ZMP
wasf3
Ensembl ID:
ZFIN ID:
Description:
wiskott-Aldrich syndrome protein family member 3 [Source:RefSeq peptide;Acc:NP_001074059]
Human Orthologue:
WASF3
Human Description:
WAS protein family, member 3 [Source:HGNC Symbol;Acc:12734]
Mouse Orthologue:
Wasf3
Mouse Description:
WAS protein family, member 3 Gene [Source:MGI Symbol;Acc:MGI:2658986]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa24495 | Essential Splice Site | Available for shipment | Available now |
sa44132 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa37881 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa44133 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa14506 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa24495
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000091529 | Essential Splice Site | None | 481 | 1 | 9 |
Genomic Location (Zv9):
Chromosome 24 (position 22148934)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 21395812 |
GRCz11 | 24 | 21540986 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAGCCTGGACATGTGAGCGAATACAATTCTCTACAAATTTCACTTTTGG[T/A]AAGTCTTCAACGTGCACTAACCTCCCCTAATGTACTTATTTGTTTATATT
Long Flanking Sequence:
GTTTTGATGACAACCAATCAACATATTCAATCAACACTTCCCCCATCACCCGCGGTAAGTGGACCATTTGCTTTTTTAGGCTTTTTTTTGAACGTCCCATTTACCAAACGTTTGACGCACAATGGTCTTTAGTAAATCTCTTGTTTTATAAGAAGTAGAACTTCATTACTTTAATGAATCATTTAGCTGTGATGTTTTTAAAGCCCACCTAATATCCCCAGATAAATCCCGCCTTCACACAGCCGCCCAATGATTTAATGACCGGGGGACTCTCTGTCAATCATCCTTTTCCCCGCATCTGATAGGCTGAGTGTGACAAACGGTGGCGCGTTAAATTCTTATTCCAAAATGCTGATTGGTGCGAACTACCCGACATGCCCCGCCCCAAGCGGATTGTTTGGAATGGTCAGATGGACCGATGGAGACACAGGATGGCAATCCGGACCGCTGAAAGCCTGGACATGTGAGCGAATACAATTCTCTACAAATTTCACTTTTGG[T/A]AAGTCTTCAACGTGCACTAACCTCCCCTAATGTACTTATTTGTTTATATTACACTTGCTATGTTTACTATTTATCGAGCTTTATGTAATAAGTGGAACATGAGGTTTGGGTTTTCGTTGTTTTGATTTGTGCATTTAATTATTTTTGAGATTTTTGTGTTATTCATAGTTTATTATACTAAAGTACAATAGTATTATTGTTGTTATAATAACAATAACAACCTTTGCCTGCTTAATACCAGAGTATGTCGTCATTGGAATAATAATGGCAAACAAAAGTTACATATTTTCAATTAAATCAACACAATAGGCTAAATACTAAAACCTACGAAGACCAAATTATACCACAAAACATAATTACAGAAGTTTCACTGATAAAGTGATTACTAAATAACGAAACAGTCAATCGATTAAATTACGCTATTTCTTAATATAAACGCCAGCGTTACGCGCGGTTTTACAGCTCGTGACATTCACAAGCCTTCATCATGTGTGACGTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44132
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 |
---|---|---|---|---|---|
ENSDART00000091529 | Nonsense | 88 | 481 | 3 | 9 |
Genomic Location (Zv9):
Chromosome 24 (position 22169053)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 21415931 |
GRCz11 | 24 | 21561105 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCGCATTGACCGTCTCGCCGTCAAGGTCACCCAGCTGGACTCCACCGTC[G/T]AGGAGGGTGAGTGTTTGTGCTTCTGTGAAACAAGAGCTGCGTCGCTCGCC
Long Flanking Sequence:
