ZMP
wdr82
Ensembl ID:
ZFIN ID:
Description:
WD repeat-containing protein 82 [Source:UniProtKB/Swiss-Prot;Acc:Q6NV31]
Human Orthologue:
WDR82
Human Description:
WD repeat domain 82 [Source:HGNC Symbol;Acc:28826]
Mouse Orthologue:
Wdr82
Mouse Description:
WD repeat domain containing 82 Gene [Source:MGI Symbol;Acc:MGI:1924555]
Alleles
There are 6 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa1817 | Missense | Confirmed mutation in F2 line | Not yet available |
| sa33933 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa26804 | Splice Site, Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa16143 | Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa1817
Status:
Confirmed mutation in F2 line
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:
Missense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000007353 | Missense | 131 | 313 | 4 | 9 |
| ENSDART00000007798 | Missense | 131 | 600 | 4 | 16 |
Genomic Location (Zv9):
Chromosome 6 (position 41386067)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 6 | 41457667 |
| GRCz11 | 6 | 41455203 |
KASP Assay ID:
554-1809.1 (used for ordering genotyping assays)
KASP Sequence:
TATGTCCCCTGTTGATGACACATTCATTTCTGGCTCCCTTGACAAAACCA[T/A]TCGTCTGTGGGACCTTCGCTCGCCTAACTGTCAAGTAAGCTGTTTTTTAA
Long Flanking Sequence:
TAATCTTGTACACATTAGTTAAATAACAGGTTTTTCCTAAGCTTTACTACTGGTATTTGTGTATGGCTGTTTATCCTTGCCTGTTCTGGGTTGAGGTAGTTGTTTGTACAGTTTTTAGGGTCTGTTATTCTGCCCTGTTAAGGAGCTAACTGTACAGACTACTGCCTTGCCCAGGGTTGAGCCCACTCATCTGACATGGTATACAGTACATGTTTATATTTTTTCTAATAAAATCTTGTTCTAGTTGTTATATTTTGACACATTTGTGCTGTCACAGATACTATACGATACCTGTCTCTACATGACAATAAGTACATTCGCTACTTTCCTGGACACAATAAAAGGTGAGGAACCGTGCCATTAAATTATCATCCTGTTTTTACTATTGAATATTGGTGTTATATGGCTTTTTGTGTGGGTTTTATGCTATTCTAGGGTTGTCGCCCTGTCTATGTCCCCTGTTGATGACACATTCATTTCTGGCTCCCTTGACAAAACCA[T/A]TCGTCTGTGGGACCTTCGCTCGCCTAACTGTCAAGTAAGCTGTTTTTTAATTTGGGTATGTTTTTCTTGTTAGTGTGTACTTGATTCTAATCATGGTTGTGTTCACAGGGCCTCATGCACCTGCAAGGGAAACCTGTGTGCTCATTTGATCCCGAGGGGTTGATTTTTGCTGCAGGAGTGAATTCTGAGATGGTCAAACTTTATGATTTGCGCTCTTTTGATAAGGTAACTTTATACATTTGCATTCAAAGAACTGTACTGTTATATTGGATGTTTTAAAAGTAAAAAAAATTCTTGTCTCAGGGCCCATTTGCCACATTTAAACTGCAATATGAGCGGACGTGTGAGTGGACGGGTCTCAAGTTCAGCAATGATGGAAAGCTCATTCTGGTCTCCACCAATGGAGGAACACTCAGAGTGCTGGATGCTTTTAAAGGAGCTGTTCTCCACTCGTTTGGGGTAAAAAATACTTTTTTTTTTTTTTTTTTTTTTTTTTGTAA
Associated Phenotype:
This allele has been associated with this phenotype by genetic linkage analysis and may not be causal.
See FAQs for more info.
