ZMP
wacb
Ensembl ID:
ZFIN ID:
Description:
WW domain containing adaptor with coiled-coil b [Source:RefSeq peptide;Acc:NP_001005971]
Human Orthologue:
WAC
Human Description:
WW domain containing adaptor with coiled-coil [Source:HGNC Symbol;Acc:17327]
Mouse Orthologue:
Wac
Mouse Description:
WW domain containing adaptor with coiled-coil Gene [Source:MGI Symbol;Acc:MGI:2387357]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa10649 | Essential Splice Site | Available for shipment | Available now |
sa17642 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa10649
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000012531 | Essential Splice Site | 338 | 494 | 10 | 14 |
ENSDART00000098384 | None | None | 155 | None | 3 |
ENSDART00000012531 | Essential Splice Site | 338 | 494 | 10 | 14 |
ENSDART00000098384 | None | None | 155 | None | 3 |
Genomic Location (Zv9):
Chromosome 2 (position 3082268)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 4554421 |
GRCz11 | 2 | 4395046 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGTCTCTAAACCCCTGCTCAGCTCYGCATCKCTCTCTTCACAACCAAAGG[T/G]CAGTAGCAGAGGTCAATGGGTCATTTTCAAAGATATTAAAGTGGTCTCAG
Long Flanking Sequence:
GATCGGTGCATCTTTACAATTTGTATTACAAAAAAATACAGTGTTTATTTTTTTATACACCTCCAAACCTAGGTCACGGACATGCTAAACTCTTCTAGATGAAGTCTCTTAACTTTATTTTACACTTGACAATTTAGACTTCAGATTGTTCTTCATTTAGTTAAAAGTGTGCTGTGTTTAGAGTTAATTTTGTACATTTGTGGTAAATTACAGCCATCCAAACCTGGCGTGTTCACACAAGACTTTTTTGTACTTGATCTTCTCACACCAGAGTTCTGTATGTTGTATTGTTGTTATTTAAACGTGTGATTATGTGTACGATTATTTTCTAACCGTGTGTTTGTGCTGACCAGCTCAACAGTCCGGTCAGTCACCCATGTCATTAGCATCAGACGCCTCTTCACCGAGGTCATACGTGTCTCCTAGAGTCAGCACACCTCAGACCAATGCCGTCTCTAAACCCCTGCTCAGCTCCGCATCGCTCTCTTCACAACCAAAGG[T/G]CAGTAGCAGAGGTCAATGGGTCATTTTCAAAGATATTAAAGTGGTCTCAGAAGTTAAAGTCACTTAAAGGTCCCATGAAGTGCTTGAAATGTGCAGTTTTTGTTTGATGCTTGATGTAATCTCTATTTTGACGATCCATGTGCAAAGTACAAACGTATTAAGGGCGTGTTAGAAAGCAAATTTGCTATTTTAAGGACGGAAAAATCCGCTTTGCGCAGTGGCGCATGATCTAATACGGTTGAGCTTATTCTCTTAATGAGTTATAGGTGTTTTGAGAATAAACCAATCAGAGTCTCATCTCCCATTCCCTTTAAGAGTTGTGTCGCGCTAAAGCGCATTTGCTATTTACATGACGGACTTTGTAAGTGGAAAAACTGAGCGTTTCACTAGCAAGAAAGCAGTTAAAAAGAGCATCTGCAGCGCAAGAATGAGAGTTGAGCCTCCTTATTATCTACTTTCACTTTCACTTTCGTGGATAGGGAAATCTTGCACGCCTTGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17642
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000012531 | Essential Splice Site | 338 | 494 | 10 | 14 |
ENSDART00000098384 | None | None | 155 | None | 3 |
ENSDART00000012531 | Essential Splice Site | 338 | 494 | 10 | 14 |
ENSDART00000098384 | None | None | 155 | None | 3 |
Genomic Location (Zv9):
Chromosome 2 (position 3082268)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 4554421 |
GRCz11 | 2 | 4395046 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGTCTCTAAACCCCTGCTCAGCTCYGCATCKCTCTCTTCACAACCAAAGG[T/G]CAGTAGCAGAGGTCAATGGGTCATTTTCAAAGATATTAAAGTGGTCTCAG
Long Flanking Sequence:
GATCGGTGCATCTTTACAATTTGTATTACAAAAAAATACAGTGTTTATTTTTTTATACACCTCCAAACCTAGGTCACGGACATGCTAAACTCTTCTAGATGAAGTCTCTTAACTTTATTTTACACTTGACAATTTAGACTTCAGATTGTTCTTCATTTAGTTAAAAGTGTGCTGTGTTTAGAGTTAATTTTGTACATTTGTGGTAAATTACAGCCATCCAAACCTGGCGTGTTCACACAAGACTTTTTTGTACTTGATCTTCTCACACCAGAGTTCTGTATGTTGTATTGTTGTTATTTAAACGTGTGATTATGTGTACGATTATTTTCTAACCGTGTGTTTGTGCTGACCAGCTCAACAGTCCGGTCAGTCACCCATGTCATTAGCATCAGACGCCTCTTCACCGAGGTCATACGTGTCTCCTAGAGTCAGCACACCTCAGACCAATGCCGTCTCTAAACCCCTGCTCAGCTCCGCATCGCTCTCTTCACAACCAAAGG[T/G]CAGTAGCAGAGGTCAATGGGTCATTTTCAAAGATATTAAAGTGGTCTCAGAAGTTAAAGTCACTTAAAGGTCCCATGAAGTGCTTGAAATGTGCAGTTTTTGTTTGATGCTTGATGTAATCTCTATTTTGACGATCCATGTGCAAAGTACAAACGTATTAAGGGCGTGTTAGAAAGCAAATTTGCTATTTTAAGGACGGAAAAATCCGCTTTGCGCAGTGGCGCATGATCTAATACGGTTGAGCTTATTCTCTTAATGAGTTATAGGTGTTTTGAGAATAAACCAATCAGAGTCTCATCTCCCATTCCCTTTAAGAGTTGTGTCGCGCTAAAGCGCATTTGCTATTTACATGACGGACTTTGTAAGTGGAAAAACTGAGCGTTTCACTAGCAAGAAAGCAGTTAAAAAGAGCATCTGCAGCGCAAGAATGAGAGTTGAGCCTCCTTATTATCTACTTTCACTTTCACTTTCGTGGATAGGGAAATCTTGCACGCCTTGGG
Associated Phenotype:
Not determined