ZMP
vwc2
Ensembl ID:
ZFIN ID:
Description:
von Willebrand factor C domain containing 2 [Source:RefSeq peptide;Acc:NP_001108100]
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 |
---|---|---|---|
sa30970 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa30970
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110237 | Nonsense | 248 | 309 | 2 | 3 |
ENSDART00000147868 | Nonsense | 248 | 309 | 3 | 4 |
Genomic Location (Zv9):
Chromosome 13 (position 16229799)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 16049834 |
GRCz11 | 13 | 16180826 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTATGTTCAGTGTCAGCTTGCCCACAGACAGAGTGTGTTGATCCGGAGTA[T/G]GAGCCTGACCAGTGCTGTCCAGTGTGTAAGAGCGGTAAGTGTTCGTGTTT
Long Flanking Sequence:
CCACAGCGATTAAAAGACACAACATCAAGTCATGTAGTTTGAACGGCACAGTGATCTGCCAATGTTTAAAGTCATGTAGGATGAACAAGGCTTGGTGATAGTGAAATCAATGAAGATTGGCCAACAGACTGGTCAAATTTAACCATGAAACTTCCAAAACTAAGTTGGCCAGTGTTTTATTTTCATTGTCCAACCTCTTTACAAACAGTACCATGCAGTAATTGTGTCTACGCACACATAAATGAAACGTTTGAATACTTTTAGTTTTATGACATTCCTTTAACAAATCGGGGGTGGAAAGTGTGAATAAAAATAGTTCCTTGAGACAGATAATTCCCTTTAGTTAAAGCACCACATATCGATCCTAATAATACAATGAATACATTTTTTGGTTTGTTCTTCTAGGTGTCTCCATGTGAGAAATGCCGTTGCGAGCCCAGTGGGGAGGTGCTATGTTCAGTGTCAGCTTGCCCACAGACAGAGTGTGTTGATCCGGAGTA[T/G]GAGCCTGACCAGTGCTGTCCAGTGTGTAAGAGCGGTAAGTGTTCGTGTTTCTCCAGACTTTCTGTCGAACTGCAGAACCCCCGCTATGTCCCCTAGGAGGGAAAGAGGTGGGTTAGAATTACTTGTGTAAAATGACCACTGAGACTTCAGTCCACTACACCCAATTACCAAACCGTGGAGAACATTCACAGAAAGCGTGCACAGAACTGTCCGCCTCTCCTATGCCTTGCGTGTGCATCCATCTCATTGTTCTATAATAGCCCGTTTACCATCAGTAAGATGATGCAAACCCAAGGAGAGTGCATTTGTCTGCAGGCCTTTGTTTAGGATGCATTATTCAGACAGCAATAGCATTAATGAACCTGCAAAGTTGCTCTGCTTGTTTCCAGGAGGTGAGGTGATTAGCACAGGCAGGTGTTTCGACTGCAGTCTGCTTTCTCCTGCCCTAGGGCACAGATGATTAAACTTTTACACATGTTTTTTTTCTCCATTTGGCTGGA
Associated Phenotype:
Not determined