ZMP
wu:fj80h11
Ensembl ID:
ZFIN ID:
Description:
Wu:fj80h11 protein [Source:UniProtKB/TrEMBL;Acc:Q7SXB9]
Alleles
There are 6 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa22948 | Nonsense | Available for shipment | Available now |
| sa22947 | Nonsense | Available for shipment | Available now |
| sa42819 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa25031 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa36255 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa16938 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa22948
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000032188 | Nonsense | 110 | 692 | 1 | 12 |
Genomic Location (Zv9):
Chromosome 16 (position 50592121)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 47446196 |
| GRCz11 | 16 | 47381282 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATTTCAGGTGCACACTCTGGACGGAATGTTTGTTTACAGTCCTCGGAAT[G/T]AGTCAGGGCGCGCGCTCATCGTGCACGCGTTCACCAATAAATCCGCTTTC
Long Flanking Sequence:
CCGAATAGTAGGAATGATCAATGTATAATTCAATTTCTTATTTTGCATGGTAATACGCTTATAACGCTTTCCTATTGGCCACCAGAACATGTCACTCAAACCTGCCAGGCCTCCGTAGGTCACGCCCCCGCGTTTATCCAAAACTATAAAAGTGAAACAATGTAGGAAAACTCGATTTCCTCATCGGACGCGTCCACAAACAGCGTTATACTTCACACGCCACGTGTTCACGAACAAAGAAATGCACATTTGCATCTGAAACCATGTTTTATTGTCGATTTCTGCTTTATTTTTATCTGCTGTATTTCGGCGCGTCGTTTCGCGTTATAGCCGCGTCTTCTCAAGGAAACGACAAAGCGCCGAAAAATCTACATTTAGTGAAGCGAAACGCAATTAAAACCAGGCCCAGCGATGCTCTTGGAGGGCTTGAACCCGGTGATCCCGCTCCTGCATTTCAGGTGCACACTCTGGACGGAATGTTTGTTTACAGTCCTCGGAAT[G/T]AGTCAGGGCGCGCGCTCATCGTGCACGCGTTCACCAATAAATCCGCTTTCCTCGAGTGTTTGTGGACGTGGAGCGAGTCTCTGTCGGACCTGCTGGATTACCTGCCGTCCAGCACTGAAGTTTTAATGCTGTCCATGGATGAGACTGCTGAACAGGACGCCCTCTGGATGAGGGAACAGGTGTACAGAGCCGCTGCTCACAGGTACTGACAATGCAGACCTGAGCACTTTCAGTACAGTACCCCTCCGCTCTGTTACCTTCTGATTGTTGAGTTAAAGTAATATATTGCTGTTTCAGTCTTACAATAGACAAAACAAAAGAAAGATTACCCTAAGGCTAACACTTTCACATTCCTTAGTTACTTTTTTCCCCCAACACTGTCCTTGCTGTATGTGGACCTGTGTCTGAAAAGTTCACTTCAAAGTTAGATAACAGGTACTGACATTTTGGACCTGATATCATTCAGCCCTACATTACCACCTCCACAGTATTACCTTGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22947
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:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000032188 | Nonsense | 169 | 692 | 1 | 12 |
Genomic Location (Zv9):
Chromosome 16 (position 50591944)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 47446019 |
| GRCz11 | 16 | 47381105 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCTGTCCATGGATGAGACTGCTGAACAGGACGCCCTCTGGATGAGGGAA[C/T]AGGTGTACAGAGCCGCTGCTCACAGGTACTGACAATGCAGACCTGAGCAC