AATTAAATAATTACAATTTAATAATTATAATAATAATTTTTATTTAGCTGATTATTTCTTCATTTTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACATAAATTTCCATTTACATATCCCTTTTTATTATTACATTATTGGTGTTAATTGTGTTTTGTTTACATTTTAAAGTGTACCTTTTTACCAAGACAACAACAGTGTCGGCTAAGATTTTTAAGTGAAAAAAAATTAAACGTATTCACATTATATTATGCCATTTGTTCCCTCGTTTTTAACCTGATCTGTTTCCCTCATGAATGAATCTTCAGCTAACTCTTCTCTTCTCCCCAAGGTAAACATGCTGAAGACATATTCGGCGAGCTCTTCAACGAGGCAAACATGTTCTATTTGCGGGCGAACTCTCTGCAGGACCGCATTGACCGTCTCGCCGTCAAGGTCACCCAGCTGGACTCCACCGTC[G/T]AGGAGGGTGAGTGTTTGTGCTTCTGTGAAACAAGAGCTGCGTCGCTCGCCCATTCACTCATTCACTAATCATCGCTACATAATGCAGAACAGTCGAGTGAGTGGATGATATCAGGAAAAGAGGGAATAAAATTGAATGAGTGAATTCAGATGCTCACATAAAAAGCATGAGTCTGACCATGAGCTTGAATATCACTACATTTATCACATTCATTGAATTCATTATAACAAAGAAAACAACAGCACCTGCTCAAAGTCCCTTTAAGGCAGGTCATGTCACTCGGCGACCATCTTTGAAACATCTCTCTGTCATTTTGTTTCAATGGTGAAACATCAAATTTTCCAAAACTGTTTGCCAAGCTTGCACTTAAATTTCATAGTTGGAATCATCAAAGAGATTAAACAACACTGTCTCTTAAGTTTAATTTCTAAACATTTGAATCACACAAAATTAGCATATTTTTTAGGTTACCCTAGCTAATGCGCATGTTCACTCAATGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37881
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 |
---|---|---|---|---|---|
ENSDART00000091529 | Nonsense | 107 | 481 | 4 | 9 |
Genomic Location (Zv9):
Chromosome 24 (position 22171466)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 21418344 |
GRCz11 | 24 | 21563518 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTCTCTGCAGGACATAAACATGAGGAAGGCGTTTAAGAGCTCTACTATA[C/T]AGGACCAGCAGGTGGTGTCCAAGAGCAGTGTTCCCATTCCTGTGACCGAG
Long Flanking Sequence:
ATTGAACAATGGTTAATGTGATAGTTCACCCAAAATGAAAAATCTGTGGTTATTTACTCTTCAAAAGAACAAAAAACTCAAACTCAAGTCAAGGTTGAGTCAATTATGACATAACTTTAATTTTTGTGTATATTATCCTTTTGATATTTGTTACATTTATTGCATAGTTATGGAAGAGAATACAGTATTTTGCCTGTTAGTACATCTGTGTTTATCCTCATTTACACACTTTGTTTGATAAAATGATTCAATTGCATTTCTATCCATGTTCTAAATAGAGATAGTCTTAATTAAAAGCAAAAAAAAAACATCTGGTTCTGACTTGTGGGATGACTCGGATCTGTGCGTCTCTAGAAGTTATTTTTATTTTTTTCAATTAAAAGATCAATACTGGAGTTTACTTTACCCTCTCTGGAGGCCGCGGGTAATGGATCTCTCTCCTTCTCACAGTCTCTCTGCAGGACATAAACATGAGGAAGGCGTTTAAGAGCTCTACTATA[C/T]AGGACCAGCAGGTGGTGTCCAAGAGCAGTGTTCCCATTCCTGTGACCGAGATGTACAATCTGAGTGATAAACCACCACCGCTCAATATTCTCACACCCTACAGGTATGTGCCTGTGTGTGTGCGTTTGGGATTTTTGATTTTTGGGAAATATTTGACGTAATGAACAATGTTAAATATTTTTCAATCAATTTCCAATTTATCAATAGTTTTCATTTTAATTTACAATCGATTTCACTTACTTAAAATTGACATGGAATTTTATTTTGTTTAAAAATAATTTTATCTAAAGTTGAAATCAAAATTATTAGCCCCCTGTTTAATTTTTTCCCCAATTTCTGTTTAACAGAGAGAAGATTTCTTCAACACATTTCTAAACATACTAGTTTTAATTACTGATTTCTTTTATATTTGCCATGATTACAGTAAGTAATACATGACTAGATATTTTTCAAGACACTTTTATACAGCCTAAAGTAACATTTAAAGGCTTAACTAGGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44133
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 |
---|---|---|---|---|---|
ENSDART00000091529 | Nonsense | 221 | 481 | 6 | 9 |
Genomic Location (Zv9):
Chromosome 24 (position 22176814)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 21423692 |
