vwc2l

Ensembl ID:
ENSDARG00000069134
ZFIN ID:
ZDB-GENE-081104-169
Description:
von Willebrand factor C domain-containing protein 2-like [Source:UniProtKB/Swiss-Prot;Acc:B0UZC8]
Human Orthologue:
VWC2L
Human Description:
von Willebrand factor C domain-containing protein 2-like [Source:HGNC Symbol;Acc:37203]
Mouse Orthologue:
Vwc2l
Mouse Description:
von Willebrand factor C domain-containing protein 2-like Gene [Source:MGI Symbol;Acc:MGI:2444069]

Alleles

There is 1 allele of this gene:

Allele name Consequence Status Availability Estimate
sa16824 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa16824
Current 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:
G > A
Consequence:
Essential Splice Site
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000100394 Essential Splice Site 130 223 1 3
ENSDART00000132911 Essential Splice Site 130 223 2 4
Genomic Location (Zv9):
Chromosome 9 (position 41621752)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 40746922
GRCz11 9 40548709
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
ACTTCTGTGAWTACAGAGGGAAGACGTATAARATCCTGGAGGAGTTCAAG[G/A]TAGGAACACGCTGTCTGTCRAATTTTTATTATGTGCGGGTATTRAACTGT
Associated Phenotype:
Not determined

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