See FAQs for more info.
| Stage | Entity | Quality | Tag |
|---|---|---|---|
| Larval:Protruding-mouth ZFS:0000035 |
brain ZFA:0000008 |
hydrocephalic PATO:0001853 |
abnormal PATO:0000460 |
| Larval:Protruding-mouth ZFS:0000035 |
head ZFA:0001114 |
decreased size PATO:0000587 |
abnormal PATO:0000460 |
| Larval:Protruding-mouth ZFS:0000035 |
inner ear ZFA:0000217 |
decreased size PATO:0000587 |
abnormal PATO:0000460 |
| Larval:Protruding-mouth ZFS:0000035 |
melanocyte ZFA:0009091 |
quality PATO:0000001 |
abnormal PATO:0000460 |
| Larval:Protruding-mouth ZFS:0000035 |
pericardium ZFA:0000054 |
edematous PATO:0001450 |
abnormal PATO:0000460 |
Mutation Details
Allele Name:
sa33933
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000007353 | Essential Splice Site | 257 | 313 | 7 | 9 |
| ENSDART00000007798 | Essential Splice Site | 257 | 600 | 7 | 16 |
Genomic Location (Zv9):
Chromosome 6 (position 41389577)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 6 | 41461177 |
| GRCz11 | 6 | 41458713 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCATTTTGGAGGCTTCTTTCACACCAGACTCTCAGTTCATTATGATCGG[T/G]AAGTCTTCACTTAAGCTTCTCACAGGACTACAAAAGGACTTAAGATGAGT
Long Flanking Sequence:
CATATTGCACCGCTTGCTTGTGTGCGTGCTGCGTTCAATTCAAACTAGCTTAATATATTACTCTCTGTAGATATTTCACTCATTTGCACATATTTCTCTGTGCATGAACCACAAATGCTCAGTGAAAGAGCTAAGTTCACTCATAAAGTGCCGATGGGACATTTCTATGAAGTATGTACTTTTTCATGCTGCTTGCTATAGTGCTACTGTGCTCTCATGGCATTTCTGGTAAATTGACACCTATTATTTAATGGGCTTGTTTTTTTTTTAACCAATGTAATTTAATCTTTTGAGGTAAAAAGTTTTTCAAAAATACTTAATATTACATCATAAATTAATAAATAGCCTAATTATTACAAAGCATTTATGATTATATTAGAAAAAAGCATAATAAGGCACTTTTAAGAGTGTTTCTCTTTCTTACTGCAGGGTTATAACAACAGTAAAGGTGTCATTTTGGAGGCTTCTTTCACACCAGACTCTCAGTTCATTATGATCGG[T/G]AAGTCTTCACTTAAGCTTCTCACAGGACTACAAAAGGACTTAAGATGAGTTTACAGAGATTGATCGTGTCTCCTCAACATTTCCAGGATCAGAAGATGGGAAGATCCATGTGTGGAATGCTGAGAGTGGGATGAAAGTAGCGCTTCTGGATGGGAAACACACTGGTCCTGTTACCTGTCTACAGTTTAACCCCAAATTCATGACCTTTGCCAGTGCCTGTTCTAACATGGTAAGACTTAACCGAAGGTAGACACAAATCTGATGTTTGGCATAACTTACTGTATATTATAGATGGAATATGTGCAATTTGTCACATTTTCGAAACTTGGAGGTAGTTATGAATTAGTTAGTCTTAGATGTCATGCCAAACACTGCTCACGGACATGTGGCTAAATGTCTGATGCATATGGCACACTTAATTGGAAACACTTTAACAGATCATCAGTTGTCCTCTGATTTCTGGGAGTCTAGTGTACAGCAATCTGAACCAGTCCACATGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa26804
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:
Splice Site, Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000007353 | None | None | 313 | None | 9 |
| ENSDART00000007798 | Splice Site, Nonsense | 394 | 600 | 10 | 16 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 6 (position 41416990)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 6 | 41488590 |
| GRCz11 | 6 | 41486126 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAAAGAGTTTGGTGGTGGACACGTCAAAGATGAGATGTTTGGCACAGTT[G/T]AGGTAAGCAGAATGAGTTTCATTTCATTCATTCATTCATTCATTCATTCA