Long Flanking Sequence:
TCCTCATCGGACGCGTCCACAAACAGCGTTATACTTCACACGCCACGTGTTCACGAACAAAGAAATGCACATTTGCATCTGAAACCATGTTTTATTGTCGATTTCTGCTTTATTTTTATCTGCTGTATTTCGGCGCGTCGTTTCGCGTTATAGCCGCGTCTTCTCAAGGAAACGACAAAGCGCCGAAAAATCTACATTTAGTGAAGCGAAACGCAATTAAAACCAGGCCCAGCGATGCTCTTGGAGGGCTTGAACCCGGTGATCCCGCTCCTGCATTTCAGGTGCACACTCTGGACGGAATGTTTGTTTACAGTCCTCGGAATGAGTCAGGGCGCGCGCTCATCGTGCACGCGTTCACCAATAAATCCGCTTTCCTCGAGTGTTTGTGGACGTGGAGCGAGTCTCTGTCGGACCTGCTGGATTACCTGCCGTCCAGCACTGAAGTTTTAATGCTGTCCATGGATGAGACTGCTGAACAGGACGCCCTCTGGATGAGGGAA[C/T]AGGTGTACAGAGCCGCTGCTCACAGGTACTGACAATGCAGACCTGAGCACTTTCAGTACAGTACCCCTCCGCTCTGTTACCTTCTGATTGTTGAGTTAAAGTAATATATTGCTGTTTCAGTCTTACAATAGACAAAACAAAAGAAAGATTACCCTAAGGCTAACACTTTCACATTCCTTAGTTACTTTTTTCCCCCAACACTGTCCTTGCTGTATGTGGACCTGTGTCTGAAAAGTTCACTTCAAAGTTAGATAACAGGTACTGACATTTTGGACCTGATATCATTCAGCCCTACATTACCACCTCCACAGTATTACCTTGTGATTCATTCCACTCTGCTACCAGTGTTGGGTAAAAAAAGAAAATCCATCCATCCATATCGTTTTGTCATTTCAGTCGTTACGTCCCACCCTCATTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTGTCTATCTATCTATCTATCTATCTATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42819
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 |
|---|---|---|---|---|---|
| ENSDART00000032188 | Essential Splice Site | 282 | 692 | 3 | 12 |
Genomic Location (Zv9):
Chromosome 16 (position 50587431)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 47441506 |
| GRCz11 | 16 | 47376592 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGGAGCTGTCGCTTGGGTATCAGAGGGAGGATGCTCTTTCTTTACTAAG[G/T]TGAATTACATGAGCTAAACAACGTGGATTTTGGTTCAATATTTAAGAAAT
Long Flanking Sequence:
CAGACCTGAGTGAGAAGCAGCCTTCTGCCATTCCAGGTTTGAATCTGCTGGATATATCAACGTATATGTAGCTCCACCTTCTTTTAAAAAGAGGTCTGGGTGCACAATCTCATCAGAACTTAAAGCAACAGTCCTTAAAATGGCAGAACTTGGATCGAAGCCTAAAAGGGGCAGTATTTAAAGAGTTATAAAAATAATTATTTATTTGATAATTTAAGGTGAAACGTCACGTACACACTCTAGGGACCATCAGAGACTTATTTTAAGTAAAAGTGGGCATAATAGGTCATTCCAGTTTTGTATCTGTGTATTCTGTAATTGCAGACTGGAAGGGGCCTGTGATCGGCAAGCGTCTGAATGCCCGATATGACTGGCTGTACGCCCACTGGAGTACAGATCCATACAGACTGCTGGATGTTGGCGATGGATGTGCACCTGTGGCTTCTCTCAAAGGAGCTGTCGCTTGGGTATCAGAGGGAGGATGCTCTTTCTTTACTAAG[G/T]TGAATTACATGAGCTAAACAACGTGGATTTTGGTTCAATATTTAAGAAATGGACTGATAATTGTGTTTTATGTTTAAGATTAAAAACATGGAGAAGTCAAACGCTACCGGGGTGTTGGTGTATGCCTTGCCTGGAAATAACATTCAGGACATGAACTGCAAAGGGGATGAATGTTTTACTTCACTCCATATACCTGCATCGATGGTTCATTTCCAACCCAAAGTCAAAGAAGCCCTACAGTGAGCAAACCGATTATAGCTCCTGACTATGGGGAGAAAAATATGGACGTGTTTTTGTGTCACATCTTCATTTAGGTTAATGTACAGTGCTCGGTGTATTTTTATCCATTTTCTCAGTGAAAATAGGCAATGTGTTTTGGTGCATTTAAACAAAACTGATTTATTAAAGATATATTTATTGAAATAATATTTTAGTCACCAAACCTATTGATAAATTGAAATATAATACAATTAAATTCGAGCAAAATATTGCAAAAAATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25031