GRCz11 | 24 | 21568866 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCAGGAGTGGAACATGATGGCCTTCGATAAGGAACTGAGACCTGACCTT[C/T]GACATTCACACACTGTACACAGAGGAGGATCCACAGAGGGCACCATGTCC
Long Flanking Sequence:
GATAAATGATGTTGTGCTCAATGCCTACCAGAATTTCCCACTAGAGCAAGTGACATCGCTTGGAGAAAGTCACTTTTTCTATTAGAGCTTTACAAATTGATATACCTTTTTAACTGATGTAACAGTTGACCAGAGCATAAGCACAGAACTGAAATTACAAAAAAAAAAGAAATGTTGCAGAAATTGTTTATTTAGCTTAGTAAACACATAAAAAAAATCTACTTAAATTATGATTATATTACATTATGTAATTACATTATATTAATAATCATTGTAATCCCTTGACAGCCCTAATGTTTATATGCGTAATTTTTTGTACAGTTCTATATATCTATGTTGGATAATTCAATTTCTCTTTGTACTTTCACACTTTGCTTCAGGAGCAGAGGCGATGTGTAGATGGCACACTGCAGAGAGAGGTGAAGAAGGTGCGAAAGGCACGTAACCGCAGGCAGGAGTGGAACATGATGGCCTTCGATAAGGAACTGAGACCTGACCTT[C/T]GACATTCACACACTGTACACAGAGGAGGATCCACAGAGGGCACCATGTCCCCAGAGCACAGGTAACACTGGCTGTATACGCTTAAAGTGACAGTTCACCCAAAACTGAAACTTTACTGGTAATTTACTTACCCTCAGGTCATTCAAGGTGTATATTAATGATGATTTTTAGCTGAAACTGTGGTCCGTGGTGATTAATGTAATGCTCATCAGTGACTACCAGCACTTTGAGGGTAAAAACATGTATAGGCAAAACAACATTATTTATTATTAGTGCTGTCAATCGATAAAAAAAATTAACTAATGAATCGCACCTTTTTAAAAAAAATTAATCGTGATTAATCACGATTAATCGCATTTAAAATACTGAAATTTGTAATTCTGGCTATTTAAATGTAAAATTAATGTAAACGCAAGACAAAAACTATTTAAATTCAAAATATAATTGTTTATAAGAACTAAAATTCAAACTATAATTGTTTAATAGAATTTTTGTTTAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14506
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 |
---|---|---|---|---|---|
ENSDART00000091529 | Nonsense | 293 | 481 | 7 | 9 |
Genomic Location (Zv9):
Chromosome 24 (position 22180594)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 21427472 |
GRCz11 | 24 | 21572646 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CATACTCAKATGAGCCTGGATCAGGATTACCGCAGCGGGTCAATGGCGTA[T/A]CGTWCTGGGACTCTCGGTCGCCCACATCAGGCTCCACCTCCTCCACCAGC
Long Flanking Sequence:
TTCTAAATTTGTTTTGAAAAAATTAACCATTTGCTTGCCTCTGGAATTGCATTCCTTCTCTGACGAAAAATCCTTAGCCATGCCCCTCCAACCGTTATTTTTGTTATGAGTAAAATGTAAGAGGAAGAGCTCAAAAGTGCAATATTGAGTAGGGGGTGAAGTTTTATTTCAGTTGGAAATATGTCATAATATTAAAACATGTCTGCCACAAATTTTTACTGACGGAAATATGTATTTAGATCTACGAAATTAACATCAGTTGTTCATTTTTGGGTGAACTATTCTTCAAAGTGCACATATACCATGAACTCGTTTTCATTTTTTCTAATTGGTAATTGGCACAGGTCTCACGGAGATCATGCAGATCACGGTTATCTGTCCATGGCCAATCACGTCGGTCATGCCCACACCTACTCTGGGCCTCCTCCCAGTATGGCGGCTCTGTCAGCTCATACTCAGATGAGCCTGGATCAGGATTACCGCAGCGGGTCAATGGCGTA[T/A]CGTTCTGGGACTCTCGGTCGCCCACATCAGGCTCCACCTCCTCCACCAGCATCACACACCATCAACGGCTCCATGACCCTCCCACCTGTCGACTACAGGTTTGACATTTTTTAAAGCGATTGATAAATAATATCTAATGTTTTGAAGTAACTATTAACGTATTAGTTTCACGAGTAGATAAACTAAAATGTAATACTATTAACAATGCTTAAGTTTTGTCTTTTTTTTTCATTTTTAGATGTCTGTGTAGTTTGTATTGTGGTCTATTTGTTTTTAAGATCACCTAAAAGAGAAGATGAGATGTATTTGCACCAAACTATATCACAAGTTTGAAATGAGAATGATTTATAAATCAAAAGAGAAGCAGTTCATGCAAAATGTTTCTAAATTGTGTTAATTTAGCAGTTTTACTCTTGTTAACAAAAATGAATAAATGTATTATTATTTTTTTTTCTTACAGGTATTATTAAATAATTAACTATTCAATAGTAATATTTCTT
Associated Phenotype:
Not determined