ZMP
Q58EF5_DANRE
Ensembl ID:
Description:
KIAA0261 protein [Source:UniProtKB/TrEMBL;Acc:Q58EF5]
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 |
---|---|---|---|
sa42941 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa45608 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa12782 | Nonsense | Available for shipment | Available now |
sa42942 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa42941
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000064817 | Nonsense | 3 | 1062 | 2 | 17 |
ENSDART00000122105 | Nonsense | 3 | 1153 | 1 | 19 |
Genomic Location (Zv9):
Chromosome 17 (position 25699994)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 25839913 |
GRCz11 | 17 | 25858304 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACGTGTTTTACTTCTTTATAGATAATATGTAACAAGCGACAAAATGACAT[C/A]AAGATTTAGTAAAACGTACACGCGGAAGGGAGGAGAAGCCAGCTCAAAGT
Long Flanking Sequence:
TCAACTTCTATTTGGTTTAGTCCCAGAGCTCTGAGGGTCAATGAAGATTATAAATGCATTTATTTGTGTACAGTAACCAAGAAGAAGATGACAAGTAACGGCAGTCCTGAGCTTCATCAGTCTATATTATATGTTTTCTAATATTCATCAGTCTATATGAATTCATGGAGTCTAAAAATATATAATATATTTTATTTAATATATAAACAATATAATTTTTAGTCATATTTGCCTGAAGGTTTATATTTTAAGAATTCTATTTAAGTGGCTTTCAGTTGCTAAAATTTATTATTCAAACACGTTATATCTAACAAGTTCTAACTTCTAAGACATCTAAGAAAGGTTTATATATCAAGTTTGTGTATTTCAGTTTCACTGTAGCATTTAGAACTAAATGTAAACCTCCTTGTTCCTACATAATCCAAGTTTGATAAGTTAACCTTTATTTTAACGTGTTTTACTTCTTTATAGATAATATGTAACAAGCGACAAAATGACAT[C/A]AAGATTTAGTAAAACGTACACGCGGAAGGGAGGAGAAGCCAGCTCAAAGTTTGACGAAGTGTTCTCTAACAAGAAAGCTACACTCACCACCAAATGGGGAGAGTCCACCTACAAGGCGCATTTGGGCATCAAACGACCCTCATTCAAGCCAGATGTTTCAGAGCTGACCAAACGACCCCGCTTTGATGATGACGACAGCTCAGAGGATCCGTTTGGCTTTGACAGCGATGATGAGTCCAAAACAGTCACATCCAGAGATACTGCTCAATCTGAGATGGACTCGGATACTGCAGGACCCAAGAATGAGCAGTTAAAGACCCGGATGGAAAAGCCCAGCGGGGGGACACTGGTGACCAGTACTTCTTCCTTGGGGAGTAGTACAAACATCAGCAGAGGGGCGGTTGGCGTGAATAGCCCAGGTAAGAAATCTGTTAAATCAGCGCATCATTATTGCAACAACACTTGTGTGGGATATTGTACACCAATATGAAAATGATCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45608
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 |
---|---|---|---|---|---|
ENSDART00000064817 | Nonsense | 44 | 1062 | 2 | 17 |
ENSDART00000122105 | Nonsense | 44 | 1153 | 1 | 19 |
Genomic Location (Zv9):
Chromosome 17 (position 25700117)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 25840036 |
GRCz11 | 17 | 25858427 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAAGCTACACTCACCACCAAATGGGGAGAGTCCACCTACAAGGCGCATT[T/A]GGGCATCAAACGACCCTCATTCAAGCCAGATGTTTCAGAGCTGACCAAAC
Long Flanking Sequence:
ATATTATATGTTTTCTAATATTCATCAGTCTATATGAATTCATGGAGTCTAAAAATATATAATATATTTTATTTAATATATAAACAATATAATTTTTAGTCATATTTGCCTGAAGGTTTATATTTTAAGAATTCTATTTAAGTGGCTTTCAGTTGCTAAAATTTATTATTCAAACACGTTATATCTAACAAGTTCTAACTTCTAAGACATCTAAGAAAGGTTTATATATCAAGTTTGTGTATTTCAGTTTCACTGTAGCATTTAGAACTAAATGTAAACCTCCTTGTTCCTACATAATCCAAGTTTGATAAGTTAACCTTTATTTTAACGTGTTTTACTTCTTTATAGATAATATGTAACAAGCGACAAAATGACATCAAGATTTAGTAAAACGTACACGCGGAAGGGAGGAGAAGCCAGCTCAAAGTTTGACGAAGTGTTCTCTAACAAGAAAGCTACACTCACCACCAAATGGGGAGAGTCCACCTACAAGGCGCATT[T/A]GGGCATCAAACGACCCTCATTCAAGCCAGATGTTTCAGAGCTGACCAAACGACCCCGCTTTGATGATGACGACAGCTCAGAGGATCCGTTTGGCTTTGACAGCGATGATGAGTCCAAAACAGTCACATCCAGAGATACTGCTCAATCTGAGATGGACTCGGATACTGCAGGACCCAAGAATGAGCAGTTAAAGACCCGGATGGAAAAGCCCAGCGGGGGGACACTGGTGACCAGTACTTCTTCCTTGGGGAGTAGTACAAACATCAGCAGAGGGGCGGTTGGCGTGAATAGCCCAGGTAAGAAATCTGTTAAATCAGCGCATCATTATTGCAACAACACTTGTGTGGGATATTGTACACCAATATGAAAATGATCATACACGAGTAGACATCTCAAGTTATTTCAATTCTGTATGACTTGCTTTGTTTTTTGTGCTAAGGGTGTTCAGAACTGGTTAGTGAATGATTCATTCTTCAGTTTTGTGAACTAGATCATCTAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12782
