Busch Lab

ZMP

A4QN61_DANRE

Ensembl ID:
ENSDARG00000059685
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.
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.
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