Busch Lab

ZMP

si:ch211-246m6.5

Ensembl ID:
ENSDARG00000011673
ZFIN ID:
ZDB-GENE-050208-577
Description:
Novel protein containing EGF-like domains [Source:UniProtKB/TrEMBL;Acc:B0V3W1]
Human Orthologue:
VWDE
Human Description:
von Willebrand factor D and EGF domains [Source:HGNC Symbol;Acc:21897]

Alleles

There are 6 alleles of this gene:

Allele Name Consequence Status Availability
sa12831 Nonsense Available for shipment Available now
sa16549 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa12831
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
ENSDART00000033332 Nonsense 712 1983 12 32
ENSDART00000133365 None None 255 None 9
Genomic Location (Zv9):
Chromosome 22 (position 14378347)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 14209254
GRCz11 22 14233829
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTTAANNNAGATGAAAGGTGCTAAACTGAAGTCTCAGTTGTCCAGTGGTT[T/A]GGCAGACAACTCTCTCTCTGTCAGGGAATTGGAATTGGACTCATTATYTA
Long Flanking Sequence:
CTTGATTTGCTCGTTTTAATGTCAAATATAATTAAAGCTGGGGAAAATCTCTAATCTAATGGGCTAACCTTTCTCGAACTCTAAATCCTCTCTTGACGCAGTGCTTGAGGGCTTAATTCAAAGGCTGATTTGAGACAGTCATATTTTTGTTTTATTTCTCCGTGTCAGGATCGCGCCTGGGGAGAGCCTGTTTGACAGCACGCCACCTGCCGTGGATGAGGAGATAAAGTGGAATTTCTGTGCTTGTCAAAAGGGATACAGCCTGTCCCTCCATTCAACACGCGCCTCAGAAGGCCTATTAAACCCACCTCCTGTCTCTCGCTGCCTATCTTACGACAACACAGATTACACGTCCCTGTTCCCCTTCAAAGACGCCACTGCTGAGTATGCTGTTAAACCCTTCTCCACCCGTAACGTCCAGAAGCGGGAGGCTTTGGCTAAAGCATCAGAGTTAACCAAGATGAAAGGTGCTAAACTGAAGTCTCAGTTGTCCAGTGGTT[T/A]GGCAGACAACTCTCTCTCTGTCAGGGAATTGGAATTGGACTCATTATTTAAAGTTCACAATCCTCACTTGAATGAATCTAAGGTACCCTCACCAAGGCTAAAGAGACAAACCCTTGACTTTCAGCCTGTTTACACCTTCCAGGCTCTAAGCCAGACTGACCTCGAAAGTTTCGCCTACTTCTTTCCAGATGACCACCGCTCTTCCAGCCGTCCAGCTGCCCACCCTTCCTGGCCGACACCTAGCGGTCTCACTTCTGCCAAAGCTTTGGAGGTCTGCCAATCGACCTTGGCCAACTCAACCGTGGGCACGGTATGTAAGAGTCTGCTGGGTCGGCGCCTGGAAGAAGCTGTGGATCTCTGCATCCTGGATCTTCAGTTGAAAGATGATTTGGCTTGGGAGGACGCACTCGTGCCCTTCCTGGAAAACGAATGTGAGCGAAAATGGCTGGAGAACCGGAGCCAGAGTTCTCAAGAAGCTTCCAAATCTTTGGCAGATATTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16549
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
ENSDART00000033332 Nonsense 1624 1983 22 32
ENSDART00000133365 None None 255 None 9
Genomic Location (Zv9):
Chromosome 22 (position 14307724)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 14138732
GRCz11 22 14163509
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCCCCAGGAGAGSTTCACCTACCTTGGTGAACAAAGCCACACCAAGTCTT[T/A]GAGCAACCAACCAGMTCTTGAGAAAGGTAGACACCCAAGCAAAACCAGCA
Long Flanking Sequence:
TCACCATCAGGCTACCACTCGCATACCCCTCCCGCCAACATTTCCACCTGTCACAGAGAAAAGAAAGTTGGCGCTGACGACAGGACGCATGCCGGCCTCAACTAGCGGAAGGGATCAACTTCTTTCTGGCTCTCACAATCAACTCAATGTTCTCCCGAGTCCCACGGATCGAGATGCTTCAGTTAAAGTCTTGACAGGTGGATTTGCGGGTGTCACATCTGGAAAAGTCACTTTACCTCACACTTCAAGGCATGTTGAGGCACTGAGGCAGACTCAAAAACAATCTAGTCCGGCCACAATTTCCCAAGCTCGACCTTGGACTCCTCCAGACACCCAGCGACCCCTAACAGCAGCTTTAACCTCCCTCTCCTTCTCCTTCTCTGAGTCGGAGTTCTCCGCAGATGGAGGCCTTGGAGCTGGAATTCAAGACCCTTATGAGTCCCAGCCACTTCCCCAGGAGAGCTTCACCTACCTTGGTGAACAAAGCCACACCAAGTCTT[T/A]GAGCAACCAACCAGCTCTTGAGAAAGGTAGACACCCAAGCAAAACCAGCAACGTGGTTCTCTTAGAGGAGAGAAGTTTCTCCTGTGCAGATGTTTCTTGCTTCCCTGGAGTACACTGTGAGCTTGCAGGGGATGGACAATCTAGATGTGGACGGTGTCCTTTGGGGTACACCGGAAATGGACAAATGTGCAGAGGTAATTCTAGATGTATAGATGTCTTTTCTTCATTAATCATTTAGTCCAACAGTTAGTGACTTGCTTATCTATGACACAATTTTTTTGTATTGCCTACTTTAAACACATATGTACCCTGCTGACCCCAGAAAGTGTGTAATAGTACCTTAAAATACAGGTATCTAACCTTAAGGTGTTGCTGAATAAATTTTAGACATACACTAGTCCAGGAGTTCTCAAAATCGGTCCTGGAGGGTTGGTGTCCTGCAGATTTTAGCTCCAACATGCCTCAACACACCTGGAAGGATGTTTCTAGAAATCCCAGTA
Associated Phenotype:
Not determined