ZMP
si:dkey-65b12.4
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to human WD repeat domain 66 (WDR66) [Source:UniProtKB/TrEMBL;Acc:A3QK38]
Human Orthologue:
WDR66
Human Description:
WD repeat domain 66 [Source:HGNC Symbol;Acc:28506]
Mouse Orthologue:
Wdr66
Mouse Description:
WD repeat domain 66 Gene [Source:MGI Symbol;Acc:MGI:1918495]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11751 | Essential Splice Site | Available for shipment | Available now |
sa20505 | Essential Splice Site | Available for shipment | Available now |
sa12207 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa11751
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000083665 | Essential Splice Site | 92 | 906 | 2 | 20 |
ENSDART00000147299 | Essential Splice Site | 160 | 906 | 3 | 18 |
The following transcripts of ENSDARG00000059855 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 43394499)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 41175764 |
GRCz11 | 5 | 41775917 |
KASP Assay ID:
2259-6335.1 (used for ordering genotyping assays)
KASP Sequence:
GCGGACATGGGTCAAGAGAGTCTTGWTATCATATGGGATGCTTATACAGG[G/T]TAAATCTGACCCTTTATTCTATTCCTATTGCTTTTGTAAATCCSCCCTTA
Long Flanking Sequence:
GGTCAAAAATCAATGTAAGTAAATAAAAAAAAATGTAGTTCCAAAAAAAAAAATAGTTCCAATGGCTGAACCCGCACTTATATAGTCAATACTCTAGTTTCTTTTTTCGACCTGTATCTAAAACTTAGTCCATCACACTTCCAGGTCCTTGAATGGGCTTATGGCATCAACTCAACCCTACCTGTTTTCAGCCTGCAGGATGAGGACAGGCTTGTCATCATCTATGCTTGTGCTCATGTTGCTGTCATTTATGATCACACTTCTAAATCACAGTACCTGTTACAAGTAAGAGACTTGTATTGTTTCAAACTTAAATGACTTACAAAATTAAATGTAAAGCCTAAAATGGTATTGTAAACATGCTGATTTTGTGCTGCTTGGTGTCTGCAGGGCCACTGCAGTCCAATCACCTGTCTGTGTACAAGTGAAGACAGACGTTGGATTGTTACTGCGGACATGGGTCAAGAGAGTCTTGTTATCATATGGGATGCTTATACAGG[G/T]TAAATCTGACCCTTTATTCTATTCCTATTGCTTTTGTAAATCCGCCCTTACAACTGACTTTAAAGACTTGATTATCATGCTTATGCATTGGGCAAAACAGATCTTTTTCACATTTAAGTGAAATGGATTTATCAAAAAAAAAAAAAAGAAGAAGAAGTACTGAACTTTTCGGTTGTTGTTTGGAAGAAAGCCAGTCAACTTTATATGTGCTTGTTGTAAACTTAGAGAAATGGGTAGAGTTTAGGCAGACTAAATGAATCGAAATGTCAGAAATAGCATATATACATAGATGAACTGTTCACAGTAAGTTACATTTACCAGCATTTGATACATTGGTTCACCTGTTCATTAACATAATTAATGAATTAGCCAGCCACATGGACATGTTACACATGACTTAAGTGAATTTGAAAGTGGCCTGGATGTTGGTACTAGATGGACAGGCCAAAGTATTTCAGAAAGTGCTGGTATCTACAGGGGTTTGCACACACAACCTAGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20505
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000083665 | Essential Splice Site | 413 | 906 | 9 | 20 |
ENSDART00000147299 | Essential Splice Site | 479 | 906 | 10 | 18 |
The following transcripts of ENSDARG00000059855 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 43398692)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 41179957 |
GRCz11 | 5 | 41780110 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTTTCCTGTCCCACAAACAGATCCAGTGCATTGCCTATGATCCACAAGG[T/G]GAACGTTTCATTGTTGTATTACCATATTTTACGGGTCATTTGTTTGCTGT
