ZMP
wscd2
Ensembl ID:
ZFIN ID:
Description:
WSC domain-containing protein 2 [Source:UniProtKB/Swiss-Prot;Acc:A2BGL3]
Human Orthologue:
WSCD2
Human Description:
WSC domain containing 2 [Source:HGNC Symbol;Acc:29117]
Mouse Orthologue:
Wscd2
Mouse Description:
WSC domain containing 2 Gene [Source:MGI Symbol;Acc:MGI:2445030]
Alleles
There are 6 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa18797 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa9102 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa20380 | Nonsense | Available for shipment | Available now |
| sa40395 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa1167 | Nonsense | Confirmed mutation in F2 line | Not yet available |
| sa25294 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa18797
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 |
|---|---|---|---|---|---|
| ENSDART00000088639 | Nonsense | 11 | 572 | 1 | 8 |
| ENSDART00000088639 | Nonsense | 11 | 572 | 1 | 8 |
Genomic Location (Zv9):
Chromosome 5 (position 22461596)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 20174468 |
| GRCz11 | 5 | 20678268 |
KASP Assay ID:
2259-5650.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGGCTCGAGAGCCCATCATGGCCAGATCTCTGCTGAAGATCCACCGCTA[T/A]TTTCGGCGTAAACCGGTGCGCTTTTTCTCCTTCATCCTGCTCTACCTCAC
Long Flanking Sequence:
ATCACATTCAGATACAGTGCTTTTGTTTGCTCAGGGGCCTCATCAGTATTTCCTCCTTGTTCAGTAGCTGTCATTTTGTGTTTTTCAGTCTGTGAGTGAAGGCTGAGTCAGGCATGAATCAGCGCTGCTTTTAATTGACGGACAGCTTGGTGGGAAACAAGGTCTCGGGAGAGCGGGAGTCCGATAACAGGAGTGAAAGCAAGATCATCTTTCAGTCTTCAGTGCCACTCGCCTTTCACAACATGGCCTCTCTGGTGGCACCAATCTCCTCTTTTGGGACGTAGAAAGACTCAAGGACGCACAGGACAGAACTTGGTGTCGTTGCCTTAACAAGTCCCGTCTCCTGGATTTGCTATAGTTCTTGAAACAGACACTAAACAATGAACATTTTTTAGAAAGGTGCAGTCTCTGATTTTATATGTGTCTGTGTAACATCGAGGGCCAATGTGTGTGGCTCGAGAGCCCATCATGGCCAGATCTCTGCTGAAGATCCACCGCTA[T/A]TTTCGGCGTAAACCGGTGCGCTTTTTCTCCTTCATCCTGCTCTACCTCACTGCCGGCAGCCTTGTTTTTCTCCACTCCGGCTTCTCCAGCGATTCTTCTACCGCCGGCATCGCTGGAAGCGGCAGCGACCCACTTCTGTCTGAGGGTAGAGGAGGTACAGGTGGTGGGAGCGCCACGTCTGAGGGTCTGGGGCTCTTAGGTCGGGTGTTTAAAGAGACACGGAGAACCCCCCGGAGATTCGGACCACCGTGGATGAAGGAGAGTAGGGGGCAGGATGCACCCGAGTGGGCCGGACGAGGATTTGATCACACCAGCAGCTGGAGCCATGGAGCCAAAGGACGAACCACCAAAGAGATGGATGATGGGAGAGGTAAGAGCATTTCCTGCATTCTGTTTGTTTCATCTTTGAAATTGGTGTTAACCAAAGTTCATTGGTCAAAACAACAGCATTGAATGAAGTTCCATACTAGTCCAGCCTGGTTAATACTGCCGTTCACAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9102
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 |
|---|---|---|---|---|---|
| ENSDART00000088639 | Nonsense | 11 | 572 | 1 | 8 |
| ENSDART00000088639 | Nonsense | 11 | 572 | 1 | 8 |
