ZMP
zgc:158241
Ensembl ID:
ZFIN ID:
Description:
protein WWC3 [Source:RefSeq peptide;Acc:NP_001103940]
Human Orthologue:
WWC3
Human Description:
WWC family member 3 [Source:HGNC Symbol;Acc:29237]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa33885 | Essential Splice Site | Available for shipment | Available now |
sa40713 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa20721 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa33885
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:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000088142 | Essential Splice Site | 654 | 1148 | 12 | 23 |
Genomic Location (Zv9):
Chromosome 6 (position 30266771)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 30587687 |
GRCz11 | 6 | 30574601 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGGATGTTTTGGCAACAGACAGCGGGGTATTTGAAGCCTGGAGTAGAAG[G/T]TGAGATGCGAATTTACAGTTTACCAGAAATTCAATTCTGTCATCCATTCA
Long Flanking Sequence:
ATGTGCTGTGATTAGGGCTGTGATTGAAATATGTTAAATCTGTTAGTCCATTAATGCCTTTATGAAACAAAAGTTGCATTTTTAATTTATAAACATGGTAATTATAGAATATGGTTAATCGCAGGCTAGGAAAACGTGGAAGACATTTAATTTGTGTGAGAGATGCGTATTTGTTAAAAGGATTTCTTACAATGCAACAGATAATAGAAACAACACTTCTCAAAGCTTTGAATCAATTAAAGCAACTGCCTCACAAAATGATTTACAACTACTAAGATTCAGTTTAATATTATCATGTACACACCCATTTTATATTTTTATTTATACCCATTTCTCTTTTTTCTGTTTGTTTTGTGCATGTATATGTTACTCTATACAGGAGTGACCTTGCGCTGTAAAAGTGCAAGTCGGACCAGCAGAAGAGCAAGACGAGTGTCTGCAGGGGTAAATGAGGATGTTTTGGCAACAGACAGCGGGGTATTTGAAGCCTGGAGTAGAAG[G/T]TGAGATGCGAATTTACAGTTTACCAGAAATTCAATTCTGTCATCCATTCAATCACTCCTGTCATTCATAAACTGTGTTTTTTCTGTCATTCCATTGACCTGAAGGCCCACTTGCTTTGGAATGTGTCAAAAAAGTTTGTTCATATTTCCTGTACACAAACACAGATTAACATTCAAAAGTTGTTTTATGATATTATTGATTTTATTCTAGGAGGACAAATAGCTTAAAATAAAAGAGATGTCAACATTATTACAATTCGTTTTATAAGAACTGGGACTATAAGAACTATTTTTTTTCTTCATAAAGTTTAACATTAATATTAAATGAATAAACAAAACAAATACATCAATACACTACAAAGTGCAAAACTTAATAGATATTTGTACTAAAATCTAAACAGGCCTACAAACAAATTGCCTTAAAACCTTTTGGTGCAATCTACATAAACAACCTAAAGTGTATAGATGCATAAATGAAAATGCATCTTTTAATAAACAATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40713
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000088142 | Essential Splice Site | 712 | 1148 | 15 | 23 |
Genomic Location (Zv9):
Chromosome 6 (position 30268938)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 30589854 |
GRCz11 | 6 | 30576768 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTTTACACTTTACGCACATTTGTCATTATCTCCATGTTGCTCTCTCTCA[G/T]ATTTGTGAAGGTTCATGTTCTCCCGATGGACTCCAGTCGGCCCTGCACTT
Long Flanking Sequence:
TAGTAAGGTGTACCTAATAAAGTGGTCAGTGATTGTGTATGTTCTTTAATTAGGCACATCAAGCTGTGTTGTTATTATTATTATTATTGATCAGATTTTATGTCTTTTTCCAGCAGGACAGAAGAATCGGAAGAAGTCAGTTTTGCTCAGGACGTTACAGTTGCAGTCTCAGAGCCAGTTCATATTCAGATTGGCCTTCTGTAAGCATCACACACTCTCCAAAAAATCTGTATCATTTTTTTTTTACAGCTATTCATTTGTTCATTCATTCATTAATTAGCTGACTCTGGGTGTTTCTTTTACAGATATGATTCAAATAGCAGGTTTTTGCTGCTGCATGTTCTTCAAATGAGAAATTTAAGCAAGGCCAGCATTAGAGATAGATGGAAAGTGTAAGTATACTTATCTTAATATCAAATATTTCACTCATGTTCTTTTAATATTGCAGGTACTTTACACTTTACGCACATTTGTCATTATCTCCATGTTGCTCTCTCTCA[G/T]ATTTGTGAAGGTTCATGTTCTCCCGATGGACTCCAGTCGGCCCTGCACTTATTATTGCTGTAAGGCACAGGAGCCTCAGTCTCTGCTCAGCTTTAATGAGAGCTTCCGGATCCCACTGAGTGTTGGAGGCCCCGGGGCCCATGCCTTACAGTTCAGCCTCTGCACGCTTGGACCCCTGGCTCAGGAGGAGCTGCTGGTCAGACTAAAATTCACTCTGATTAAAATGAGGATAATGTTATCAATAAGACAATCTGCATTTGTTAGATGTGCTCTGTAAAAAAAAAAATTATTGTGCTCTGCATAAAGAAAAGAGTCTCAGCTTTCCATCGCTGTAAAACGTTACATTCACGTACCTTCGGAGGCTCCGGAATCAGTGTGGTTAAGTCATCACATTTTGACAACGCTGATTTGACAAAGGAATACTCGTGGCTTGTGTCTCCGGACAAACCAGACATGATGCATTGATATTTTGTCCCTCCTCCATGCTCAGATTGGTTCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20721
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000088142 | Nonsense | 1111 | 1148 | 22 | 23 |
Genomic Location (Zv9):
Chromosome 6 (position 30282665)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 30603581 |
GRCz11 | 6 | 30590495 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGAGGAGGCTGCTGAGAGGAGGTTGAGAAAGGCTTCAAAAGAGGTCTTA[C/T]AAATGAGGGGCCAGAGCCACAAAGAGCCCCTTCCTGTGCAGACATTCAAG
Long Flanking Sequence:
AAATAACTGTAAAAATCATTGTAGGGCATGTTCCTTTAAAAGAGTAATTAGTTATAGTTCCTAGTTACTTCTCACAAATAGTTACTGAGTTAGTAACTGAGTTACATAATTCTAAAAGTAACTATTGCATTACTTAAAATATATAAATAATTTGTCAAATGAATAAAATAAATATAAAACATTGTACAGAAATCTACACTGTTTGAATGTTGTTGTGGGCCAATGTGAGAGACAACCATCAAATTCAACATATCACTATGGATATTATAATTACTGTAGTTGCACAATAAAACACAATAGAGGGTTTAGAACTTTAAGTACTTATTGCACAGACCACAACTGTTAAGATTTGAGGTGCTTCATTAGATTAGAATTACTTGTCTGTGTTAATGTCTTTCTTTTGCTTTGTGTCTCGTGTGCAGTCGAAGCAGACGAGGCAGGAGCAAAGGCAGGAGGAGGCTGCTGAGAGGAGGTTGAGAAAGGCTTCAAAAGAGGTCTTA[C/T]AAATGAGGGGCCAGAGCCACAAAGAGCCCCTTCCTGTGCAGACATTCAAGTGAGTCCAGCAACTGTAAAGTGTTCATCGGTGTGTCTGCTGTTATGGACATCATTTTTACATTTGCTATTTATTAAAAAAGATCTACGACTAAAGCCTGGTTTATACTTCTGCGTCAAGAGACCGGTGTAACCATCGATGCATGCAACGCCCGTAGCTGTGCATTTATACTTCTCTGGCTGTCTCTGTTGGTCTGCATTACACTTCTGAAACGCTAGTTGGCAGTGAGGTGTAAATGTTCCTCTGTGTCGAGTTTCTTCACTGCTGTTTTGCTTTTCCAGAACACTTTCTGGATGTACTAGTGGCTCAAACTTGCTCATTTTAAGGCATGAACCGGCGGACGTGCAACAACTTTAACTGTGAGGTAAACACAAAACAAAACTTTCCATCAGCAGCCCCTTCAAGGAACTCCACACTTAAAAAACAATCGCTCCATTGGGCTTGCGCCCAG
Associated Phenotype:
Not determined