ZMP
vwc2l
Ensembl ID:
ZFIN ID:
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 |
---|---|---|---|
sa16824 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa16824
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 |
---|---|---|---|---|---|
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)
KASP Sequence:
ACTTCTGTGAWTACAGAGGGAAGACGTATAARATCCTGGAGGAGTTCAAG[G/A]TAGGAACACGCTGTCTGTCRAATTTTTATTATGTGCGGGTATTRAACTGT
Long Flanking Sequence:
GCTTCGGATTGTTTACATTTCTTTCAGTGTCATATTTGCAGCATGGAGCCTTACAATTTAAGGGATCTGAGACACTCTCCTTGAATGCGTCAAGACAGCCGCGGCGAAGGATGGGCCCTTTTCTCCCGGCGATTTGCGTCGTGCTGCTCGCCCTGAACGCCGCTGTCTCGCCGGCCTCTGTCGGCCCTGAGGACTATCCCGCCGCGGACGAGGCCGAGAGAACTGCCAACAATGACATCATTTTCGATGACTACCGAGGGAAAGGCTGCGTGGATGACAGTGGCTTCGTGTACAAGCTCGGGGAACGCTTCTTCCCGGGCCACTCGAACTGCCCGTGCGTGTGCACGGAGGACGGACCGGTCTGTGACCAACCCGAGTGCCCTAAAATACACCCCAAGTGCACCAAGGTGGAACACAACGGTTGTTGCCCCGAATGCAAGGAGGTCAAAAACTTCTGTGAATACAGAGGGAAGACGTATAAAATCCTGGAGGAGTTCAAG[G/A]TAGGAACACGCTGTCTGTCGAATTTTTATTATGTGCGGGTATTGAACTGTTTAACATACACGTCTCATTCCAGTCAAAACTTGAATTCAACCTTATAGGAGAATTAATGTTTATAAATTACCCAAATGGAAAAAGCTTCTCGTTTTTGATGAATTCAGGTGGATTTATACAGTTTCAACTGATAGATCATGTTCAAGTTTCACTATTATGCCTCAGGGCTCTTAACATACAGTAGTCACTAAAAGGGGTTTTTACAGCAAATGCCATACCATTTATTATTTTATTCCCTGAGGCATAAAACGTTAGAATTAACAGTTTATAAAGGGATAGTTTACTGTAAAATTAAAATTCAATCATCATTTACTCACTCTTGACTTTTTCCCCACTGTAAAACATGTTAAATCAGTACAACAACAACAAAAATAATCCTTATTTCCTTTTTTTTTTTTTTTTTTTTTTTTTGTTTATTCAACTTTTAAAACACATCAGCTGCTCTGACC
Associated Phenotype:
Not determined