Busch Lab

ZMP

vwf

Ensembl ID:
ENSDARG00000077231
ZFIN ID:
ZDB-GENE-070103-1
Human Orthologue:
VWF
Human Description:
von Willebrand factor [Source:HGNC Symbol;Acc:12726]
Mouse Orthologue:
Vwf
Mouse Description:
Von Willebrand factor homolog Gene [Source:MGI Symbol;Acc:MGI:98941]

Alleles

There are 10 alleles of this gene:

Allele Name Consequence Status Availability
sa10088 Nonsense Available for shipment Available now
sa10698 Nonsense Available for shipment Available now
sa32187 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa10088
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
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Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000114690 Nonsense 468 2812 11 51
ENSDART00000134872 Nonsense 454 2059 10 34
ENSDART00000142905 None None 444 None 11

The following transcripts of ENSDARG00000077231 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 18 (position 6250602)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 7205703
GRCz11 18 7164665
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAAACAYGGGGGAGTGGTCTCTGTTGATGGAATGGATGTGCAAACACCCT[T/A]AATTAATGGTTTGTCAASATGYAATAATGCATACATAATTCACACTGCTG
Long Flanking Sequence:
ATTTATTAGGCTCTTCACGTTTGAGTTGAGATTACGTTAAACTTTGAATTGAAAATTGACATTTCTAACAACTTCATGGGAACTTTGGGGGGGGGGGGGGAGTAATATTTTAAATAAAAAATTCTGATTCATTTTGTCCTCTTTCTATCTATAGGTGAGTGTTTGGTGACAGGACAGTCGCATTATAAGACCTTTGACAACAAATTCTTCACCTTCAGTGGGATTTGTCACTATCTGCTTGCTAAAGACTGCCAGAGCAACTCTTTTTCTGCCGTCATTGAGACTGCACAGGTCAGTTTCTTTCATCACACTGTCGTATTTGTTTTTTGGTAGTTTGGTTGTGCTTATGTTTGTGCATCCCTGTACAAAGTGTGCTGATGATCAAGATGCCATCTGCACACGCTCAATAACACTGAGGTTCAAGGATCTGGCCAATCAGACGGTTCACCTTAAACATGGGGGAGTGGTCTCTGTTGATGGAATGGATGTGCAAACACCCT[T/A]AATTAATGGTTTGTCAACATGCAATAATGCATACATAATTCACACTGCTGAATTATTTAGATGTTATGTAATGAGAATAAGTGTTTGTGTGTTTGTAGGTCCCCTGAGAATCCAGAATACCGTGTTGTCATCTGTGAGACTGCGTTATGGACATGATTTACATCTGGATTGGGACGGCAGAGGACGTGTTTTGCTCAGGGTAAATGTGGCCTGTTAAAAAAACAGGCTTTGGAAGCTTAACTCGGTCAAGTTTAAGGGGTTAGTTCACCAAGAAATGAAAATGACCTCATTATTTAATCTCCATTGTGTAGTTTTTAAAACCTTTTTCTGGTCTCTTTCTGCTGTTAAGCACAAAATAAGATATTTTGAAGAATGCTGGTTTCTGGCACCCACTGACCTTCATTGTAGGACACAAAATATTTTGTAAGCCAGCAACCAGCAACATTCTTCATAATGTGTTTAACAGAAGAAAGAAACTCAAATAGGTTTCGAATAAGGGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10698
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000114690 Nonsense 597 2812 14 51
ENSDART00000134872 Nonsense 583 2059 13 34
ENSDART00000142905 None None 444 None 11
ENSDART00000114690 Nonsense 597 2812 14 51
ENSDART00000134872 Nonsense 583 2059 13 34
ENSDART00000142905 None None 444 None 11

