ZMP
wnt2bb
Ensembl ID:
ZFIN ID:
Description:
protein Wnt-2b [Source:RefSeq peptide;Acc:NP_001037809]
Human Orthologue:
WNT2B
Human Description:
wingless-type MMTV integration site family, member 2B [Source:HGNC Symbol;Acc:12781]
Mouse Orthologue:
Wnt2b
Mouse Description:
wingless related MMTV integration site 2b Gene [Source:MGI Symbol;Acc:MGI:1261834]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa34423 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa34424 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa34423
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000046004 | Nonsense | 257 | 396 | 4 | 5 |
Genomic Location (Zv9):
Chromosome 8 (position 28614441)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 27742359 |
| GRCz11 | 8 | 27761498 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGTGTAAATGTCATGGAGTCAGTGGCTCGTGCACCCTCAGAACCTGCTG[G/A]TTGGCAATGTCAGATTTACGTAAAACAGGAGATTACCTTCGCAAGAAGTA
Long Flanking Sequence:
AAATTAACTGTGGCTAGTGAGCCCTGCTGCTCAATGGCCTTCTCAATCATTTATCAGATTGATAGGCAGATCAGCCTGTCGTTTTGTCATCCTAAAATCAGAGCTGCATATTGGAGTGTGGCACAGCAGTGCACTCAATTTACTTTTTAGAGGGAATAATAAAACATATAAAAAATTATTTTAAAAGTAGAAGTTGAACTTAAACCTCACTTAAGTCTCCCAAAGAATGTAGACGCTTACAACTAAACAACATTATTTTGGCATATAACTGCTGACATACCACCCATAAATCTAACACTAACATTGTTCTATGATATTCCATTCCTGTAAAAATCCTGTTTACATTCTGCGGCCATTTTTGGCCACATGGAATCTGTTCATATAATTACCACTAGGCCTGTTTTGTTCTGTTTCCCTGTTTTACAGGCTGTAAAGCGCTTTATGAAACTGGAGTGTAAATGTCATGGAGTCAGTGGCTCGTGCACCCTCAGAACCTGCTG[G/A]TTGGCAATGTCAGATTTACGTAAAACAGGAGATTACCTTCGCAAGAAGTACAACGGAGCCATCGAGGTCACCATGAACCAAGACGGGACAGGATTTACAGTAGCCAATAAAGACTTTAGAAAAGCCACAAAAAATGACCTGGTGTATTTCGAAAACTCACCTGATTACTGCCTCATGGATAAAACTGCAGGTAAGGAGGAGTAAATACTCATAAACTTTCACATACTCCTTTCAAATACTCTGTGTTAAAAGCTCTCCAAAAGCTAAGGAGCTGCCTCATTGCCTTATTAAACAGGTAGCATGAATTAGGGGTAATAGTTGAGTAAATAGCACATTTATTTATTAAATATTGAATTTATTTATTGTGTTCATTGGGTTAATGTAATGCTACACACAGTATAAATTTAAAGAACAATTCTTTTTTTTATTCATTTCTTATTAAGCTACAAAACAACAAAATAAATCACACTTAGGTTTTTAATAATGCAATTAACACCAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34424
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000046004 | Nonsense | 366 | 396 | 5 | 5 |
Genomic Location (Zv9):
Chromosome 8 (position 28621635)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 27749553 |
| GRCz11 | 8 | 27768692 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACACCACACGCTCAAAACGCATCACCAAGTGCGAATGCAAGTTTAAGTG[G/A]TGTTGCACTGTAGAGTGCAAAGACTGCGAGGAGGCTGTCGACATTCACAC
Long Flanking Sequence:
GGCGTTGCACGTTTACTGCAAGACAAAAAGAGTCATCCATCACGGATTATAAACAATTTTAAAGTAGTCAGAGTGCAGAGTATATGTGTGAGCTCAATGCTGGAGTGCATTAAAGCAATGTAGTTAAACACCAGCGTATTGCTCTATTCTTAACCATGACATTGCAATGCATTGAAAGGGCATTTTCAAAGACCCATATTAGCGCCTCTTAAACAGCCACCAGTGTCATTAATAGCAAATGGTTCTAAATTTTACATATAGTATTTTGTTTAAAGAAATGATGGCAATAAAGAATCTTTACTTTTATTTCTGTATTTATTCATGAGTATTTAACCTGTAATCACTTCTGTTCTGTGCTGTCTAGGTTCATTGGGCACTGCTGGTCGGGTCTGTAACAAGACATCCCGAGGGACAGACGGCTGTGAAGTTATGTGTTGTGGGCGGGGCTACGACACCACACGCTCAAAACGCATCACCAAGTGCGAATGCAAGTTTAAGTG[G/A]TGTTGCACTGTAGAGTGCAAAGACTGCGAGGAGGCTGTCGACATTCACACCTGCAAAGCTCCGAAACGTGCGGAATGGCTGGACCAGACCTGAGATACGCCCACTTCCTGTCGATCCTCAGGATTTTGTCCATGGCATTCTGGGATATGAAGTCCATCCCTTGCGAGTTTTCCACCCCGCTCCCCCCCAAAAAAATCCTTCTTTTTTGTTGCATGGCTTTATTTGAACTTATTTTGTGAAAGCACTACAACTGAAATCTATGAGCGCCTTGCACACTTGGCCTGATATGCCAGATTTATTTTTCTCTCTTTCTTTTTGTTTTAAATTAGTCAAAGGACGGTAAAAGTTGGGGATTCACAAAAAAAACAACAACTGTGCTGTAAAATGTTGGTTTATTTTTTGTTGTTTCGTTTTGACGTAAGAATTTTGTTTTGTGAGTGTTGTTTTGTGACAAAGGGTGTGCTGCTTTTAAATAATATTTTAAACTGACTCTGAGCCTA
Associated Phenotype:
Not determined