|---|---|---|---|---|
ENSDART00000032195 | Nonsense | 242 | 1168 | 2 | 19 |
ENSDART00000032195 | Nonsense | 242 | 1168 | 2 | 19 |
Genomic Location (Zv9):
Chromosome 12 (position 12785448)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 11641101 |
GRCz11 | 12 | 11679404 |
KASP Assay ID:
2260-5075.1 (used for ordering genotyping assays)
KASP Sequence:
AGTCATCTTCTATGTTGTGGGCATCCAGTAGTTACAGTCACAGCAMCATT[C/T]AGGGCAAATCCTCCACTGAGACTCGGTTAGACAACTTCCACCAAGGGGAA
Long Flanking Sequence:
CTGTTTTTTTTTTTTTTTAATCCACTTCAAATGTTGACTGTTCTAGATAGTTTTAATAACAGTATATATATTTTTAAAGTAATTAGTAGCTACAGATAGATTAATGTTATGTTGAAGATGACAAATTTATCTTTGCAGTTGCTCACTTTAATTTGCCTTCATCAGGCACTTGAAATTGGTTGAGTTCACTTAAATTCTGTCACCTCATCAGACTGATTTTTTTTCTGCTTGCTTTCATTTCTTTAGGAAAGACCCCAAGTTGGCCTGCCGAGAGCACAGATCGCCACAGCTACTCATGGTACAAAAACCCTTCTGAATGTGACACACGACCTCTTGCCCAGACCACAACATTAAAGTCTGAAAAAACAGAGGACAAGGATTCGTATGATGCCTGGAGCGCTGTGGTTGGTCTAGGGGCACGCTCTACATCCCTCTTTACTGCACCTAAAGAGTCATCTTCTATGTTGTGGGCATCCAGTAGTTACAGTCACAGCAACATT[C/T]AGGGCAAATCCTCCACTGAGACTCGGTTAGACAACTTCCACCAAGGGGAATTTAATGTTCCTGTTGAGCCGTCTGAAAGCGAGGACCACTCTCAGTCTGTGCTCAGGGCGCCTAACTGCAGAACGTACTGCAGACCCAATAAAGGCAAACAGCCTGGTGGAGCTGATGGGAGCGGAAGTGCTTCCAGTCATATCTCCACAGGAGTGTTACAGACCATTGGGACTGACAATGCTAGTAAAACAACGAACAGAGGTCGGACGAGAGACTTTACAGTGTTGCACCCATCTTGTGTATCCATGTTTAACGTCACCTTTCAGGACTCTATGGACCGCAGTGTAGAGGAGTACACAGCCAGCACCCAAGCGTCTGGTCCAGGAGATGAAGGAAGACTGAAGAAGAAGACTGAGACGGAAAGCAAACCTTTGAGGTAATAGCTTGCTAAACTAATATTATTCAAATCATATTAAAGGCATTTCACAGCATTATTTTCAGTTGTTATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13582
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 |
---|---|---|---|---|---|
ENSDART00000032195 | Essential Splice Site | 384 | 1168 | 3 | 19 |
Genomic Location (Zv9):
Chromosome 12 (position 12789992)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 11645645 |
GRCz11 | 12 | 11683948 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTATGAAAGTCTRACTGTNNNNNNNNTTTTTTKTTTTTTTTTTCTGTGGGGTTTCTA[G/T]TCGATCTCGACCCACGCAGAGCAAAATGAAGAGCAGTAAGCTGGAGCTCT
Long Flanking Sequence:
AGAAGATCTGCACTTGAACAGCGTATATTTAAGGGCGCGCAAGAAGTTTTGTGCACGAATAGAAGAAATCGGCGCGCAAGCAAAAAGATTTGCATGTTTGTATTACATAAATGTGATCTCGACTTGTAATGCTGCACTCACAACATTTCTCCATTTGTCATGGAAATAACGCCATGGGTAGTTGGTAGATTTGTGTAACAGACCTGCCGCCACAGCTGGAAAAAATCCTAGAGGAAACACTGGTATATGTATATTATAAGCGATCTGTACACTTCAATTTTGATTATTAAATTTTAATATGATATCGTTTAACGGCCCAGGCCTACCTAACATAAAGTAAAACAAAATCGTGTATATTCAGGTCAAATTAAAATGGAATTCAAGTCAGACTTATGATTCCTTGGTTGCCTCAAATGCCCTCATTCTTTCATGTTTGATTTGAAGTCAACATGTATGAAAGTCTGACTGTTTTTTTGTTTTTTTTTTCTGTGGGGTTTCTA[G/T]TCGATCTCGACCCACGCAGAGCAAAATGAAGAGCAGTAAGCTGGAGCTCTTCGGGTTTGATGACACTGATGCTGTGGCTGACGACGACGACTCTGCTTCAGGAAGCTCGAGCTACAGGATCAAATACTTCGGCTTTGATGACTTGAGCGAGAGTGACAGTGAAGAAGAGGAGGGTTCCTCTCACAGAAGGAGAGCCAAGAGGATGGCAGCGGCCGAGGCAGAGCCTCTGCTGTCTATAGACACAAATGTTGACAGTCCTCCGCCCAGAGAGATGCAGAGCTCCCATAGCAGTTATACTGCAGGTCACAGCCTTAAACACGGTCAGTATTTACACTCAACATTGGAGATTTCTGGAGATCTAGTTTTTGCTTCTGTTTACCTAGCAGTGCCAGCATAAATCCATTGTAAAGCTGAACAGATTATTTTCCCTCTTATCTATCAATGTCTTCAAGAATAGACCTAGTTTGTGTCTATTGTGTGCACCATTATTTCTGTTTATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35225
