ZMP
wdr69
Ensembl ID:
ZFIN ID:
Description:
WD repeat-containing protein 69 [Source:UniProtKB/Swiss-Prot;Acc:Q1LV15]
Human Orthologue:
WDR69
Human Description:
WD repeat domain 69 [Source:HGNC Symbol;Acc:26383]
Mouse Orthologue:
Wdr69
Mouse Description:
WD repeat domain 69 Gene [Source:MGI Symbol;Acc:MGI:1923089]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa45651 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa2977 | Nonsense | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa45651
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000024202 | Essential Splice Site | 106 | 415 | 4 | 13 |
| ENSDART00000142790 | Essential Splice Site | 106 | 418 | 4 | 12 |
Genomic Location (Zv9):
Chromosome 18 (position 44795101)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 18 | 46388630 |
| GRCz11 | 18 | 46386648 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCACATCTTGCCCCTGACGAATGTAGCCTTCAATAAATCAGGATCTTGG[T/C]GAGTTTATCAGCTGCGCTCACATGCCTCCCTCTCTCCGATCCTCCCTCTC
Long Flanking Sequence:
TCACAAACAGAGGTTTAATAAATGCAGCAAATCATATTATAATAACTTCTAAAGGATCATTTAACACAGAAGACTGGAATAATGATGCCAAAGAAATTCAGCTGTGATCACAGAAATAAAAAATCCTTTAGAACACAATTTCTAAAATATTTCACTGTACTATTTTTTATAAGCATAAAGACTTCTCCCAAAACTATACTACTTCTAAACTAAATAGCTAAGTGAAATGCATTTGAATGATTTTCTGGCTAAGAACAGGACATCTAATATCACAAATGCCCACTGGGTGGCAGCAAAGGGAAACACCGCTGTGTTTATACATCAAAGGCATGGTAATTAAGTATGGAAATTACACAGTGAAGCTTAAAGATCTGAAATAAATTAATGTGGTTAAGTGCTTCCCCCTCCCGAGTATTTGTCCTCTCTGTCTTCATCTACAGGCACTTCAGGCTCACATCTTGCCCCTGACGAATGTAGCCTTCAATAAATCAGGATCTTGG[T/C]GAGTTTATCAGCTGCGCTCACATGCCTCCCTCTCTCCGATCCTCCCTCTCCCCTTCACTTTCCGTCTGTTTGCAGCTTTATAACCGGAAGCTATGACAGGACCTGTAAAATATGGGACACTGCATCCGGAGAGGAGCTGCACACTTTGGAGGGTCACAGGAACGTTGTGTATGCCATCGCCTTCAACAACCCTTACGGGTAACAGCACCGCTCTCGCTCATTTCATCACGTATGTCCTGAAACACTCAGAACAGCTCTTTTTTGGGGATGAAATAGAAAGCAAACAACCATCTCTGTCTGATTCTGCAGGGTTAGGGCACTGCAGGGTAACTGGTGTTGTTATTACAATGGGACCATTTGTCACTTTGAGTCATAACAGGAGCACTTGTCCCTTTTTTCTTCTTCTCTGCCCTCTTTCTCACTGTCTCTCGCTCTCAGAGACAAGGTTGCCACAGGCTCCTTTGACAAGACCTGCAAATTGTGGAGTGCTGAAACAGGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2977
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:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000024202 | Nonsense | 233 | 415 | 8 | 13 |
| ENSDART00000142790 | Nonsense | 233 | 418 | 8 | 12 |
Genomic Location (Zv9):
Chromosome 18 (position 44796609)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 18 | 46390138 |
| GRCz11 | 18 | 46388156 |
KASP Assay ID:
554-3227.1 (used for ordering genotyping assays)
KASP Sequence:
AGGGTCACTTCGCTGAGATCATCTCTCTGTGCTTTAACACAACGGGTGAT[C/T]GATTGGTCACGGGGTCATTTGACCACACTGCCATTTTATGGGATGTTCCT
Long Flanking Sequence:
ATCAGTGAAAACTTAGCCATGCATTTCTTAATTAATGAACTTGGCATAAATCTTTCATTATGATCATTTATGCGGTAATTCAAGCATTCCATTTTGTTTAGCCGCTTGACACAGAATGTAAAGAAATGCATCAGGATGTAAACTGAATATGAGAAACCTGATGTTGGAGCTTTGAGGAGGGTGAGACAGAGCGTGTGGAGGTCTTTTCCTCTCCACAGCACATGGCAGAGCAGTGTGACCGAACGCTCGGTGCGTGTGTGCTGTGTAATTACCCCTCTTAACTCTCCAATTATTCCTCTATGAATCTAAATTATGAATAGCTCTACGAGTTCTTACCGATGAATTGGGGGAATTAATACGATATTTCATTGCTGAGGTAAAAAAAGACTGTCTTTTTATTAGCTCTGGCTTTCTTCATTCAGAGCCTTTGTCTGTTGAATACTTTTTTTCAGGGTCACTTCGCTGAGATCATCTCTCTGTGCTTTAACACAACGGGTGAT[C/T]GATTGGTCACGGGGTCATTTGACCACACTGCCATTTTATGGGATGTTCCTTCTGGCAGGTCAGTGTGTACTGAACGTCACTGTTTGAGACTGATTTACTAACTTATCTTCCTTTCAAAACCAACCATATAGTGCATCCGGAAAGTATTGATAGCGCTTCACTTTTTCCGCATTTTTTATGTTGCAGCCCTATTCCAAAATAGATTAAATTTATTTATTTCCTCAAAATTCTACACACAATACCCCATAATGACAATGTGAAAAAGGAGTAAAAATTAAAAATAAAAATCCTAAAAAATCACATGTACATCAGTATTCACAGCCTTTGCAGTGAAACTCTAAATTGAGCTCAGGTACTTTCTGTTTCCACTGATCACTCTTGAAATGTTTTAGCTGCTTCATTGTAGTTCACCTGTGGTCAATTCAGTGGATTGTACATGATTTGAAAAGGCATACACCTGTCTATACAAGGGCCCAGGGTTGACAGTGCATGTCAAAGCA
Associated Phenotype:
Not determined