ZMP
si:dkey-174n5.3
Ensembl ID:
ZFIN ID:
Human Orthologue:
WWC1
Human Description:
WW and C2 domain containing 1 [Source:HGNC Symbol;Acc:29435]
Mouse Orthologue:
Wwc1
Mouse Description:
WW, C2 and coiled-coil domain containing 1 Gene [Source:MGI Symbol;Acc:MGI:2388637]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa15129 | Nonsense | Available for shipment | Available now |
sa24002 | Nonsense | Available for shipment | Available now |
sa14794 | Essential Splice Site | Available for shipment | Available now |
sa12581 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa15129
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113678 | Nonsense | 63 | 1112 | 2 | 22 |
ENSDART00000138129 | Nonsense | 63 | 1129 | 2 | 22 |
Genomic Location (Zv9):
Chromosome 21 (position 35867594)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 36860842 |
GRCz11 | 21 | 36546022 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTGCYGACTGTATTGGAGATGAGCTGCCTGTGGGATGGGAGGAGGCCTA[C/A]GACCCCCAYGTCGGAGCCTATTATGTCGACCACAACACCAGTAAGTTAAG
Long Flanking Sequence:
ATTTTAGCATTATCTTTGCTATATTGTATGGATGTTGTTTTGTATTTTGCTTGTAGAGTTTATTTTATTCTTATATGACAGCACTTTTTTACTGAACATGTCATATACTGAACCGCACCGAAACCATGAGAAGTTTATATTGTTGCACCTCTAATCCATACTAAGAATATCCTGGAACATCCATACGAAACGTAAATGGAATATTCTAAAAGCAACTCATGTAATCACTTTATTCAAAATATAAATTATTATTATATAGTATTATTCAGAATAAGGTAAATAGTTTGATTACTGATGTGCATTTCATTTATACACAGCTACTGTGTGACATCCAGCAGAAAACAGGCATAAAGGTTGCAGGTGCAACAACACGCCGGCTTCTCTCTGATTGGTGGTTGACTGACAGTTGGATTGTCTTCTTGATTTTGCAGGCAGACTAAGCCTCTGACTTTTGCCGACTGTATTGGAGATGAGCTGCCTGTGGGATGGGAGGAGGCCTA[C/A]GACCCCCACGTCGGAGCCTATTATGTCGACCACAACACCAGTAAGTTAAGAAAGATGCGGACCACCTTATGGATAATTGGAATATAGCATGTCTTCTTTTTGATTCTCAGATAAAATGACATATCACATCTGACACAAATAATGGCTGGATTAAAGTTCAGTCAGTAGGCCTTATTCTAACTTAAATACACTTCTGTGTCAATTATTTTGTGCTGATGTCCAGTGTTTTTTAAATTATTTGATTTTATTTATCCGATTTTACATTTTTTTATTAAAGTTTATTTATTAATCTATTTAATTTTATTTTGTTTTATTAAATTCTATTTAATTATTGTATTTTTTATTTTATAAAATTTGCACGTTTATTACATCTAATTTAATAAATTTTTTTATTTCATTGCATCTATTTATCTATTTATTTTATTTAGTTTTATAAAATTTTATTTAACTACATTATTACTTTATTTTCTATTTTATTTTAATACATTTTATTACATTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24002
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113678 | Nonsense | 178 | 1112 | 5 | 22 |
ENSDART00000138129 | Nonsense | 178 | 1129 | 5 | 22 |
Genomic Location (Zv9):
Chromosome 21 (position 35860313)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 36853561 |
GRCz11 | 21 | 36538741 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTCTCTCTGTTGCTGTCTTTTGTTCAGGTAAATAAGCTGAAGAGAGATT[T/A]GGCCTATATGAAGCAAGAACTGCATTATAAGGAGCAAGGCTTTGAGACGT
Long Flanking Sequence:
CAGCAATGATCTCACTCTTCAAGCATTTGTGCAAGCAAAAACTCTTTATTTCGAATGAAACCTCATTATAATGGATGTAGATTTGTGACACAATTCTGTCGCGTTATTATACATCAGTGTGGAATTCAAAAGCTACGCCAAGTGGTTATACAGATAAGATAAAGCCTTTGAACTCTTATCTTCCCTACAGTAAATTCCAGATCCTCATCAAGCAGTAAATATGACCCTGAAATCCTCAAAGCAGAGATTGTTACAGCAAAAAGCCGGGTAAGAAGCTCTTCTACATATCACAAGCCTTTTATCGTTCGCTGTGAATGTTATCTTGTTTATGCAAGACACCAATTGGGTGTAAATTTTGCTGCAAGGATTTGGGACGTGATGACAGGCAGCGAGATTACGCTTAAAACCCAAATGTAATTACACAAGTGTCTCATTGATTCATCCGCTGGCTTTCTCTCTGTTGCTGTCTTTTGTTCAGGTAAATAAGCTGAAGAGAGATT[T/A]GGCCTATATGAAGCAAGAACTGCATTATAAGGAGCAAGGCTTTGAGACGTTGAAAGAGTAAGTGTAACCTGACCTATATTGCACGATCACGTTCCAGACAACCGATCGCTTCCTTGTTCAAATGCATTCCAGTCTGAAAACACCTCACCTTTGTGCAAGACAAAAAAACCTATCAACTTATCTCTTGGCATTTTATGAGCTCACTGGCATTTTATTGTGATGGAGCAAGTTGATGTTGACAAGTCTGTTGTTGTAAAAATGGATATTTTTACTGTTATAGAGCACCACATGCACCTCAGTGTAAATCTATTTATGGTTCATATTTGTTACTCTTAAAACTCTTAAATATTTGTTACTTTGAAAACTCTTAAATATTTGTTACTCTTAAATATTTGTTACTCTTAAAACTCTTAAATATTTGTTACTCTTAAAACTTAAATATTTGTTACTCTTAAAACTTAAATATTTGTTACTCTGAAAACTCTTAAATATTTTTTACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14794
