ZMP

LOC562406

Ensembl ID:

ENSDARG00000053460

Human Orthologue:

VWC2

Human Description:

von Willebrand factor C domain containing 2 [Source:HGNC Symbol;Acc:30200]

Mouse Orthologue:

Vwc2

Mouse Description:

von Willebrand factor C domain containing 2 Gene [Source:MGI Symbol;Acc:MGI:2442987]

Alleles

There is 1 allele of this gene:

Allele Name	Consequence	Status	Availability
sa9975	Essential Splice Site	Available for shipment	Available now

Mutation Details

Allele Name:

sa9975

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:

G > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000075499	Essential Splice Site	161	242	2	3

Genomic Location (Zv9):

Chromosome 3 (position 33570595)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	3	33304763
GRCz11	3	33436477

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TGTAAATCCTGTATACGAACCCAACCATTGCTGTCCGGTGTGCAAAAGTG[G/A]TAAGAGTTTACACATGCAACATCACATGTGCATTAACAATTTACCCAATT

Long Flanking Sequence:

CACATATAAAACAGTAAAAAAAAAGGAAAAAACAAATCAACATACATTAATAACGCAGATACAGCTAGACTAAACTTCCTGGAATGTGTTGAAGCAAGTTGGAGCTAAACTCAGCAGGGCATCAGCCCTAAGTAAAATAGCATGAATCTCACAAATTTGTTGGTTCTTTATATTTATACCTATACAAATCATAGCTTCCTAAATATTAAACAAACAAAAAATAGACAACTAAAAAAGTTTATATTTTTATGTCCTGCCATTATCTGAGAAATTCATGTTTTGCCTGTTCTGTCAATTAATTATAATAATAATAATATTAATGCCCTAATTGAATTCTGAAGTAATTAAAAGTAGTTCTTGTTTAAAACAGTTGTCACCCTGTGAGCGCTGCCGGTGTGAAGTCAACAAAGAAGTTTACTGCACCATATCCGGCTGTCCAGCTTTGCATTGTGTAAATCCTGTATACGAACCCAACCATTGCTGTCCGGTGTGCAAAAGTG[G/A]TAAGAGTTTACACATGCAACATCACATGTGCATTAACAATTTACCCAATTTTTTTCTAAACATAATCACATGCACCTTTTAAACTGTTGTGCAACTCTTGAGGATCAATGGAGTTACATTGGTTATTTCTTGTCTGTTGATTGATTTGTGCTCGATTACAGCATACTTCTGGGTGATGTCATGGAAAAAGAGTGATGCAACGGAACTGTTCGATAGATTGCGTACTACCATGCGGGGTATAAATAGGAACTAGATCGTGGCGTGCTGGGATGGCACAGGCACTATGGGGCATTGGGCCATCCCTGACAACAGAAGGCAAGAGCTGGACAGATTGCGTGTGATAAGTTTGTTCATGTAGAAATTAGAAAGTAATGTGTGGAGACTTCAAAGCATGCAGATTTTGGCTATGCATTTGTGCAGTCATTTTGGCAAATTTGCACATTTTGGTAAATCTAAGAAGTCGCCCTCTTAATTAAAAAGCCATTTAATTTTAGTTTTAT

Associated Phenotype:

Not determined