ZMP
vwa2
Ensembl ID:
ZFIN IDs:
Description:
Vwa2 protein [Source:UniProtKB/TrEMBL;Acc:D2DUP6]
Human Orthologue:
VWA2
Human Description:
von Willebrand factor A domain containing 2 [Source:HGNC Symbol;Acc:24709]
Mouse Orthologue:
Vwa2
Mouse Description:
von Willebrand factor A domain containing 2 Gene [Source:MGI Symbol;Acc:MGI:2684334]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22127 | Essential Splice Site | Available for shipment | Available now |
sa22126 | Essential Splice Site | Available for shipment | Available now |
sa18645 | Essential Splice Site | Available for shipment | Available now |
sa15844 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa22127
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 |
---|---|---|---|---|---|
ENSDART00000113860 | Essential Splice Site | 33 | 740 | 1 | 11 |
ENSDART00000128459 | None | None | 38 | None | 2 |
ENSDART00000130199 | None | None | 260 | None | 3 |
ENSDART00000113860 | Essential Splice Site | 33 | 740 | 1 | 11 |
ENSDART00000128459 | None | None | 38 | None | 2 |
ENSDART00000130199 | None | None | 260 | None | 3 |
Genomic Location (Zv9):
Chromosome 12 (position 31908869)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 30218212 |
GRCz11 | 12 | 30333114 |
KASP Assay ID:
554-4404.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATACAAACGGATCTTGACACCATTATGAAGATCAACGCTGCTGGAGAAAG[T/A]GAGTTTTGGACTTGAAAGCAATGAGTTGTGTTCATCAATGAGTATGTTTA
Long Flanking Sequence:
GTTTACATTTTTAAAATTTTTTAAATACATGTTTTACCATTTATATACTTAAACCGTAAAGAGTATTTACAAGAATCGAGGCTAATGCTTTATTGTTATAAACTTTACTGTTTGTAAAAAACAGTTGTAACTTTTTTTGACAGACATCTAATTTTATTTATTTATTTATTTATTTAGTTTGTTTGCAAAATTTCTGATATATACTGTCCTCTACAGTTTCTTAATGGAATAGAAATATCTTTTTAAAAGAGTCTTATATAAAATGGGTGATTCAATTTTATTTTTTTCATTCATTTATTAATTCATTTATTTGCTCCGTGTTCTCTCTCTATACATATATATCATTTTATTGTAAAGATATATCACGTTTAGTTTGGGTGTTAATCTACAAACTCTACTAACTACAGTATTTCTTTCTTTAAAGTTTGGTCCATTTTCTCTGTGCAAGAAATACAAACGGATCTTGACACCATTATGAAGATCAACGCTGCTGGAGAAAG[T/A]GAGTTTTGGACTTGAAAGCAATGAGTTGTGTTCATCAATGAGTATGTTTACATGGACACCAATAATCCGATTTTAATACGATTAAGACAACACTCTGATTAAGAGTCTACCATGTAATTTTTGATTTATTTAATCAGATTAAGGTCATAATCGAACTAAACAGAAATTGAATTAAATCATGTGGAGTATGCCGATTTTAGTCACATTATTGCAGTGCAGCACAGACATGTAAACGCTGCAAATATTACCGTCATGTAAGACTTGTTGCTGCGGTTTGTGACAGGATACTCTATACAAACACGGCTGTTCAACACTATTCTCTGCAACTACCGAGTCAGTGAAGGAACATTGGGCGTGCGGGATCAAATTCTATTAAAACAACACTCTTCCACTTGTCCTTACTTCATTCGCACATCCAATACCTCAGTTTGTCATGTGGGGGCATGAATGAAGTGTTCCTAAATAAAAGTAAAACTGCCGTACTGCATTAAACACCCAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22126
