ZMP
si:ch211-246m6.5
Ensembl ID:
ZFIN ID:
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 |
sa43797 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa43796 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa16549 | Nonsense | Available for shipment | Available now |
sa958 | Essential Splice Site | F2 line generated | Not yet available |
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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:
sa43797
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:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000033332 | Essential Splice Site | 1015 | 1983 | 15 | 32 |
ENSDART00000133365 | None | None | 255 | None | 9 |
Genomic Location (Zv9):
Chromosome 22 (position 14359551)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 14190559 |
GRCz11 | 22 | 14215134 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCATTCACACAGCATTAGTATCTAAACCTAATCTCTCTTTTTCTTCTTCA[G/T]GTGACTAATGATGGACAGCAGTACAGCGATGGCAAGATTTTAACCCTTTA
Long Flanking Sequence:
ATTATATGTGTCAGATGTCAGTTCAAAGTTTAGACTGACTATTAGCTAAATATAAATTTAACTTAAAAATTTCCTTGATTTGCTAAGACTCCACTGATCAACCTTCTGTATCACGAAGTAAGTGAATTTTTATGAACTAATTTCAAGAGGAGCATGTGATATGATTCGTTATCAGCAATAAACCAATCAGATTGATTCAAGCCTTTACTTAGTTTTAGAATTATCCCGACTTCCACCTCATCTCCTCCTTTTCCTCCTTTAGCAGGGGCAGCTCTCACCTGTGCCTGAGCTTAATTATTAATTGATGTCCTAGGCTCAATTATCTATAAGCTCAGGGGTTCTCTCCTGAAACAGCATGCCAAACCTGCTAATAGCGTCAAGCGAAATCTAAGTGTAAACTCTTTAAAAGCTAATTTAATGTTTGTGTTAAACATGTTTTAAAAATTATCATCATTCACACAGCATTAGTATCTAAACCTAATCTCTCTTTTTCTTCTTCA[G/T]GTGACTAATGATGGACAGCAGTACAGCGATGGCAAGATTTTAACCCTTTATGATGGTATTTGCCAGATATGTGTGGCTCCTTCTGGAATTTGTAAACTTAAGGTAATCATATACTCAAAGGCTTATGAGAAACAGAATTCATTTTTTATTTAGTGTACAGTTAGCATAGGGACAGTGAAAAATACAAAATGTCCACATAATTTTAAACATGTGGATTAAATAATTTTTTATTTTTTATTTGTTTAAAGACAGCAAAAAATAAATGAATATATACAAAACTTATTGGTATTTGGAGGTTTTAATAATTAGATTTGACATAAACATCAGAATCATTTCCATAAATGTTGTCTTTAATATAAAGTGTTTACGTTCATTTGTTTGATCCCACCGGTCTCCTGTGTGACCATAAAGGCAGTGTCTAATAGTATAATAATGCATAAATAAAACTTAAACAATAACATTTATTGTATAATGTATGAAATATTTGAATGCATTTCTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43796
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000033332 | Essential Splice Site | 1048 | 1983 | 15 | 32 |
ENSDART00000133365 | None | None | 255 | None | 9 |
Genomic Location (Zv9):
Chromosome 22 (position 14359447)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 14190455 |
GRCz11 | 22 | 14215030 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGTATTTGCCAGATATGTGTGGCTCCTTCTGGAATTTGTAAACTTAAGG[T/A]AATCATATACTCAAAGGCTTATGAGAAACAGAATTCATTTTTTATTTAGT
Long Flanking Sequence:
TCTGTATCACGAAGTAAGTGAATTTTTATGAACTAATTTCAAGAGGAGCATGTGATATGATTCGTTATCAGCAATAAACCAATCAGATTGATTCAAGCCTTTACTTAGTTTTAGAATTATCCCGACTTCCACCTCATCTCCTCCTTTTCCTCCTTTAGCAGGGGCAGCTCTCACCTGTGCCTGAGCTTAATTATTAATTGATGTCCTAGGCTCAATTATCTATAAGCTCAGGGGTTCTCTCCTGAAACAGCATGCCAAACCTGCTAATAGCGTCAAGCGAAATCTAAGTGTAAACTCTTTAAAAGCTAATTTAATGTTTGTGTTAAACATGTTTTAAAAATTATCATCATTCACACAGCATTAGTATCTAAACCTAATCTCTCTTTTTCTTCTTCAGGTGACTAATGATGGACAGCAGTACAGCGATGGCAAGATTTTAACCCTTTATGATGGTATTTGCCAGATATGTGTGGCTCCTTCTGGAATTTGTAAACTTAAGG[T/A]AATCATATACTCAAAGGCTTATGAGAAACAGAATTCATTTTTTATTTAGTGTACAGTTAGCATAGGGACAGTGAAAAATACAAAATGTCCACATAATTTTAAACATGTGGATTAAATAATTTTTTATTTTTTATTTGTTTAAAGACAGCAAAAAATAAATGAATATATACAAAACTTATTGGTATTTGGAGGTTTTAATAATTAGATTTGACATAAACATCAGAATCATTTCCATAAATGTTGTCTTTAATATAAAGTGTTTACGTTCATTTGTTTGATCCCACCGGTCTCCTGTGTGACCATAAAGGCAGTGTCTAATAGTATAATAATGCATAAATAAAACTTAAACAATAACATTTATTGTATAATGTATGAAATATTTGAATGCATTTCTTAAAATGGTTCATTATATATATATATATCCCAGACAGCACACATACGTTGGGCCGACGTCGGCCGAAGGTCAACACGTCGGCCCCTTTAATTCTAACATCGGTATA
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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
Mutation Details
Allele Name:
sa958
Status:
F2 line generated
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000033332 | Essential Splice Site | 1913 | 1983 | 30 | 32 |
ENSDART00000133365 | Essential Splice Site | 185 | 255 | 7 | 9 |
Genomic Location (Zv9):
Chromosome 22 (position 14292245)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 14123353 |
GRCz11 | 22 | 14148130 |
KASP Assay ID:
554-0863.1 (used for ordering genotyping assays)
KASP Sequence:
ATCCAGCTGTGTGGGAATTAAATAACAGTGTGCGTGTTTGTGTTTCTCCA[G/A]CGGTGTGTGTGCAGAAGTGTGTGAATGGTGGTGAGTGTGTGGGGCCGAAC
Long Flanking Sequence:
CCGAGAGTGCAAGCCTGAAGATGCAAGTGCAAGTTCTCAGTCTGGTACTAGTCAGGTGTACCTGATAAAGTGGCCGATGAGTGTAGTTCTTCCAGTCTCTTTTTGACTGTAGTTTAGTTCTAGCTCCCCCTGGTGTGAATGAATCCAGGGCTTTACCTTAGTATTTCTCTGCAGGTGTGTGTGAACCAGTGTGTGTGAACGGAGGACGCTGCATTGGACCAGATGTTTGTGACTGTGCATCGGGCTGGAGAGGAAAGAGATGTGATAAACGTGAGTAAAAAATAAAACAACCTGAAGTAAAGATGACAGTGACCTTTTGACCCCATGACAGCAAATGACCCCAAAGGTGTGAAATAAAGAACATCTCACAACAGAGAAGAAAAGTCGATCACAACTTGCACTAAAACCGACTATGAGCATAAACCTCAAAGTTAATATGTAAAATAACAGATCCAGCTGTGTGGGAATTAAATAACAGTGTGCGTGTTTGTGTTTCTCCA[G/A]CGGTGTGTGTGCAGAAGTGTGTGAATGGTGGTGAGTGTGTGGGGCCGAACAGCTGCCTCTGCAGTCCCGGCTGGAGAGGAACAATCTGCCAGATCCGTGAGTCTTTCCCAAAAACACAGATCCTCCAAACACACATTCCATGACCAGTCCAGACCCCAAATAAAGATATACATGCATGCAATTAATAACTCAAATTATGAACAAATGGTTAAATCATTAGTGTATGCCTTTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTCACTGTAAATAATTAATAATTGCATTTTTAGGATTTTAGTATTATTATTATTAATAAAACATTGTTTATAGTTTATATTTAAAGTATTACATATAAAATATATTTTACTATTTAAATTAAAACATATTTTTATATTTTTAAATGATATTCAATTT
Associated Phenotype:
Not determined