The following transcripts of ENSDARG00000077231 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 18 (position 6253836)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 7208937
GRCz11 18 7167899
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCTCCATGAAGTTCGAACCCTGTCATKATATGGTGAACCCTGAGCCGTA[T/A]GTGAAGAACTGCCGCTATGATGTGTGCGCATGCGCAGATGGTCAGGAGTG
Long Flanking Sequence:
ACCATTTTAAGGTCAAAAATATTAGCCCCCTTAAGCAATTTCTTTTTTGATTGTTTACAGAACATCTATCATACAATAACTTGCCTAATTACCCTAACTTGCCTAGCTAACCTACTTTAATTAACCTTGTTATGTCTTTATTCTCAATACTAGAATCTTGAAAAATATCTAGTGAAATATTATTCACTGTCATCATGGCAAAGATAAAAGAAATTATTAAAACTATAATGTTAAGCATTAAGATTAAACAGTTAATGTTAAACAGAAATTAAGTTAAAAAAAATTCAGGAGGGCTAATAATTCTGACTTTAACTGTATGTGTATATAATGCAATGTACTGTTTACATATGCACTAAACACTAGAGGGCAACAAAGACCAGCAGGAAAGATTTTAATGTTTTGGTATGTGTGTCTGCAGTGCGTTTTGCAGAAGAGGCCTGTGCTGTGCTGCTCTCCATGAAGTTCGAACCCTGTCATTATATGGTGAACCCTGAGCCGTA[T/A]GTGAAGAACTGCCGCTATGATGTGTGCGCATGCGCAGATGGTCAGGAGTGTCTGTGTGACGCTGTGAGCAGTTATGCAGTCGCGTGCGCAGCCAGAGGAGTGCTGGTCAACTGGAGGAGTCACGGATACTGTGGTATATATGCTGTATATACTGTAAATATAGAGATTTGGGGTTCATAACTAATAACTGTATTTCGAGTCAGATATGTAAAAAACATCCAAACAAATACTTTAATTTTGTCTTATCACACTTTATTTAATAAAGGTAACGTTACTGTATGTCGCAGTTCCTCCAAGATTTAGCTATAAATTATTATTTGTTTGCTGTGGCTTTTCTTATAATCTGTGGTAATATTCAGGCCATTCGTGTAATTTTGCTGTGGAAATGTACGCAAATTTGTACTTCTTTTTTCTTTACGTTTCAACCAATGATCTCTGTAACTGACGTAAAGGAAACGCGGAGAGAAACAAACTTGAGTGTTTACCTTTTAACATATAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa32187
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000114690 Essential Splice Site 2488 2812 None 51
ENSDART00000134872 None None 2059 None 34
ENSDART00000142905 Essential Splice Site 272 444 None 11

The following transcripts of ENSDARG00000077231 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 18 (position 6299435)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 7254536
GRCz11 18 7213498
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCACATCGCTCAGTGTGTGGACCCCGTCTGCAACCAGATCTGCCCTGTGG[T/C]GCGTCCTACACAACTCCGCCTCAGTCTGTGAGATTGAGTCATATTCACTT
Long Flanking Sequence:
GTCTCTTCCCCTGCCCTTTCTCAGTGTGCAAAAAGGATCAGTGTCCTGACTCAACAAAACCTTCCTGTCCTGCATACAAGAAGCTGTCGGTGAAAGCATCCGAGTGCTGCGATTCATACCAATGTCTGTGCAATTGTCAAAACATCACCCGCACCTGCCCTCCAGGCTACATCACAAAGACCAGCACCAATGATTGCCAATGCACAGAGGTCACCTGCACGCCTGATAAGGTTGGCACGCTTTAAAAGTCTCGCTGAGTGTGTGTATGTGTGTGTGTTATTGACTTGCCCTTGCAGCGCTGTGTTTTGGACTCTGAGATCAGCATGTGACGGGTTATTTATGTGTGCAGGTGTGTGTGGTGGACGCTGTGGTGTACCAGGTGGGCAGCAGGTGGGAGGAGAAGTGTAAAACTTGCAGATGCACCGAGCAGACGGACGGACAGACCGGCCTGCACATCGCTCAGTGTGTGGACCCCGTCTGCAACCAGATCTGCCCTGTGG[T/C]GCGTCCTACACAACTCCGCCTCAGTCTGTGAGATTGAGTCATATTCACTTGGGAAGTTTTAAATTTTTTTATTTATAGAAGTTTTTACAACCCCAAATCAGAAAAAAATTGGGACCGTTTGGAAAGTGTAAATAAATAAAAAAATGTGATTTCCAAATTGACTTATTTGACAATTGACTTGACAAAATACAAAATATTTAATAATAATAATAATAATATTAATAATAATAATAATAATAATAATAATAATAATAATAGAGCATTTTAAAGCTCTATGTATTTATTTTTTAATGAAATTTTACAGATCTAATTAACTTTCAGATAATTGTTTAGAAAAACAATATATTTCTTTATATATAATATCTCTCCTACAATATATGTCTAGACTACAAAAATGTCATTAAAAATCACTTTGTTAAACAATATGGTTAAATTTCCTATTAAAATACAATTCATAATATAAACAGAAAACACCCTTGAGTCATGAGCTAAAGACAACA
Associated Phenotype:
Not determined