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 |
---|---|---|---|---|---|
ENSDART00000113860 | Essential Splice Site | 77 | 740 | 2 | 11 |
ENSDART00000128459 | None | None | 38 | None | 2 |
ENSDART00000130199 | None | None | 260 | None | 3 |
Genomic Location (Zv9):
Chromosome 12 (position 31906745)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 30216088 |
GRCz11 | 12 | 30330990 |
KASP Assay ID:
2260-5530.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACACTACATGTTGAAGCTTTGTGAGGCTCTTGATGTCCGCCAAGACAAG[G/A]TCAGACTGGATAAAGTCTATTTAAGATAGAAAGGTTCACCCAGAATTAAA
Long Flanking Sequence:
GTTCTCACTCTCACACCTAAAAGTGTGCGTGTGCTGTTGCAGACAGCGGCGTGCCGTCTCTGTCTAATCACCTTCTTTATGACAGACGGCGGGTTCTAACATGACAGCTACATGGATTATAATTTAGGCACTTGACTAGCACAAACTTGCTGTAATGTGTTTGTGAGTATTTATCTTTGCTAGAACATGCCATGGGCGACCTTTGAGCTCTTAAAATGTGTCAAACACAGGCCATCGTTTGTGTCAAGTGTTGCTTTTTGCCCTACCGCCTATATTATGTTTCATCGGAAAACTCTTGACTTTTCATAATTGACCATTCAGTTGCCAAATATGGAGTAAGCTTTGTTTTCTCTTGTGCTTGGTCAGTGATGCAGTGCTCTGCAGCCATGGATATCCTCTTTGTGATGGATAGTTCATACAGTGTTGGAAAAGGAGGGTTTGAGAGATCCCGACACTACATGTTGAAGCTTTGTGAGGCTCTTGATGTCCGCCAAGACAAG[G/A]TCAGACTGGATAAAGTCTATTTAAGATAGAAAGGTTCACCCAGAATTAAAAAAAAAAACTATCAGCATGTGTTCTGTCTGTATTTGTTTCAGTGCAATATGTTATAGTTTCCATTTATGAATTTTGTATACTCTTTAAAAAACAATATTGGATTCAATGAATACGTACTAGACCGATCACAAGACTTACTAGTCATGGTTTGGATCATTTTTTTGTGGAGTGGGCAAAACAAATGGGTAAACTTAATTTTGCTTTTCACTTAAGGACCCTTATCACAAGCCTGCTATGATGCGTTCAACTTTCATCAACATTTTAAATCTTTGAGAAAATCAAACAACAAAAAATGAACGTTGTTCTTTCTTTTGGCTACAGTTATCAGTTTCACAGTATTTTTTCCTTTCTTTGAAAGTCTTGATAACACCATCATGGAGTTTTTCTTTTATTATTTCAGCAAATAGTTTTGTAAAAAATAATTTCTTGGACTTTCTCATTCACCAACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18645
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 |
---|---|---|---|---|---|
ENSDART00000113860 | Essential Splice Site | 514 | 740 | 9 | 11 |
ENSDART00000128459 | None | None | 38 | None | 2 |
ENSDART00000130199 | None | None | 260 | None | 3 |
Genomic Location (Zv9):
Chromosome 12 (position 31892685)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 30202028 |
GRCz11 | 12 | 30316930 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGCAAGATCCCAGAACTAAGAGCCAAAATYTGCAGCGTCGACAACCAGG[G/A]TAGAGAGCTAATCTATTTTTYATTGTCAMCACAGGAAAGTCTTTAAAAAT
Long Flanking Sequence:
