ZMP
wdr67
Ensembl ID:
ZFIN ID:
Human Orthologue:
WDR67
Human Description:
WD repeat domain 67 [Source:HGNC Symbol;Acc:30888]
Mouse Orthologue:
Wdr67
Mouse Description:
WD repeat domain 67 Gene [Source:MGI Symbol;Acc:MGI:2684931]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa42725 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa36133 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa45575 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa42725
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000114528 | Nonsense | 331 | 1070 | 7 | 22 |
Genomic Location (Zv9):
Chromosome 16 (position 27539228)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 25384915 |
GRCz11 | 16 | 25299947 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAGGTCACCATATTGTCGCAGTGATGGACAGTGGAGCTATTAAAATCTA[T/G]GATGTGCGAAGTCTCACCACAGAAATCAGTAAGGTAAATTACTCTTCATG
Long Flanking Sequence:
GATGCCTTCAAATGTCAAGACAGTAAGATATCTGGATTTCCTGCCAGATAGTTTTGATGACGGATCCAACCAGGTACTAATCCCTTTGCAACTTTAACATTGTGCCCTAGTATTTACTTTATTGTAATACTCGTTTAAAATCTACTGCATGCCTTTACAATGCACAGTCTCTTTGGACTTGGTCTATTGGAATGTATTATGTTCTTGTCAGAAGAATAACTAATATGTAACAATATCTGTTATAACTATAATGAACCTTATTTGAAAAGTTCACATCTAAGATTCATGTTATAAGGTTATTGTTGAAAACACATTGTAATGTTCTCTCTTCAGACTCTAGGTGTTTTAAGCCAAGACGGCATCATGCGCTTTGTCAACATCCAGTCATGCAAGCAGCTCTTTTTAATCGGATCCCACGAGGATGCAATCAGCTCTGCAACTGTTTGTCCTAAAGGTCACCATATTGTCGCAGTGATGGACAGTGGAGCTATTAAAATCTA[T/G]GATGTGCGAAGTCTCACCACAGAAATCAGTAAGGTAAATTACTCTTCATGTTTATTAATTGAAAGTTTTTCATTAATTGTTAGTTATTACACTTAGACACAATAACCCTTTATCAGGCATCATAGCCACCTGGTTGACCTTCTATCCATAGGCTATCAATCTTATTTTAGTCGCTTATTACTATTTATTAGAGATGTGTCAGTATATTATTCAATCCAAGATGTGAGTCAAAAAATTATTTTTGAGGAGTGCATGTTAAAGGGTTAGATACACCTAAAAGATAAAAGTTTTCATCAACTATTAAACAGCACAACTGCTTTCATCATTGATAACAAGAAATATTTCTTAGACCGCTTACCAATGTTTATGTTCAGAATGCCGACAAATGTAAAAAAAAATTTTAATTTAGTTTTTTACTAGCATATTGCTTATATTTTAAATAACTGCTGGTAATAAGGTGCCAAATGTATGTATTTAAACTTAAAGACATCTGTAAATAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36133
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000114528 | Nonsense | 722 | 1070 | 15 | 22 |
Genomic Location (Zv9):
Chromosome 16 (position 27547994)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 25393681 |
GRCz11 | 16 | 25308713 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGCTGCATGCTGAGGCGGTCAGACAGCAGGCTGAGTTTGAGGCCTGGTA[T/G]AAACAGCAGGAGCTGCTTCTGCAAGGAGAAGAGCAACGGAGACTAATCCT
Long Flanking Sequence:
TCAAAGGTAAAATGAATATTATTAAGCTGTTTATTAACAGTAGTTATAGAGGTTTCAAAACAAATGCAGACATTACATGCATTTATTATTATGTTGATCTTCCCCAATGTAGTACTTTTTCCATCATCGCAATAGTTTGGACATTGGTGCTATGCTGAAGGAAACCTATCGGTTGATGGACAGAACCCCTGCCGACATCCATCCTAGCTCTGCGCTGAATGATTTTGAACCTCTGACTCAGGGCCAGTATCCTGTCTTCAACAAATACCCCACATTCATAGTGGAGTACCAGTCTCAAGAACGCGAGAGGATCCGCCAACAAGAAGTGGAATATCTGAGAGAGAGGTGCAAATTCATTTGAAAATCTGATATGGCTGATCATTTCAAATGATATGCAGCTTTTACAATAGGCTTTGTACTTGTATTGCTCTGTATAGACAGGAGGTTCAGAAGCTGCATGCTGAGGCGGTCAGACAGCAGGCTGAGTTTGAGGCCTGGTA[T/G]AAACAGCAGGAGCTGCTTCTGCAAGGAGAAGAGCAACGGAGACTAATCCTACAGGAAGAGGAGAGTAAACTCGCACAACAGAGAGCCAGGTGAGACTCACATCATGTGTCTGATCTCTCACTAATGACTAGATTCATGTGTTGTCATTTCATGGTTCACCTGATGTATTTTACTGTGCTCAGATTGGCCGCCATGAAGCGCGAGCTGAAGGTGAAGGAACTCAGTCTGATTGATTCCTCCAGAAGACGTTTTCTCAAACACCAGCAGGATCAGCGCAGAGTACACCTCAAGAGACTTGATGATGAGATTCAGAGAAAGGTTTAATTTAAGGACCTATATTTCAAAAATTACTTTTATAAGGGGTTTAAACACCATTCTGTGCCAACAGACTGAATGTAACCAACTTCTCATGATAAAAATATATATTTATTTATTTTATGTTTTATAATTTATTTATTTTATTATTTTTTATCATTTATTTATTTTAAAATATTTATTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45575
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000114528 | Essential Splice Site | 942 | 1070 | 20 | 22 |
Genomic Location (Zv9):
Chromosome 16 (position 27553587)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 25399274 |
GRCz11 | 16 | 25314306 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTCATTCTAAAAAGTGACTGTTCTTTAACATTATTTTGGTATGCTTTTA[G/A]TGGGATGATATAGTAGCCAAACAAGCCGAACGTGAGGACAAAAGATGGGC
Long Flanking Sequence:
ATTTGATTACTGATTTCCATGTAAACACAGTCACTGTCTTTTTCCCCTGTGTGTGTGTGTTTGTTTTGCCTCTGTGAACGTCGGCGCGTGCCAAAACCGACACTCCTATTTTTATGCAAATTTTTACAGACCTTCCCTCTTTTGCTCCTCCGACACTCCCCCTAAACAGAGCTGGACACGCCCACTTTCCTGACTTTTTCCAAAGTAGAGGCGTGAAAAAACCCTGCTGAAACAAGGGGGTTTCATGACCCTTTAAAGTTGTTCACCAGCCATTGGCAAGTTGTTTCAAACTTTGATTTATTATTATTATTTTTTATTAAGTGCTGAACTTCCAGTTGCATTAACTGCTTTTTTGAGCACACACAATTTTTTCACAGTTTTAGTAAATGTGGCCTTTATTGTTTTATTTTGATACAGCGAGTACACAGACTGTTAAGTAATGCACTTCACTTTCATTCTAAAAAGTGACTGTTCTTTAACATTATTTTGGTATGCTTTTA[G/A]TGGGATGATATAGTAGCCAAACAAGCCGAACGTGAGGACAAAAGATGGGCGGCTACTTCTGTTACCACTCAGCCGAGGTCATTTATCTCACAGGAAACAGAAGAGATCGAGCAACACAGCAAACCACACAAGACCCTTGATGATTCACTGAGTAAGTTGAGAGAAACATAATAAAGCTTTCCTAATATAGTTAAACGGAGTAATGCAATCAACTACTGTACAATTACTTCTTGACTGAATCATTTATATGAATGTTTGTTCAGCTAGAGTTACTCTAGTTGTTCGTTTTCATTCCTCCAGATTTGCTAGGAATATCTTGTAATGTGTATGTTGCAGATCCTCAGAAGGAAAAGAGACGTAGATCTCCTTGCTCGTCCAGAGGGCTTCTGTACAAACCCACTGACATTTCTTCAAACAATCAGTCAGACTGTGAGTATGATCAGTATAAACTATAAGTGTGTCATGACCAAGCAGAATAAATAAAGCTCTTTCATGTGTGC
Associated Phenotype:
Not determined