Long Flanking Sequence:
TTGTTAAGAAAGAAAAAATACATGGATTACTCTAAAAAACAGAAACAGTAAGAACTTATTTTGTGTTCTATAGAATAAAGTATACTAATTTGGAATGAGGGTGATAAAATAATTTCGTTTTAAAGTATTTCTCTTATGCATTTCCATCTTTTATGTCACCATTTTCATACTTTCTTCAGGCAGGGATATAGAGGCATCATTTTTCAACTCTACAGTGTAATAAACTCTTTCTCTCCTTCTATTTACAGAAATTTTGTCCTCTCTACAACTCATGCAACTGTAGTACATGTAAACACACAGACAAATGTTCCAAAGAGCCTTCTGCGGGAACATGCAGAACCTCTGGAAGCAGTTGCCTGCCATCCTAAACAACCATTGGTAGCTATGGGCAGCCACAGCGGCACCATTAAGGTATGGGATTATCAGCATAAAGAGGCCGTCTGCAGCAGAGTTTTCCTGTCCCACAAACAGATCCAGTGCATTGCCTATGATCCACAAGG[T/G]GAACGTTTCATTGTTGTATTACCATATTTTACGGGTCATTTGTTTGCTGTCAATTTACCCACCCTCAGCCCATCCAAGATGTAGTTGACTTTTTTTAATCAGTGCAACAATAAATTACACTTTTAGCTAAAACTGTTGGTGATTTATAACTTGCAAGTCCATTAACTTAAAAAAAAACATCAGCAGGCAAAATGAAATTATAGAGTTCTTATTAAATGAGATGATTGGTCTGTGTGAGTATTATGTGAAGGGATGCTGACAACAGAGGTGCGGATCCAAATCCAGGGTTTATTAGGAGAATGGTCAGGCAAGCAGCAGTCAACACAGAAACAAACAGACGTATATGGGCAATCCAGAGTCATGGTCAATACACAGGTGAATGGTCAGTAGAAGCAGTCAGCAGACAATGTAAACAAACAAACAAGGCGAGGTCAAAACACGGCAAATTAAGGCAAGAGAAATGCGCTGTAATGTTCACAGTAACAGATGAACAAGACTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12207
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000083665 | None | None | 906 | None | 20 |
ENSDART00000147299 | Nonsense | 903 | 906 | 18 | 18 |
The following transcripts of ENSDARG00000059855 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 43405822)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 41187087 |
GRCz11 | 5 | 41787240 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGGATGAACTGCTTGAGCTACTGCAGGCTAGAGGTAAGTTTTTTATTTTT[A/T]AAGATTGTAATTAACAGAGAAAGATTTTGGTTACTGCATTTAAGAGGCTG
Long Flanking Sequence:
TTAGGAGATGGAGGAATATTTTTACTACTTTCAGCTACTGGACCAAAACCTTGACTCTATGGAAACCCGGCTTGTGTCCACACGCATCCCTCTTGCTGATGTGCCCTTCTTAATGCGAGCCCTTGGCTTCTATCCCACAGAGCAAGAGGTACAAGCACTGTTGCAGTCACCAGTTGACTCTACAATACAGATCTGTCATCAACAGGTGGACTAGCACTCAATATTTTGTCAACCCACTTTTTGTTTTGTTGAAGCTGGAAGACATGCAAAATGAGGTGAAGTTCAGCCGCTATGCTGAAACCAGAAATTATGTGACAGACATCGATCTGGAGGAGTTCATTAGGCTGTATGTCAACCACAGACCTGCCTCTGGCATTTCCAGGCAGGAGCTGTACAATGCCTTCCAGGTGCTTGGAAAGCCAGACGAGGAGGGCAGGTATAATATTGACAGGGATGAACTGCTTGAGCTACTGCAGGCTAGAGGTAAGTTTTTTATTTTT[A/T]AAGATTGTAATTAACAGAGAAAGATTTTGGTTACTGCATTTAAGAGGCTGTGAATTTGGTTATAATATACACTTATATACACTACCTGACAAAAGTCTTGTCGTTGATCCCAGTTGTAAATGCAACAAATAATAACTTGAATTCTAGTTGATCATTTGGAAAAATTGTTTATTTTGGTAGTGGTAGATTTTTTTGTTGAATAATCTGTTGAACTGCATCCCAATCATCAAAATACAACAGAAGACGTATTGGAATGGTTTGGAATCATGGACCCAGAGTTCTAACAAATATCAGTCAAGTTTGGTGAAGGAAAAATTATGGTTTGGGATTACATTCAGTATGAGGGTGTAGGGTCCACCCAGTTGGTCCAATGACGGTATCCAATGGTGGATGAAGGTTCACTGCATGTTCGGTCTTTCCAGTGCACAATGTTGATTTATTTTAAACTTAACTCATATCTGACTCCAATTTTAGTATGAGGTGGTTTAGAATATTAATAT
Associated Phenotype:
Not determined