ZMP
wls
Ensembl ID:
ZFIN IDs:
Description:
G protein-coupled receptor 177 [Source:RefSeq peptide;Acc:NP_998311]
Human Orthologue:
WLS
Human Description:
wntless homolog (Drosophila) [Source:HGNC Symbol;Acc:30238]
Mouse Orthologue:
Wls
Mouse Description:
wntless homolog (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:1915401]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa25762 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa39773 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa25762
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000016369 | Nonsense | 196 | 542 | 4 | 12 |
ENSDART00000130302 | Nonsense | 196 | 542 | 4 | 13 |
Genomic Location (Zv9):
Chromosome 2 (position 10152622)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 10577718 |
GRCz11 | 2 | 10361317 |
KASP Assay ID:
2259-1624.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGACCTGTTGCCCTTTATGGAGCTTGGCAGTGTGGCCCATAAGTACTA[T/A]CTTCTCAATGTCCGACTGCCTGTTAATGAACGAAAAAAGGTCAACATCGG
Long Flanking Sequence:
TGAGGAATGTGTTTAGGGGTTGAGAGCAATGGTATTAGCATTGAAGCTTGTAGTATCCTTGTTTTTGTGTACTTGCATAATGGAGCACAGTAAACTACTCTACAGTGCAGCAACGTTTACTGTTTAAAGTGCATTAACTTTAAGACCTGTGTTTTGTGTTGTCCTGTAGCGGATGGAGCTTCGATCACCATTGATGTCAGGCTGGCCTACAGAGACGACAAACTGAGCGAGTGGACACAGATGGCCCATTCCGTAGAGCAACGCAAACTCAGCTGCAATTTCACTGCAGCAAAGGTAAATGATCAACTCCATTCTATGTAATTAGGCACTAAATAGGGTACTAGTGGAATCGATTAAAATCTGGTTGTGGTTTTTTTTTTAAACTTTGAAAACTTCAGTTGCTTTATTTTGAATTTGCAGACTATAGAAAATGAGGGTCGCCTCTATGATTGTGACCTGTTGCCCTTTATGGAGCTTGGCAGTGTGGCCCATAAGTACTA[T/A]CTTCTCAATGTCCGACTGCCTGTTAATGAACGAAAAAAGGTCAACATCGGGATTGGAGAAATCAACGACATGCGTCTTGTGGTGAGTCTTCAGAGTGTGACTTTGATGAATAACCTTTTAGGATGCATGTCTAAAACGCACAGCTATGTAGTCGGTTTTGTTTGAGCTTTGTTTGCCTGGGAGGATTTTGGCTAGTCTCGTCTTGTTATAATTGGCACACGCTTCAGGACAGGGCAATGGTTATACAAATGTCAGTGGACCAAGGACATCTGGATTGCATCATGACTTAATCTTCGCCTTTGTTTGGATTACTCCTCTTATTTGACTCTTAGCAAACAACGATACCCATCAATTAAGTGTGCTTAATGTGTTTCTCATTGTCACTGTAACTCTTCAGGGCATTCATCAAAATGGTGGCTTCACCAAGGTTTGGTTTGCCATGAAGACGTTCCTCACTCCCAGCGTCCTTATTATTATGATCTGGTACTGGAAGAGAATCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39773
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000016369 | Essential Splice Site | 325 | 542 | 6 | 12 |
ENSDART00000130302 | Essential Splice Site | 325 | 542 | 6 | 13 |
Genomic Location (Zv9):
Chromosome 2 (position 10145887)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 10570983 |
GRCz11 | 2 | 10354582 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGCCATGCTGCTCTCCTTCTGGATCATCTTCTGTGGAGAGCACCTCATGG[T/C]AAGTGCCAGCTTTCTTGTTTGTTCAAATGTGGATCAATTGGTGCAGAATT
Long Flanking Sequence:
TGCACTTCCTTACCCTCACCAGAGTTGACCTCATGGACATTCCTTGCATTCCAACCCAATATGGTCTTTTTCTGCCACATTGAGCCAGGCGGGAATGTGATTCATGTGTTTGAAGTTACATTCCACACCCCATCTCAGTCTCACCGAATGGGCCGTATAATAGCTTGTCCCAGCATGCCTGCCTTTGAACACTAGAGAACAGAGAGATTTGGTTTGACCTTTTTCAAGGCTTTGGTTCTGTCCTCTTAGTTATATCTTGCTATTAGTGTAATGTTTCTTGGTGAGGTGTGCTAGCAATTATTATACTCTGTACACTGCGTCCTCTTTTAGGGTCATCTTCGCTCTGGGAATCTCCATGACCTTCATAAATATCCCAGTGGAGTGGTTCTCTGTGGGCTTTGACTGGACCTGGATGCTGCTGTTTGGTGACATCCGTCAGGGCATCTTCTACGCCATGCTGCTCTCCTTCTGGATCATCTTCTGTGGAGAGCACCTCATGG[T/C]AAGTGCCAGCTTTCTTGTTTGTTCAAATGTGGATCAATTGGTGCAGAATTACTTTAAACTTTTGTCTTAAAATAAACAATTCTGTCGGAGCCTTTGAGATCTGTACTTTGTTAATACAATTCCCTTGATCTCTTTTCAACTGTCCTATCTTAATGAAGGGAAAAATACACTCTGTCACTTTACTTGGTTAGAAATGGTTTGGACTAATTTTTACCATTATGGCTGCCTTTTTAATTCAAGTCAATAAAAAAATAAAAAAAAATAATTAATCAGAGTTTTAAGATCCATATTGAAATGAAAGCATCATGCTATTGCTGCAGATCCACAATGTAAATCTCGCCTTCCTGCACATCCCAAATCAGATTGAGATATTGGATTGAGATCTGGTGACTGCTACCATTTAAGTATAGTCAACTCATTGTCATGTCCGTGATGATTTGTTTTCCTGCTGGACATAACAGTTAAGATGGTCACACTGTAATCATCAACAACATACGGCT
Associated Phenotype:
Not determined