ZMP
zgc:154085
Ensembl ID:
ZFIN ID:
Description:
WD repeat, SAM and U-box domain-containing protein 1 [Source:UniProtKB/Swiss-Prot;Acc:A0AUS0]
Human Orthologue:
WDSUB1
Human Description:
WD repeat, sterile alpha motif and U-box domain containing 1 [Source:HGNC Symbol;Acc:26697]
Mouse Orthologue:
Wdsub1
Mouse Description:
WD repeat, SAM and U-box domain containing 1 Gene [Source:MGI Symbol;Acc:MGI:1919387]
Alleles
There is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa40647 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa40647
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 |
---|---|---|---|---|---|
ENSDART00000121431 | Essential Splice Site | 225 | 487 | 3 | 12 |
ENSDART00000128024 | Essential Splice Site | 225 | 487 | 3 | 11 |
Genomic Location (Zv9):
Chromosome 6 (position 11923699)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 11777235 |
GRCz11 | 6 | 12012527 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAGGACAGTCTGCTGAAGATATGGATTGTTTCTCTTTTGCCTTCTGCAG[G/A]TAGCATCACCTTATACCCTACCCACCTGTGTCTCCTTTTCTTTCTTTATC
Long Flanking Sequence:
CTGCATCCCAATCATCACAAATACTGCAGCAGACCTATTGGAGCCTGCATGGATCCAAGATTCTCACAGAAATTAGTCAACTTTGGTGACCAAACTAGATCAATTCGAAGTCAAGTTATTATTTATTGTTCCTAAAACTTGGATAGATGACAAGACTTTTGTCAGGTACTGTATCTCTTCAATTACTCAGAAATATTAAGCAGCAATTTAATCTTTCTTGAGCATCAAATCAGCATATTATAATGAGTAAATTTAAACTTTCAGCATAAAAAGTCTCTTTCAGAATAAACTTATGACTTTGACCTGTAGCTTTGGCAGTCTGCAAAATCATTTCCACATGGCTTTCCCTTCTAAGGATGAATCATTTGTTAATAAAAGTTAAAGATGAACTCTCTGTCTGTCTTTACCAGGCACAGATGGCTGTGTTCAGTTTCGACTGGCCTCATGTGGACAGGACAGTCTGCTGAAGATATGGATTGTTTCTCTTTTGCCTTCTGCAG[G/A]TAGCATCACCTTATACCCTACCCACCTGTGTCTCCTTTTCTTTCTTTATCTTTGTTTGTAGCATGTTTGTGTGTGTTTGTGTGTTTGTGTGTTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGATTTAATGATGCATGCTGATCCACAGGCATTAAGATGCAGCTCGCTCACACTCTGACAGGACAGTCTGCTCCGGTTCTGTCCTGTGCTTACTCTCCTGATGGACAGATGCTGGTGTCTGGGTCAGTATTAAACACATGTACACTGCAGGAACTCTAAAGTAACATCATCTTTAAGTTAAAGTACCCAATTAATGCTATTTTTTTATTGGTTCCTAATTTAGTTTCAGATATCTCTTGCAATCCATTTAAAGAAATAAAAAAGAAAGT
Associated Phenotype:
Not determined