Long Flanking Sequence:
GTTTTTCTTTCAGACTGTAGGGTCATTCTAAAAACTTTGTTGTTGTTGTTGTTTTATTTTACTTCATTCATTCATTAATTTTCCTTCGGGTTTGTCTCTGATTTATCAGGAGTTGCCACAGCGGAATGAACCGTCAACTACTCTGGGATATGCTTTATCTTTAAGCCGCAACCCAGTACTGGGAAATTGATTTTACTTAAATATTTCAATTACTTCAGTCACTTGCTATTTTGTTTGCAAAATTTGCTGTAAATTTTTGACCATTGTCTTGAATCTATCCAGGACATTCTTGCGATTCTTGCTACCATTTTTGTTTGAAAATGTAAAAAATCGAATTGTAATACAGCACATATTACCACACTATAGATGATTCATTCAGTAAACTGATCATCTACCTTTCACTGCAGGTCCGACAGAAGATGCTTTACGCTGCCACTCGCGCCACAGTGAAGAAAGAGTTTGGTGGTGGACACGTCAAAGATGAGATGTTTGGCACAGTT[G/T]AGGTAAGCAGAATGAGTTTCATTTCATTCATTCATTCATTCATTCATTCATTCATTCATTTTCCTTTGCCTTAGTCCCTTATTTATCAGGGGTTACCACAGCAGAATGAACCAAAAATCATTTTAGCATACAGTATGTTTTACGCTGCAAATGCCCTTCCAGCCGGAACTCAGTACTGGAAAACACATACACTCACATTCACACACATATTCACACCTTACAGCCAATTTAGTTTACCCAATTCACCTATTAACCTTATTCTACAATGCGGAAGTGTGTTCTTTTTTGCGATTGTTTTAGAACTTCCGATTCAGTTGCCTATGAGAAAAATGACTAGGAATAATAAATAGCAGAAAACGGTCAAACTACTTGCTCTACAAACAAGTGCTTGCATGAATATACAGACAAAGATGAATAATATAATAAGAAAATGTCATCAAGCAGCAAAATGAGCTGTTTTTAACGTCTAAAAATGAATGGGAGTGGGAATGAGTCTGCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16143
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:
Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000007353 | None | None | 313 | None | 9 |
| ENSDART00000007798 | Splice Site | None | 600 | None | 16 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 6 (position 41424272)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 6 | 41495872 |
| GRCz11 | 6 | 41493408 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCAGTGTGGACCCCAAACATCAGACTCTACAGGGTCTTGCTTTTCCMTTA[C/T]AGGCTGAAGCCAAACGTGCTTTAAAGCASCTCGCAGAGAGACGCATCAAC
Long Flanking Sequence:
TAAATTAAAAACAATGAAAAGTAAATTTAAAGTAAGTCAAACATAACAAAATTATCGCAAAAGAAAACAAAAATTTTTAAGTAGAATTCTTTTTAAAGCTATGAAACTGATAGTCCTTAATAGTAAACAAAAAGAAAACAGGGCTTTCTGGTAAAACAAAACATATTTCGGTGTCAAGTGAGGACAGTTCTAAACAGGTGTGTTGTGATTCAAATATACAGTCATTACATTCATTCAGCATATTACCACTCTGCTTTTCCATTTACTCTTATCCACCATCTCCACCCACATAAACATACTTTTCCAAACAACACAACTGCCATATAATAAGTCTTCCAGCACTGGATCATAGGAATTGTTTTGGAAAAAGGTTTTGATAGATTGGCTGGAACTGTTGCTGCAATACAAACTTTGTATGTGTGTGTATGTGTCTGCAGGTGAAGGCTGAGATCAGTGTGGACCCCAAACATCAGACTCTACAGGGTCTTGCTTTTCCATTA[C/T]AGGCTGAAGCCAAACGTGCTTTAAAGCAGCTCGCAGAGAGACGCATCAACTACATTCAACTGGTACGACACCTTCATATTACACTGCCCTCCACTAATACTGGCCAATGAGGCAAAAAAAAAAGTTTGTTGTTTAACCTTTTGACTTTCGACTTAAAATACTGACAATTAAAGTTGGGGTGGCATGGTGACTTAGTGGTTAGCACTGTCACCTCACAGCAAGAAGGTCACTGGTTTGAGTCTCGGATGGTCAGTTGTCATTTCTGTGTGGAGTTTGCATGTTCTCCCCGTGTTCATTCCTCCAGTGCTCTGGTTTCCGCCACAGACCAAAGACATGCAGGTGAATTGAACAAACTAAACTGACCGTAGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTGTGAATGAGAGAGTGTTTGGGTGTTTCTAAATAC
Associated Phenotype:
Not determined