ZMP
wdr11
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate bromodomain and WD repeat domain containing 2 (BRWD2) [Source:Un
Human Orthologue:
WDR11
Human Description:
WD repeat domain 11 [Source:HGNC Symbol;Acc:13831]
Mouse Orthologue:
Wdr11
Mouse Description:
WD repeat domain 11 Gene [Source:MGI Symbol;Acc:MGI:1920230]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa15911 | Nonsense | Available for shipment | Available now |
sa35403 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa15911
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000114328 | Nonsense | 258 | 1239 | 6 | 29 |
ENSDART00000136977 | None | None | 897 | None | 22 |
ENSDART00000147490 | Nonsense | 15 | 81 | 1 | 2 |
Genomic Location (Zv9):
Chromosome 13 (position 2541901)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 2625337 |
GRCz11 | 13 | 2758515 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGTKCAGGGCTGAAGCAGTGACTCTTAATGACTGCCTCCAGCTCTCATA[T/A]CTRCCATCTAAGAGAAACCACATGCTGCTGTTGTACCCAAGAGAGATCCT
Long Flanking Sequence:
TCTGTTCTTTGCATATACACTACCTGACTAAAGTCTTGTCGCCTATTTAAGTGTTAGGAACAACAAATAATAACTTGACTTCTAGTTGATCATTTGGTATCAGAAGTGGCTTAAATGAAAAGCAAAGGCCTCTAGATTACACTTATTTTACCACAGTAAAATGTGATCATGCCTTGATTTTTAATGATTTTATTAGGGCAGTAAGGTCTGACTTTGCTTAGACAAAAGTCTCATCACCGAACAGAAGTAATGTCCAGAATATAAAGTCCTGCTGCAGTGGAGACAGAATGAATATTGTGTCTGACTCTCATCATGGCCGGATTAACCAGTTGGGGCCCCTGCGAGGGGCTTTATTTATTATTACTATTGTTTATTTATTACTCATAAATGTAAAGAGCTGAAGATTGAATGTTGAAGATAACGCTGGTGTTGTAAATATGATCTGTGTTTCTGTTCAGGGCTGAAGCAGTGACTCTTAATGACTGCCTCCAGCTCTCATA[T/A]CTGCCATCTAAGAGAAACCACATGCTGCTGTTGTACCCAAGAGAGATCCTCATCCTGGACCTGGAGCTCAGTCAGACTGTTGGTGTGGTGGCTATTGAGCGCTCCGGCGTGCCCTTCATACAGGTGCGTTTGAAGGGAATGCGGGCACATACAGCTGAAGTGTTGCCTCAAACTACAAACGCGTCATGCAGATTCCCCAATAAACCCAATAAATTAACTAAATATGCAAATAAACACACCTCATGCTTCTTTGGGGTGGTGCTGATTAAATTTATAATCTGTATATCCTGCATTTTGCCTTCTGACAAGCCTTAAAGGTGCGTTGCTTAGTAACGCATAAACCATAGATATATACACTAGATGTCGCCTGGCCTATTGTTGTCTATTGGACGGAATGCGTCAATAGCGCCGCCATCTTGCTACAGGGTAGCGCTCCTTTGAAATGAATGCGGGACCAATGTACAGTGGAGGACTGTGGCCATCCAAACCCAGAGATATAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35403
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000114328 | Essential Splice Site | 299 | 1239 | 6 | 29 |
ENSDART00000136977 | None | None | 897 | None | 22 |
ENSDART00000147490 | Essential Splice Site | 56 | 81 | 1 | 2 |
Genomic Location (Zv9):
Chromosome 13 (position 2541776)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 2625462 |
GRCz11 | 13 | 2758640 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACTGTTGGTGTGGTGGCTATTGAGCGCTCCGGCGTGCCCTTCATACAGG[T/A]GCGTTTGAAGGGAATGCGGGCACATACAGCTGAAGTGTTGCCTCAAACTA
Long Flanking Sequence:
AGGCCTCTAGATTACACTTATTTTACCACAGTAAAATGTGATCATGCCTTGATTTTTAATGATTTTATTAGGGCAGTAAGGTCTGACTTTGCTTAGACAAAAGTCTCATCACCGAACAGAAGTAATGTCCAGAATATAAAGTCCTGCTGCAGTGGAGACAGAATGAATATTGTGTCTGACTCTCATCATGGCCGGATTAACCAGTTGGGGCCCCTGCGAGGGGCTTTATTTATTATTACTATTGTTTATTTATTACTCATAAATGTAAAGAGCTGAAGATTGAATGTTGAAGATAACGCTGGTGTTGTAAATATGATCTGTGTTTCTGTTCAGGGCTGAAGCAGTGACTCTTAATGACTGCCTCCAGCTCTCATATCTGCCATCTAAGAGAAACCACATGCTGCTGTTGTACCCAAGAGAGATCCTCATCCTGGACCTGGAGCTCAGTCAGACTGTTGGTGTGGTGGCTATTGAGCGCTCCGGCGTGCCCTTCATACAGG[T/A]GCGTTTGAAGGGAATGCGGGCACATACAGCTGAAGTGTTGCCTCAAACTACAAACGCGTCATGCAGATTCCCCAATAAACCCAATAAATTAACTAAATATGCAAATAAACACACCTCATGCTTCTTTGGGGTGGTGCTGATTAAATTTATAATCTGTATATCCTGCATTTTGCCTTCTGACAAGCCTTAAAGGTGCGTTGCTTAGTAACGCATAAACCATAGATATATACACTAGATGTCGCCTGGCCTATTGTTGTCTATTGGACGGAATGCGTCAATAGCGCCGCCATCTTGCTACAGGGTAGCGCTCCTTTGAAATGAATGCGGGACCAATGTACAGTGGAGGACTGTGGCCATCCAAACCCAGAGATATACACATATACACATATATCTATGATCGGGAGTTTTCCTGGATGTTCGTGTGTAATTTTTTTTTCTAATTTGAAACTTATAATTTTACATCACTTTTCTACATTGATGGATCAGTGTCCGCACGGGCA
Associated Phenotype:
Not determined