ZMP
wnt11r
Ensembl ID:
ZFIN ID:
Description:
protein Wnt-11 [Source:RefSeq peptide;Acc:NP_571151]
Human Orthologue:
WNT11
Human Description:
wingless-type MMTV integration site family, member 11 [Source:HGNC Symbol;Acc:12776]
Mouse Orthologue:
Wnt11
Mouse Description:
wingless-related MMTV integration site 11 Gene [Source:MGI Symbol;Acc:MGI:101948]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa2545 | Nonsense | F2 line generated | Not yet available |
| sa27632 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa2545
Status:
F2 line generated
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000099880 | Nonsense | 273 | 352 | 5 | 6 |
Genomic Location (Zv9):
Chromosome 10 (position 33071773)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 32173122 |
| GRCz11 | 10 | 32116982 |
KASP Assay ID:
554-2463.1 (used for ordering genotyping assays)
KASP Sequence:
GTCCCGAAAGACAWYGACATCCGGCCCGTGAGAGAGAATGAGCTGGTGTA[T/A]CTRCAGAGCTCRCCRGATTACTGCATGAAGAACGACAAGTTGGGCTCTTT
Long Flanking Sequence:
GGCGAGTAAGTAGTGAGTAAATTTTGATTTTAGGGTGAACTGTGCTTTGAGTATGACAGGACAGTCACGAATGAAGTCTGATGTCAATTAAAAACAATCGGAACCACATTTGCGATTAAAATGATTGAATTTCAAAGTCTTTTTTTTATTTGGGACACATGAAGTCATGCAAAAGCCATCCAAAGTCACTAATATGTTACATTCCCTGTGTCATAATGTAATTTTTTTTATTGGATTTATCTTAATCGATCGTGCATTTTTCCATCTCCACAGGCTTTGCGAGATGCTTTGGTCATGAAGTGCAAATGCCACGGTGTTTCTGGTTCCTGCTCCATACGGACCTGCTGGAGGGGCTTACTGGACCTAAAGGACATCGCCATAGATCTAAAGACCAAATACTTGTCCGCAACTAAAGTGGTCCATCGGCCAATGGGAACACGCAAGCAGCTCGTCCCGAAAGACATCGACATCCGGCCCGTGAGAGAGAATGAGCTGGTGTA[T/A]CTGCAGAGCTCACCAGATTACTGCATGAAGAACGACAAGTTGGGCTCTTTCGGGACTCAGGACAGGTAAATCATAAATTATATACCTCTGTTTTTTCTCATTTTAAATTTGTTTTCATTTTTCTTCATTGAGCCCAGTGTGATCAGATTTATTTATTCATTTGCACCATGAGAGTCCAACAATTCTCCCCACATTCTTATATGAAAAAAAAAAATTTATTATACCCATATAAATATATATACCCATCCCAAATAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACCCATCCCAATTTACTTATTTTTCAAACTATATTTTTTATTAATATTAGCTATTTATAATATAATTAGTTATTAATATTAGTTTTTTTGTTAGTTTTATTATTATTTTTATTATTTATTATTATTAAAAAATAGTAATCATATATATTAGCAAAAAATCTGCAAAATAAATAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa27632
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 |
|---|---|---|---|---|---|
| ENSDART00000099880 | Essential Splice Site | 295 | 352 | 5 | 6 |
Genomic Location (Zv9):
Chromosome 10 (position 33071840)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 32173189 |
| GRCz11 | 10 | 32117049 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTACTGCATGAAGAACGACAAGTTGGGCTCTTTCGGGACTCAGGACAGG[T/A]AAATCATAAATTATATACCTCTGTTTTTTCTCATTTTAAATTTGTTTTCA
Long Flanking Sequence:
CGAATGAAGTCTGATGTCAATTAAAAACAATCGGAACCACATTTGCGATTAAAATGATTGAATTTCAAAGTCTTTTTTTTATTTGGGACACATGAAGTCATGCAAAAGCCATCCAAAGTCACTAATATGTTACATTCCCTGTGTCATAATGTAATTTTTTTTATTGGATTTATCTTAATCGATCGTGCATTTTTCCATCTCCACAGGCTTTGCGAGATGCTTTGGTCATGAAGTGCAAATGCCACGGTGTTTCTGGTTCCTGCTCCATACGGACCTGCTGGAGGGGCTTACTGGACCTAAAGGACATCGCCATAGATCTAAAGACCAAATACTTGTCCGCAACTAAAGTGGTCCATCGGCCAATGGGAACACGCAAGCAGCTCGTCCCGAAAGACATCGACATCCGGCCCGTGAGAGAGAATGAGCTGGTGTATCTGCAGAGCTCACCAGATTACTGCATGAAGAACGACAAGTTGGGCTCTTTCGGGACTCAGGACAGG[T/A]AAATCATAAATTATATACCTCTGTTTTTTCTCATTTTAAATTTGTTTTCATTTTTCTTCATTGAGCCCAGTGTGATCAGATTTATTTATTCATTTGCACCATGAGAGTCCAACAATTCTCCCCACATTCTTATATGAAAAAAAAAAATTTATTATACCCATATAAATATATATACCCATCCCAAATAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACCCATCCCAATTTACTTATTTTTCAAACTATATTTTTTATTAATATTAGCTATTTATAATATAATTAGTTATTAATATTAGTTTTTTTGTTAGTTTTATTATTATTTTTATTATTTATTATTATTAAAAAATAGTAATCATATATATTAGCAAAAAATCTGCAAAATAAATAAATAAATCAAAATAATAATACAAACATATTGCACATTGTTATTATTATTACCATTATTATTTTAAGAGTA
Associated Phenotype:
Not determined