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 |
---|---|---|---|---|---|
ENSDART00000064817 | Nonsense | 48 | 1062 | 2 | 17 |
ENSDART00000122105 | Nonsense | 48 | 1153 | 1 | 19 |
Genomic Location (Zv9):
Chromosome 17 (position 25700128)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 25840047 |
GRCz11 | 17 | 25858438 |
KASP Assay ID:
2261-1111.1 (used for ordering genotyping assays)
KASP Sequence:
TCACCACCAAATGGGGAGAGTCCACCTACAAGGCGCATTTGGGCATCAAA[C/T]GACCCTCATTCAAGCCAGATGTTTCAGAGCTGACCAAACGACCCCGCTTT
Long Flanking Sequence:
TTTCTAATATTCATCAGTCTATATGAATTCATGGAGTCTAAAAATATATAATATATTTTATTTAATATATAAACAATATAATTTTTAGTCATATTTGCCTGAAGGTTTATATTTTAAGAATTCTATTTAAGTGGCTTTCAGTTGCTAAAATTTATTATTCAAACACGTTATATCTAACAAGTTCTAACTTCTAAGACATCTAAGAAAGGTTTATATATCAAGTTTGTGTATTTCAGTTTCACTGTAGCATTTAGAACTAAATGTAAACCTCCTTGTTCCTACATAATCCAAGTTTGATAAGTTAACCTTTATTTTAACGTGTTTTACTTCTTTATAGATAATATGTAACAAGCGACAAAATGACATCAAGATTTAGTAAAACGTACACGCGGAAGGGAGGAGAAGCCAGCTCAAAGTTTGACGAAGTGTTCTCTAACAAGAAAGCTACACTCACCACCAAATGGGGAGAGTCCACCTACAAGGCGCATTTGGGCATCAAA[C/T]GACCCTCATTCAAGCCAGATGTTTCAGAGCTGACCAAACGACCCCGCTTTGATGATGACGACAGCTCAGAGGATCCGTTTGGCTTTGACAGCGATGATGAGTCCAAAACAGTCACATCCAGAGATACTGCTCAATCTGAGATGGACTCGGATACTGCAGGACCCAAGAATGAGCAGTTAAAGACCCGGATGGAAAAGCCCAGCGGGGGGACACTGGTGACCAGTACTTCTTCCTTGGGGAGTAGTACAAACATCAGCAGAGGGGCGGTTGGCGTGAATAGCCCAGGTAAGAAATCTGTTAAATCAGCGCATCATTATTGCAACAACACTTGTGTGGGATATTGTACACCAATATGAAAATGATCATACACGAGTAGACATCTCAAGTTATTTCAATTCTGTATGACTTGCTTTGTTTTTTGTGCTAAGGGTGTTCAGAACTGGTTAGTGAATGATTCATTCTTCAGTTTTGTGAACTAGATCATCTAATGTATTGAAGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42942
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 |
---|---|---|---|---|---|
ENSDART00000064817 | Nonsense | 760 | 1062 | 11 | 17 |
ENSDART00000122105 | Nonsense | 760 | 1153 | 10 | 19 |
Genomic Location (Zv9):
Chromosome 17 (position 25714717)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 25854636 |
GRCz11 | 17 | 25873027 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGGTCATTTAGCAATGGAAACGCTGCTGTCTCTGACGTCGAAGCGAGCT[G/T]GAGACTGGTTTAAGGAGGAGCTGCGTTTACTTGGGGGACTGGACCACATC
Long Flanking Sequence:
ATATTGCAGAAATGTATATCGCAATGTCATATTTTTCCAATATTGTGCAGCCCTATTTCATGTTATTATAAATGCTGAAAACATTGTGCATTTTAAATATATTTGTGTTATAGCTTCACAAACTTTTCAGGATACTTCAGATAGAGTAAAAAAACAAGACTCAATAAAATGTATTACAAAAATATAAATGTCATTACAGTCACAATCAGTTCCTTGCATTCTTACTGTGAAAAAAAAATATGTGTGGGTGTGTATGTGTGCATTTCAAAAATTAACTGACCCAAAACTTTTGAACTTGTGTAACAGGCCTGTTAGATAAGTGTTTTTGTCAGTTCACATTTATAAAGTGCTACTAAAGTAAAAAAAAAAAAAACTAATTGCAAATAATTGTATTATTTATTTTTATTTTATTTTTTACTTTATGTGCTCATCTCATTTCTTAATTTCAGACTGGTCATTTAGCAATGGAAACGCTGCTGTCTCTGACGTCGAAGCGAGCT[G/T]GAGACTGGTTTAAGGAGGAGCTGCGTTTACTTGGGGGACTGGACCACATCGTAGATAAAGGTGTGTATCTCTTTTCTGATTTATACATTGTGTATATCGCTATCTGATTTATATTTGTGAAAGGAATGGTTAGCAATGACTTTTTCTCCTCAGTAAAAGAGTGTGTGGAGAACTTGAATAAAGAAGAAGATAAAGAGAGTCTAGTGGCGTCACTCTGGGGAGCAGAACGCTGCTTGCGAGTTCTGGAGAGCGTGAGTGCACAACATGCTAGATGATCAAATCGTAATTGGTGTTGCTTTTCTTTGAAAATGCCTGCAGTAATTGCATAATATCACAGACTGTAGAATAAAGTGTTGTCAATGTGTAAAAAATAGAGGCTGAGAGATATACAAATCAAGTACTTAAGCAAAAAAAATAAATAAATAAAGTCCTAAAAATAAAAATTAAGTATTTGCATTAAGCAAATTATATTCTAATATTATAATTACTTGATCATTTTA
Associated Phenotype:
Not determined