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000032195 | Nonsense | 432 | 1168 | 3 | 19 |
Genomic Location (Zv9):
Chromosome 12 (position 12790136)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 11645789 |
GRCz11 | 12 | 11684092 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCTTCAGGAAGCTCGAGCTACAGGATCAAATACTTCGGCTTTGATGACT[T/A]GAGCGAGAGTGACAGTGAAGAAGAGGAGGGTTCCTCTCACAGAAGGAGAG
Long Flanking Sequence:
ATTTCTCCATTTGTCATGGAAATAACGCCATGGGTAGTTGGTAGATTTGTGTAACAGACCTGCCGCCACAGCTGGAAAAAATCCTAGAGGAAACACTGGTATATGTATATTATAAGCGATCTGTACACTTCAATTTTGATTATTAAATTTTAATATGATATCGTTTAACGGCCCAGGCCTACCTAACATAAAGTAAAACAAAATCGTGTATATTCAGGTCAAATTAAAATGGAATTCAAGTCAGACTTATGATTCCTTGGTTGCCTCAAATGCCCTCATTCTTTCATGTTTGATTTGAAGTCAACATGTATGAAAGTCTGACTGTTTTTTTGTTTTTTTTTTCTGTGGGGTTTCTAGTCGATCTCGACCCACGCAGAGCAAAATGAAGAGCAGTAAGCTGGAGCTCTTCGGGTTTGATGACACTGATGCTGTGGCTGACGACGACGACTCTGCTTCAGGAAGCTCGAGCTACAGGATCAAATACTTCGGCTTTGATGACT[T/A]GAGCGAGAGTGACAGTGAAGAAGAGGAGGGTTCCTCTCACAGAAGGAGAGCCAAGAGGATGGCAGCGGCCGAGGCAGAGCCTCTGCTGTCTATAGACACAAATGTTGACAGTCCTCCGCCCAGAGAGATGCAGAGCTCCCATAGCAGTTATACTGCAGGTCACAGCCTTAAACACGGTCAGTATTTACACTCAACATTGGAGATTTCTGGAGATCTAGTTTTTGCTTCTGTTTACCTAGCAGTGCCAGCATAAATCCATTGTAAAGCTGAACAGATTATTTTCCCTCTTATCTATCAATGTCTTCAAGAATAGACCTAGTTTGTGTCTATTGTGTGCACCATTATTTCTGTTTATTTCTGATGTTTTCTATATATCTTTTTGTAATCCACTTTTTATGCCAGTCATAGAGATCTTGATCTTCCATATCCTCATAATAATCGAAACTAATGACTAATGAACTTGTGGGGTCATTAGCCAAAACATATCAAGTTCCTTTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35226
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000032195 | Nonsense | 664 | 1168 | 8 | 19 |
Genomic Location (Zv9):
Chromosome 12 (position 12825358)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 11681011 |
GRCz11 | 12 | 11719314 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTTGTAGACCACCTTATTCTTCTTGCTTCTGTTTGCAGTGTTATTAGTT[T/A]GGCCACGCGTTGCGCAATGCCCAGTTTTAGAATGCACCTGAGGGCTCGTG
Long Flanking Sequence:
GTGAATATGGAATGACGAAGCATTTATATTTCTTAAAAATGAATATAAATTATTTATAAGAAATAATAATATAACAAGGTCTTACTTGTCATGTTTATAAAAAAAAAATATGACCAATAAGGCAGATGCTCTATTGCCATCATGAATCTAACATTCGCTGTGTGATCCTGCCTTTTGAGTGCATGCTCTGGCAGATGGTTACTGAATCAATAAAATAGCCATCAACATGCTTGCTCTCTCCGCAGTTGTACACAGTTGTTCAGCATGTGAAGCACTTCAATGATGTGGTGGAGTTTGGTGAGAATCAGGAGTTCACAGATGACTTTGAATATCTTGCCACTGGTCTGAAGACTGGACAACCCCTCAACACACGATGCCTTAGGTGCAGAAAACCTTTCATCTTTAAGCATTCAAACCATTTTTAAATTTTTAAACCGTGACCTCATGTTTGTTTGTAGACCACCTTATTCTTCTTGCTTCTGTTTGCAGTGTTATTAGTT[T/A]GGCCACGCGTTGCGCAATGCCCAGTTTTAGAATGCACCTGAGGGCTCGTGGAAAAGTGGCCCAAGTCTTTAAAACTCTCGGTGATGCACCCCAACATTCAGTAAGTTCAAAATAGTTTTGACTTATTTCAAATGTTCAGTGGTTGATGTTTTGTTTATAACTGATTTTGTTTTGTTTTTCTTTTCCTCTTTTTTAGAATCTAGCTCTGTGTACGGCCTCTCTTATGTACATTCTCAGCCGAGATCGCTTGAACATGGACCTGGATCGGGCCAGTCTTGATCTTATGATCCGATTACTGGAGTTGGAACAAGATAAATCCATCGCTGATCAGTTGACGACAAAAGAGATGAATAAAGTGAAAGAAAAGATTCGCAAACTCTGCGAAACTGTCCACAATAAGCATCTTGATTTGGAGAACATCACAGTAAGCTTGAAATCAGATTTTGCTTCTTTATTGTGCAATAGTCATTTTTGTGGGCTTTTTCATTGCGTTCCCTACC
Associated Phenotype:
Not determined