CTTGCGATTCAAGTCCTTCCTGAAGCGTTTCATGCAGGCCGTATTGAGCTCTGACACTCCTGTAAAAATGGGGTTGGCCCAGTATGGCAGCGACGTGAAGATCGAGGCCAGAATTGGGGAGCACAGAGACCCGGTGAAGCTGATCCAGGCTGTTGAGGGACTTCAGTATCGTGGTGGGCAGACGAAAACCGGAAATGCCCTTCGCTACATCACACGCCACGGCTTCCAGAGCACGCCTGTGTTCGCTGACGTTCAGGACGACCTGCCGCGGGTGGTAGTTCTGCTCACCGGGACGCCCTCAGCAGATCATGTGGTGGAGCCAGCGAAGTACGCACGGGACAGGGAGATCTTCATCATCGGTGTAGCGCCAGAAGGCATGAGGGCTGAGATAAACAACATCACAGGGAACCCTCAGCGCACCATCATGTACCAGTCACCGGATAGATTGAGCAGCAAGATCCCAGAACTAAGAGCCAAAATCTGCAGCGTCGACAACCAGG[G/A]TAGAGAGCTAATCTATTTTTCATTGTCAACACAGGAAAGTCTTTAAAAATGCAGAGTTTGGTGTGCCTCAGGGAACAGTTCACTCATTTTTTTTGTATCCAGTGTAAATTAACAGAGAAGAGTCAAACACTGACAAAAAGAAACTCAAGTTGTTTGTATTTGTAGAAAATTACTAAAAAATCTACTGTACTGTACTTACAAATATTGATTACTTAAAAATCATTATGGTAAAAAATCAATCTTAAAACATTCTGTTTATGTAAGAAAAAAAAACAAGATTATTTGGTATACACTTAGAAAAAGTTGTAAAGTAAGTGAAGCTAAAGGTTTTGGACTTTACACAGGAATGCAAAAGTTGTAAAACCTTCAATAATATTAATAAAAAAGGTCTTGTAAAAACTGCTTTACAGAGGAACAGAAATCTACGAGAACTCGATTAATTAAAGTTTCTTAGGGAAAAATTATGTTTTGTTAAACTTAATTGTAAAAAATGTAAATGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15844
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113860 | Nonsense | 535 | 740 | 10 | 11 |
ENSDART00000128459 | None | None | 38 | None | 2 |
ENSDART00000130199 | Nonsense | 18 | 260 | 1 | 3 |
Genomic Location (Zv9):
Chromosome 12 (position 31890821)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 30200164 |
GRCz11 | 12 | 30315066 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
RTCAGGCTCTGGACCTTGTGTTTGTTCTGGATGCCTCCAGTGGTRTYGGC[A/T]AGGAGAATTTCATTCACTTTCAGGATTTTGTTCGGAGCACTTCAGTGCAG
Long Flanking Sequence:
GTGTACTTTAGTAAAAACAGTATGTGAGCAAAGTAGTATGTCCAAATTTAAAGAGTTCGGATGACCTACTACTTCTGGCTAGATTCTGAAGTATGTATCCGATCGACGCTATACTATCCCATGATACACACCGAAAGAATTCATAAATGAGAGTCAGTTGACGCAACTGACTCAGGTAGATCACATGGTAATAAAATGGCGGCTGTAGTACCTCCAGGTTGCATTTATACTACTCCCATTCATACTATTTAGAACGGTCATGTAGTAAATTCGAATGTAGTAGTTACTGAGTAAGTAGGCGATTTCAGATACAGCCTATGTGTTTTGCAGCAGCATAGCTGATCTAGTCCTCCAAGACCAAACTATGTACATTCTATTTTTAAATTCTGTACATTCGGAGTTGTCATGACTGAACTATTATACCCCTTTTGTTTCTGTTAGGTTGTCTGGGTCAGGCTCTGGACCTTGTGTTTGTTCTGGATGCCTCCAGTGGTGTCGGC[A/T]AGGAGAATTTCATTCACTTTCAGGATTTTGTTCGGAGCACTTCAGTGCAGTTTGACATTAATCGAGATGTGGCTCAGGTGGGATTGGTGGTTTATGGGAGGCGTCCAGTCACGGTCTTTGACTTGGACAAGTACAATTCGGGCTCCGCTGTGCTGAGGGCTGTGGGGGACGCCGCTTTTCTGGGTGGGAAGGCTTCTGTAGGTTCAGCCCTGCTCCATGTGCTCTCCCAAAGCCTGACGGTGGGGAAGGGAGCACGTCCTGGAGTCAACAAGGCTGTGGTGGTGCTGACTGATGGGACGGGTGTGGAGGACGCTGCGGTGCCTGCACAGAAGATCCGTGATAGCGGAGTGTCCATATTCTTAATTGGAGTTGGGGACATCCAGCAGGAGCTTCTTCTCCGCATCTCTGGCTCTGAGGATCACATGATCACCGTGCCTTCATACGATGACCTAAAATACTCAGAGGATGTGCTGGTACAGATGGTGTGTTCAGGTAAATCA
Associated Phenotype:
Not determined