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000032188 | Nonsense | 314 | 692 | 4 | 12 |
Genomic Location (Zv9):
Chromosome 16 (position 50587257)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 47441332 |
| GRCz11 | 16 | 47376418 |
KASP Assay ID:
554-7441.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCTTGCCTGGAAATAACATTCAGGACATGAACTGCAAAGGGGATGAATG[T/A]TTTACTTCACTCCATATACCTGCATCGATGGTTCATTTCCAACCCAAAGT
Long Flanking Sequence:
TATTTAAAGAGTTATAAAAATAATTATTTATTTGATAATTTAAGGTGAAACGTCACGTACACACTCTAGGGACCATCAGAGACTTATTTTAAGTAAAAGTGGGCATAATAGGTCATTCCAGTTTTGTATCTGTGTATTCTGTAATTGCAGACTGGAAGGGGCCTGTGATCGGCAAGCGTCTGAATGCCCGATATGACTGGCTGTACGCCCACTGGAGTACAGATCCATACAGACTGCTGGATGTTGGCGATGGATGTGCACCTGTGGCTTCTCTCAAAGGAGCTGTCGCTTGGGTATCAGAGGGAGGATGCTCTTTCTTTACTAAGGTGAATTACATGAGCTAAACAACGTGGATTTTGGTTCAATATTTAAGAAATGGACTGATAATTGTGTTTTATGTTTAAGATTAAAAACATGGAGAAGTCAAACGCTACCGGGGTGTTGGTGTATGCCTTGCCTGGAAATAACATTCAGGACATGAACTGCAAAGGGGATGAATG[T/A]TTTACTTCACTCCATATACCTGCATCGATGGTTCATTTCCAACCCAAAGTCAAAGAAGCCCTACAGTGAGCAAACCGATTATAGCTCCTGACTATGGGGAGAAAAATATGGACGTGTTTTTGTGTCACATCTTCATTTAGGTTAATGTACAGTGCTCGGTGTATTTTTATCCATTTTCTCAGTGAAAATAGGCAATGTGTTTTGGTGCATTTAAACAAAACTGATTTATTAAAGATATATTTATTGAAATAATATTTTAGTCACCAAACCTATTGATAAATTGAAATATAATACAATTAAATTCGAGCAAAATATTGCAAAAAATTACAAAATGCAAAATTTCAGCAAATTTTTTTTTTTTTTAATTTTTTTTTGCTTTATTGCATTTAATATTTTTATATTGCATATACATTTATCTATACTAGTTTTTGAACCGTTATTATTATTTTTTTTTTGATAAGCTCCAGATTTAGCTTCAAAACTGACTAATATCCTGTATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36255
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:
A > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000032188 | Essential Splice Site | 480 | 692 | 8 | 12 |
Genomic Location (Zv9):
Chromosome 16 (position 50580822)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 47434897 |
| GRCz11 | 16 | 47369983 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGAGCGGGGCATTATTCAGTGCACTGAAAGTGTTTCTGACTGTGTTTGC[A/C]GAGGCACAGGCCATTGGCTGACAGACGTGTCTGCTTTGATTCCCCTGCTG
Long Flanking Sequence:
ATCTATATAAAATGCTGCGCTTCCCACCTCCTTTATTCAGCCGCAATGACTTCTCAACTGAGTTTTGCGTTTAAGTTTGCATCGATGCGTCTTCAATATCAAGAACACATCTGGGAACTTTCACACATCCTCCATTTTTGTGGTCCTTGCAGTACTGGAACTGAGCTTTGGCACTTGATGTTACATGAGAGCACAAGGGCGCAAGATTGCTTAAGAACGCATATTAAGAAACAGACTGGAAGACTGAAAGACCTGTAATGGATGTGACAAAGGAAACATTCAAAACATGCTGTGCTGGTTGTCCTCCAGGAACGTGGTTGAGAAACACTGCTCTAGGGGACTTGTAAAATAAGCCAATTTACAAAAAAAAACAACCATATCTAGTGTGTGAGTACACCCTAAATGTTTAATTCTTGGATTGACCATCCCTTTTAAATTCTCATTCAGGTTGAGAGCGGGGCATTATTCAGTGCACTGAAAGTGTTTCTGACTGTGTTTGC[A/C]GAGGCACAGGCCATTGGCTGACAGACGTGTCTGCTTTGATTCCCCTGCTGAATAACAAGAAATGCTCCTTCACCATGAAGACTGCGCCATGGGCAATGCCATGGATGACTACTCTCAATCTGCGCTTCAGTCAGAGCAATAAGACAGGTCAGAATCAGAATGCAAACATGATAAAACATTTAACCCTTGTGAGCTGTTGGGGATGTTTTCATCCACTCTGAGTTGATTTATTGTCTTAATTCAGCCACAATGTTCTCTGTGTTTCAGTAAATGGAATGACTTTTGCTGCCAAATCTTATCTTGACGCTTATTTTGGGCTTTAAAAATTTGCAATAACTCAACAGTACACTCTGGGCACCCTTTTGTTATGTTGGTGGCTGTTTTTGCCCCATTGACTTCCTTTTATAATTACATTTTTGATTGCAAAGCCATGACACCATATAATCATGCATTCTTGATTACTGCTGGTTTTCCCTGTTGGGAAGAGGTCAAATTTGTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16938
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000032188 | Essential Splice Site | 566 | 692 | 9 | 12 |
Genomic Location (Zv9):
Chromosome 16 (position 50577974)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 47432049 |
| GRCz11 | 16 | 47367135 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCGCAGATACCATGAGATCACCTTTAGTATTCCAGCTGCAACAAAGAAGG[T/C]GATGGATCCTCGTATAATATTATTGTAATGTATACATACAATAAAACTTA
Long Flanking Sequence:
CTGCATTTATTAAAAAAAGCAGGAAGTGTTTATATCATCTGCTGAAAATATTATATTAGTCAGATTACACTTCTGCCTTAATCAGGTGCTGTAAAGAACAGCTGTTATTCAGCTTCCTGTGCACTCACAGATTGCAGTCAGTGTCGCTATTTTATGATTTAAGCTTCTTTAAACAAAGTCATACTGATGATTATCATTTGCTTTATTTTTAGTGCACTTGTAGGAAACCATAAGTTCATTCTTGGAAGCTACATTTTAGGGGTTTGGCTGTGTGAATGTGTCAGTATGATTCTAGCTGATGTAGTAATAAAGCAAGTTAAACGGATCTGCTGTGGGATCAGAACATGTGTCATGAATATTGACGACCTCGGGCACTGTGTTTGCAGAAAGACTGTACCCTTTCGAGGTGATGCCGCTGTTCAATGGAGGGACGTTTGATAAGGACTATAACCGCAGATACCATGAGATCACCTTTAGTATTCCAGCTGCAACAAAGAAGG[T/C]GATGGATCCTCGTATAATATTATTGTAATGTATACATACAATAAAACTTACACTATATTCAGTCAAGGCCGAAATTGTTCATACCCCTGGCAATCTCTGACTTGGTTACTTTTTGTTCATATTTTATTCAGCAATGTTTAATAATTTATTTTTAGTACTGGATATGGCATCTCGCAAAAGACCATATGCACATGTTACATTTGAACATAAAGCGACATGTGCAAAACTATTCATACCCTTCTCAATGATTAATAAAGCTTTTATTGGCTGTTACAGCAATCAGACTCTTCCTACCATTTCTGACCTGAGTTTTGCATTCCTCTGCTGGTATTTTTACCCATTCATCTCTGGTTGGATGGTCTACTTCCCATCACCCTGATGTTTAGCTCCCCCCACAGTTTCTTAATTGGTTTTAGGTCAGGACTCTGGCTGGGTCACTGCAAAACATTAATGTTTCTGTATACAGTCAAACCTGAAATTATTCATGACACTGGCAAATT
Associated Phenotype:
Not determined