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113678 | Essential Splice Site | 197 | 1112 | 5 | 22 |
ENSDART00000138129 | Essential Splice Site | 197 | 1129 | 5 | 22 |
Genomic Location (Zv9):
Chromosome 21 (position 35860254)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 36853502 |
GRCz11 | 21 | 36538682 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGAAGCAAGAACTGCAKTATAAGGAGCAAGGCTTTGAGACGTTGAAAGAG[T/C]AAGTGTAACCTGACCTAWATTGCACGATCACGTTCCAGACAACCGATCGC
Long Flanking Sequence:
ACCTCATTATAATGGATGTAGATTTGTGACACAATTCTGTCGCGTTATTATACATCAGTGTGGAATTCAAAAGCTACGCCAAGTGGTTATACAGATAAGATAAAGCCTTTGAACTCTTATCTTCCCTACAGTAAATTCCAGATCCTCATCAAGCAGTAAATATGACCCTGAAATCCTCAAAGCAGAGATTGTTACAGCAAAAAGCCGGGTAAGAAGCTCTTCTACATATCACAAGCCTTTTATCGTTCGCTGTGAATGTTATCTTGTTTATGCAAGACACCAATTGGGTGTAAATTTTGCTGCAAGGATTTGGGACGTGATGACAGGCAGCGAGATTACGCTTAAAACCCAAATGTAATTACACAAGTGTCTCATTGATTCATCCGCTGGCTTTCTCTCTGTTGCTGTCTTTTGTTCAGGTAAATAAGCTGAAGAGAGATTTGGCCTATATGAAGCAAGAACTGCATTATAAGGAGCAAGGCTTTGAGACGTTGAAAGAG[T/C]AAGTGTAACCTGACCTATATTGCACGATCACGTTCCAGACAACCGATCGCTTCCTTGTTCAAATGCATTCCAGTCTGAAAACACCTCACCTTTGTGCAAGACAAAAAAACCTATCAACTTATCTCTTGGCATTTTATGAGCTCACTGGCATTTTATTGTGATGGAGCAAGTTGATGTTGACAAGTCTGTTGTTGTAAAAATGGATATTTTTACTGTTATAGAGCACCACATGCACCTCAGTGTAAATCTATTTATGGTTCATATTTGTTACTCTTAAAACTCTTAAATATTTGTTACTTTGAAAACTCTTAAATATTTGTTACTCTTAAATATTTGTTACTCTTAAAACTCTTAAATATTTGTTACTCTTAAAACTTAAATATTTGTTACTCTTAAAACTTAAATATTTGTTACTCTGAAAACTCTTAAATATTTTTTACTCTTAAAACTCTTAAATATTTGTTACTCTAAAAACTCTTAAATATTTGTTACTCTTAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12581
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113678 | Essential Splice Site | 819 | 1112 | 15 | 22 |
ENSDART00000138129 | Essential Splice Site | 807 | 1129 | 15 | 22 |
Genomic Location (Zv9):
Chromosome 21 (position 35807940)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 36801188 |
GRCz11 | 21 | 36486368 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AATGGATGGAAAGCAAAAAGAAACWGAGATGCCCGCTCTGCAGGARCTGG[T/A]AAAGTATTAACACAAATACACACTCCTCAATTCACTTTACTTCACCACAG
Long Flanking Sequence:
AAGGTCAGTATTTTTAGCCCCTTTAAGCAAGTTTTTTTGGTAGTCTACAAAAGAGACTATAGCTATACAATGACTTGCCTAATTACCCTAACTTGCCTAATTAACCTAGTTAAGCCTTTGAAAAATATCTAGTTAAATATTATTAACTGTCATCATGGCAAGATAAAATAAATCAGTCAATAGAGATGAGTTATTAAGACTATTATGTTTAGAAATATGTTGAAAAAAATCTTCTCTCCATTAAACAGAAATTGGGGGGGAAATATAAAAGGAGGCTAATATTTCTGACTTCAACTGTAAATACAGGCCTAGATCAAAATAAATCTGATCATTTTTTTTTTTATTTTGCTCTTGAAAGGCTGGTGCTCAGATCAGCTTGGCTGATGAGGAGTATTCAGAGGAATGGTGCACCAAGTGGTACAACCTTCTCAACTGCACGTACATGCCAGAAATGGATGGAAAGCAAAAAGAAACAGAGATGCCCGCTCTGCAGGAGCTGG[T/A]AAAGTATTAACACAAATACACACTCCTCAATTCACTTTACTTCACCACAGCCGAATGCCTTGCTAACGATTCTTAGAAACAGTCTTGCCATACTGCTAAGCCTGTCGAGGAACAAGAAGTCTTCATTCATATTATATTCAGTTTTTGCGTCATTCAGATGAAGCAATGGATTCTTTCCTGGCCAAGCAGCCTTTCCGGCTTTCTAATGCTGTTAATAATTGAATTATGTAGAATTAGCTGCTTTGCTTCTTATCAGCAGTTTTGATTGTACAAACAAGCTGTTCTGTCCAGACGAATTAAAGGAATGTCCATTTTACATCTCCTTTCTAAGAATAATGCACAAAATAATGCCTGAAGCTGTTCTAAGATTTTTCATTTTCTGGCATTAAAATTGAAATAATCAATAACGTTACATATATGAAGTGTCTAAAGTAGGGCTGTGTAATTAACTAATTAATCACACTTTTTTTCTAATTAATCATGATTAATCGCGAAAAGCA
Associated Phenotype:
Not determined