ZMP
A4QN61_DANRE
Ensembl ID:
Description:
LOC567031 protein [Source:UniProtKB/TrEMBL;Acc:A4QN61]
Human Orthologue:
WDR47
Human Description:
WD repeat domain 47 [Source:HGNC Symbol;Acc:29141]
Mouse Orthologue:
Wdr47
Mouse Description:
WD repeat domain 47 Gene [Source:MGI Symbol;Acc:MGI:2139593]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa38165 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa19379 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa38165
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000083218 | None | None | 437 | None | 13 |
ENSDART00000121497 | Nonsense | 402 | 894 | 7 | 15 |
Genomic Location (Zv9):
Chromosome Zv9_scaffold3544 (position 69796)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 24549133 |
GRCz11 | 22 | 24576757 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATCTCCAGAGCACAGGCTGAGACAATCAACAGCCCTGGTGGAACAAACT[C/T]GATACGTCCTCCACTCACTCCTGGCAAAGATGGAGGAGTCACAGCTACAG
Long Flanking Sequence:
TACTTTTAATATTAATAACAACAACATGTATTATTATTATTATTATTATTATTATTATTATTATTAATAATAATACTTAAAAAAAATTGTGATTAAAATATTTTTGAGCAACCACTTAGCTTATTACGATGATTTATAATCTAATTCTAATCTTGACGCTGTGTTACTGAGACTGCAGTAATAATACTGTAAATCCAGCTTTGCATCTCAGTAATTAGTTGCCAAAATCCCTTAGATTTTTTTTTTTTTTTTTGGTTTTTAGCTAAAACTGATGATAAAAATGATTGTTTTAAATGCTCAAGTCCATGCAGTTACTTTTAGAAGTACATTTTCTGTTATTATTTAATACATAGTTAATTACCAGCTTATATATAAATACATTGAATATCTGTGCATCCATACTGTATAAAGGTGTTATTATGGCAATTATTTTTGTCTGCCATTTTCGTTTATCTCCAGAGCACAGGCTGAGACAATCAACAGCCCTGGTGGAACAAACT[C/T]GATACGTCCTCCACTCACTCCTGGCAAAGATGGAGGAGTCACAGCTACAGCTGACAAATCTGAGGTAACATAATTAGCTCCCATTTAGACCAGAAACATCAAGACCCTATTTACACCCATCAAAAGGGATAATTCACCAAAAGATTTACATTTCTTTCCTATTGACAAAAATTGAAAGTGATTTAATTGCATGATAATGAAATCAAGTTAACGTTCTGTGACATTAAAAGATATTTGTATAGCTAATGAGCTCGCTATTAAGAAAACCTCAGATTTGAACAAATATGATATGTTTCAATAATTGATGTACTGCACTGTACTGCACTGTACACTGTACTGCACTTATATGTAAAAAACAAATGAAACCAAAAACAAAAAAAACATCAACATTTGAATTAAAATGTGCTTTTAATAGTAAAATGGTAGGTTACTGTTTATAAAAAGTAAAAAGAAAACTCCTGTACTTAAGTTAAAAGTATTAACATATAGTAGCCAACTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19379
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 |
---|---|---|---|---|---|
ENSDART00000083218 | Essential Splice Site | 104 | 437 | 8 | 13 |
ENSDART00000121497 | Essential Splice Site | 561 | 894 | 10 | 15 |
Genomic Location (Zv9):
Chromosome Zv9_scaffold3544 (position 61734)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 24557195 |
GRCz11 | 22 | 24584819 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTAAATGAACGCAGTTTGAGGCCTTAATCTAAATGATATTTTATGACA[G/A]TGTGTTCCAGGATGAGAAGCCCAAATCCCCTTTCATAGCAGTGCAGACTC
Long Flanking Sequence:
TCCAAGTTTTCCAGTTGTCAATCTTAGCCAATCATATTTGTTTATTTTGGGTGAACTTTGAATTTTCGTGACCAGCGCAGAGCCATGGGGGTCAAGAGAGGCAGGTCGTCCTCTCCCAGATGTCATATATCTTCCACTACACTGTTGTCCAGATATCCACAGGCCTCAGTGTTTTCTCTATCATTCGTGTAGGTCCATTCAGAAACTGGAGGAGCTGAATGTGGGAATGGAGGATTTGGGTGAAGACGTTCAGGCTTTGGCTCAGCAGTGTAACGGCACGTCAGCGAGTGAAAGCAGTAAACAGACCCCAGAGACCGGCCCGGGACGAATAAAGACGGCGGTGATCAGCAGCACCCCTCATAAAGGAGGAGTACGAGGGATTCCATCTCTGGATGAGTCCCCAGTGCTGGTCAACCAGAGGTTTCCAAACATTTTGACACTTGTTTTTTTTTTTAAATGAACGCAGTTTGAGGCCTTAATCTAAATGATATTTTATGACA[G/A]TGTGTTCCAGGATGAGAAGCCCAAATCCCCTTTCATAGCAGTGCAGACTCTGGAGGACACGCAGGCGGTGCGTGCTGTCGCCTTCCACCCATCTGGGATGCTCTATGCTATTGGTTCCAACTCCAAAACACTGCGCGTCTGTACTTACCCACAGTCCCTCAAAACCAGGTTGGTTCTCAGTAAGGATGAGCATTTAAATTTGACTTTTAACTAAAGAAGATAACAAGACACAAAAATGTCGTTCTGCCTCTGTATGTTCATCCTATATAGCCCACAAGCTCCAGTAAAACAGCCTGACATCTGCTTCAAGCGTATTAAACACCATAAGGGCTCTATATATTGTGTGGCCTGGAGCCCCTGTGGGCAGCTGCTTGCCACAGGCTCCAATGACAAGTATGTCAAAGTTCTTCCTTTCAACGCTGACACCTGCAATGCCACAGGTAATTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTAATCTAATCT
Associated Phenotype:
Not determined