Genomic Location (Zv9):
Chromosome 5 (position 22461596)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 20174468 |
| GRCz11 | 5 | 20678268 |
KASP Assay ID:
2259-5650.1 (used for ordering genotyping assays)
KASP Sequence:
GTGGCTCGAGAGCCCATCATGGCCAGATCTCTGCTGAAGATCCACCGCTA[T/A]TTTCGGCGTAAACCGGTGCGCTTTTTCTCCTTCATCCTGCTCTACCTCAC
Long Flanking Sequence:
ATCACATTCAGATACAGTGCTTTTGTTTGCTCAGGGGCCTCATCAGTATTTCCTCCTTGTTCAGTAGCTGTCATTTTGTGTTTTTCAGTCTGTGAGTGAAGGCTGAGTCAGGCATGAATCAGCGCTGCTTTTAATTGACGGACAGCTTGGTGGGAAACAAGGTCTCGGGAGAGCGGGAGTCCGATAACAGGAGTGAAAGCAAGATCATCTTTCAGTCTTCAGTGCCACTCGCCTTTCACAACATGGCCTCTCTGGTGGCACCAATCTCCTCTTTTGGGACGTAGAAAGACTCAAGGACGCACAGGACAGAACTTGGTGTCGTTGCCTTAACAAGTCCCGTCTCCTGGATTTGCTATAGTTCTTGAAACAGACACTAAACAATGAACATTTTTTAGAAAGGTGCAGTCTCTGATTTTATATGTGTCTGTGTAACATCGAGGGCCAATGTGTGTGGCTCGAGAGCCCATCATGGCCAGATCTCTGCTGAAGATCCACCGCTA[T/A]TTTCGGCGTAAACCGGTGCGCTTTTTCTCCTTCATCCTGCTCTACCTCACTGCCGGCAGCCTTGTTTTTCTCCACTCCGGCTTCTCCAGCGATTCTTCTACCGCCGGCATCGCTGGAAGCGGCAGCGACCCACTTCTGTCTGAGGGTAGAGGAGGTACAGGTGGTGGGAGCGCCACGTCTGAGGGTCTGGGGCTCTTAGGTCGGGTGTTTAAAGAGACACGGAGAACCCCCCGGAGATTCGGACCACCGTGGATGAAGGAGAGTAGGGGGCAGGATGCACCCGAGTGGGCCGGACGAGGATTTGATCACACCAGCAGCTGGAGCCATGGAGCCAAAGGACGAACCACCAAAGAGATGGATGATGGGAGAGGTAAGAGCATTTCCTGCATTCTGTTTGTTTCATCTTTGAAATTGGTGTTAACCAAAGTTCATTGGTCAAAACAACAGCATTGAATGAAGTTCCATACTAGTCCAGCCTGGTTAATACTGCCGTTCACAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20380
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 |
|---|---|---|---|---|---|
| ENSDART00000088639 | Nonsense | 110 | 572 | 1 | 8 |
Genomic Location (Zv9):
Chromosome 5 (position 22461301)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 20174173 |
| GRCz11 | 5 | 20677973 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACCGTGGATGAAGGAGAGTAGGGGGCAGGATGCACCCGAGTGGGCCGGA[C/T]GAGGATTTGATCACACCAGCAGCTGGAGCCATGGAGCCAAAGGACGAACC
Long Flanking Sequence:
GACGCACAGGACAGAACTTGGTGTCGTTGCCTTAACAAGTCCCGTCTCCTGGATTTGCTATAGTTCTTGAAACAGACACTAAACAATGAACATTTTTTAGAAAGGTGCAGTCTCTGATTTTATATGTGTCTGTGTAACATCGAGGGCCAATGTGTGTGGCTCGAGAGCCCATCATGGCCAGATCTCTGCTGAAGATCCACCGCTATTTTCGGCGTAAACCGGTGCGCTTTTTCTCCTTCATCCTGCTCTACCTCACTGCCGGCAGCCTTGTTTTTCTCCACTCCGGCTTCTCCAGCGATTCTTCTACCGCCGGCATCGCTGGAAGCGGCAGCGACCCACTTCTGTCTGAGGGTAGAGGAGGTACAGGTGGTGGGAGCGCCACGTCTGAGGGTCTGGGGCTCTTAGGTCGGGTGTTTAAAGAGACACGGAGAACCCCCCGGAGATTCGGACCACCGTGGATGAAGGAGAGTAGGGGGCAGGATGCACCCGAGTGGGCCGGA[C/T]GAGGATTTGATCACACCAGCAGCTGGAGCCATGGAGCCAAAGGACGAACCACCAAAGAGATGGATGATGGGAGAGGTAAGAGCATTTCCTGCATTCTGTTTGTTTCATCTTTGAAATTGGTGTTAACCAAAGTTCATTGGTCAAAACAACAGCATTGAATGAAGTTCCATACTAGTCCAGCCTGGTTAATACTGCCGTTCACAAACAAAATATGATTTGGTATAGGACTGGGCGATATTGCAAAAAAAAATTATCACAGTATCATGTTTCAAATCATTCAATATTGATAATTAATAAATATTTGTTAGCAATACATATAGGAATATTAGGATTTATTTTATTTAAACATTTTATTTCAGTTTACCAACATTACTAAGGCAAATAGTTTAAATAGTCAAAAACAAATTTTTTTAAACAAAGTATCTGATCACTTTATAATAAACAATCGCGTACGTGGAAACGCGTGCATGTAGATTCCTTGACCATTACAATGGACTCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40395
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 |
|---|---|---|---|---|---|
| ENSDART00000088639 | Nonsense | 177 | 572 | 3 | 8 |
Genomic Location (Zv9):
Chromosome 5 (position 22430870)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 20143742 |
| GRCz11 | 5 | 20647542 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCAAATGAATGATGATGTTGTTTTCTCTGTGTTTCAGGGGTTATCTTTA[T/A]GCTGGTCTCGAGTTTGGAGCCGAGTGCTACTGTGGCCATAAGATCCAGGC
Long Flanking Sequence:
ACTAGTTTCTCACAGGACACCTGTAGTCTCTCTCAGACATCACTAGTCTCTCGTAGGACACCACTAGTTGCTCTCAGACATCAATAGTCTCTCACAGGACACCACTAGTCTTTCTCAGACATCACTAGTCTATCACAGGACATTACTGGTTTCTCACAGGGCATCACTAGTTTCTCACAGGACACCTGTAGTCTCTCTCAGACATCACTAGTCTCTCGTAGGACACCACTAGTCGCTCTCAGACATCAATAGTCTCTCACAGGACACCACTAGTCTTTCTCAGACATCACTAGTCTCTCGCAGGACATTACTAGTTTCTCAAAGGGCGTCACTAGTCTCTCACAGGACACCACTAGTCTCTCTCAGACATCACGAGTCTCTTAACATTGTTGTTTTTCTTCATAAGCACCACGGTTCATCATTTTAAAGAACTGGACATCCAGATAATAAACCAAATGAATGATGATGTTGTTTTCTCTGTGTTTCAGGGGTTATCTTTA[T/A]GCTGGTCTCGAGTTTGGAGCCGAGTGCTACTGTGGCCATAAGATCCAGGCTCCCAATGTCTCAGAGAGTGAATGCAATATGGAATGTAAAGGGGAAAAGAGTAACCTTTGCGGTGGTCCTAATCGACTGTCCATATATAGACTGGAACTGAGCCAGGAGTCAGCCCGCCGATGTGAGTATCCTGAAACACACACGTTTCCAGATACGTTTAACGTTGATGTTAAGTTTGGGCTTATGGTATTTGCATTTCTACATGATTGTTATCCAACTCTTATTCCCCAGTTTACAGTTATGGTTGGGTTTAGGGGTAGGGAATAGGTATAGTTGATATTTCGAACAAAAATGATTTTCCAGGATCAACATAGATGTTATTACAGGATTGCATCGTAGAAAATCATGACGTGCTACTGCCTTTAGGTTGCTTGGGTAAAGTTTATAATGACATTCACTGACAGCGAATGAGTTTTCTTACCTCTGAAAATACACATTTAGAACACTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1167
Status:
Confirmed mutation in F2 line
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000088639 | Nonsense | 358 | 572 | 6 | 8 |
Genomic Location (Zv9):
Chromosome 5 (position 22417586)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 20130458 |
| GRCz11 | 5 | 20634258 |
KASP Assay ID:
554-1077.1 (used for ordering genotyping assays)
KASP Sequence:
GCTTTTTACCTACTCGTTCCAAGCACCTAATGGCACTAGCTAGTTTTCCC[G/T]GAGCGGGCAACACCTGGGCCCGTCACCTTATTGAGCTGGCCACRGGTTAC
Long Flanking Sequence:
AGTCAAAAGTATTAGCCCCTTTAAACTATATTTTCTTTTAATAGTCTACAGAACATGCCACTGTTATACAATAACTTGCTTAATTACCCTAATCTACCTAGTTAACCTAATTAACCTTAAGCCTTTAAATGTCACTTTAAGCTGTTTAGAAGTGTCTTAAAAAATATCTAGTCAAACATTATGTACTATCATCATGGCAAAAGATAAAAGAAATCAATTATTAGAAATAAATTATTAAAAATATTATGTTTAGAAATGTGTTGAAAAAAATATTTGCAGTTAAACAGAAATTGGGGAAAGAAATACACACAGGGGTCTAATAATTCAGTAAGGCTAATAATTCTGACTTCAACTATATATGTAATTCAATATCTTCATGTTTGGTCAATATGGTCTGATGTTTAGTTTGTGTTTTCTTTATCTCTACAGATAACCGATGTATGGATCGGCGCTTTTTACCTACTCGTTCCAAGCACCTAATGGCACTAGCTAGTTTTCCC[G/T]GAGCGGGCAACACCTGGGCCCGTCACCTTATTGAGCTGGCCACGGGTTACTACACCGGCAGTTACTATTTTGATGGCTCACTCTACAACAAAGGTCAACTACTCAAAAACTTTTTGGTTTTCTCAAAAGCCATCTATTGTCTCATGTTCACTCATGGTGGTTTGATCTCTCTGCATGTGCAGGTTTCAAAGGGGAGCGAGATCACTGGCGCAGTGGCAGGACTATATGCATCAAAACCCATGAGAGCGGCAAGAAGGAGATTGAGACTTTTGATGCCAGCATCCTCATGATCCGCAACCCTTATAAAGCCCTCATGGCGGAATTTAACAGAAAGTATGGCGGCCATATTGGATTTGCCTCACAAGCTCACTGGAGGGGAAAAGGTGAGAGATGAAAGCTTGTCCTAAAATCTAGTTATTGCACGTAATTAGTGTATTTTAGTTCTGAACAATTTCAGAAATAAATCAAATAGCATTATTTTTAACCAGTATTGCGATTAT
Associated Phenotype:
Normal
| Stage | Entity | Quality | Tag |
|---|---|---|---|
| Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa25294
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:
C > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000088639 | Nonsense | 386 | 572 | 6 | 8 |
Genomic Location (Zv9):
Chromosome 5 (position 22417500)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 20130372 |
| GRCz11 | 5 | 20634172 |
KASP Assay ID:
554-7774.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGGCCACGGGTTACTACACCGGCAGTTACTATTTTGATGGCTCACTCTA[C/A]AACAAAGGTCAACTACTCAAAAACTTTTTGGTTTTCTCAAAAGCCATCTA
Long Flanking Sequence:
CCCTAATCTACCTAGTTAACCTAATTAACCTTAAGCCTTTAAATGTCACTTTAAGCTGTTTAGAAGTGTCTTAAAAAATATCTAGTCAAACATTATGTACTATCATCATGGCAAAAGATAAAAGAAATCAATTATTAGAAATAAATTATTAAAAATATTATGTTTAGAAATGTGTTGAAAAAAATATTTGCAGTTAAACAGAAATTGGGGAAAGAAATACACACAGGGGTCTAATAATTCAGTAAGGCTAATAATTCTGACTTCAACTATATATGTAATTCAATATCTTCATGTTTGGTCAATATGGTCTGATGTTTAGTTTGTGTTTTCTTTATCTCTACAGATAACCGATGTATGGATCGGCGCTTTTTACCTACTCGTTCCAAGCACCTAATGGCACTAGCTAGTTTTCCCGGAGCGGGCAACACCTGGGCCCGTCACCTTATTGAGCTGGCCACGGGTTACTACACCGGCAGTTACTATTTTGATGGCTCACTCTA[C/A]AACAAAGGTCAACTACTCAAAAACTTTTTGGTTTTCTCAAAAGCCATCTATTGTCTCATGTTCACTCATGGTGGTTTGATCTCTCTGCATGTGCAGGTTTCAAAGGGGAGCGAGATCACTGGCGCAGTGGCAGGACTATATGCATCAAAACCCATGAGAGCGGCAAGAAGGAGATTGAGACTTTTGATGCCAGCATCCTCATGATCCGCAACCCTTATAAAGCCCTCATGGCGGAATTTAACAGAAAGTATGGCGGCCATATTGGATTTGCCTCACAAGCTCACTGGAGGGGAAAAGGTGAGAGATGAAAGCTTGTCCTAAAATCTAGTTATTGCACGTAATTAGTGTATTTTAGTTCTGAACAATTTCAGAAATAAATCAAATAGCATTATTTTTAACCAGTATTGCGATTATGAATATGTACTTTCTTCAAATCTCTTCTTTTTTATTTTAGGACTAACAGAAATCATTATAAAATAGCCAACAAAACATCAGTGTGT
Associated Phenotype:
Not determined