ZMP
si:dkey-9k8.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein (Wu:fd18f09) [Source:UniProtKB/TrEMBL;Acc:B8A4V0]
Human Orthologue:
CASC5
Human Description:
cancer susceptibility candidate 5 [Source:HGNC Symbol;Acc:24054]
Mouse Orthologue:
Casc5
Mouse Description:
cancer susceptibility candidate 5 Gene [Source:MGI Symbol;Acc:MGI:1923714]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa17976 | Nonsense | Available for shipment | Available now |
| sa19442 | Nonsense | Available for shipment | Available now |
| sa32611 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa12744 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa17976
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 |
|---|---|---|---|---|---|
| ENSDART00000102929 | Nonsense | 1195 | 1824 | 9 | 25 |
| ENSDART00000147648 | Nonsense | 1165 | 1794 | 7 | 23 |
Genomic Location (Zv9):
Chromosome 1 (position 10284055)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 10416393 |
| GRCz11 | 1 | 11100504 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CMTTTTCCTCAAGGATGTCAYTGTGTGGGGYTRTTCCAAAGCTACCAAAA[C/T]GARCTACAGCTTTCACTCCCAACAAATCCCTGCCCATAAGTWTAAATGRT
Long Flanking Sequence:
TACCCGATATGCAAGTGGACAAAAATTGTGAAACGGCTCTCCCAAGCAATGTGATGGCGAACGATGAAGATGATATGCAAGTCACAAAGCCCCTAACATTGCCTATTGAAATTGAGCAAACGTTTTCATTTAACCAGAACGAAGAACCCAATACATCCTCCGGTTTTAGAAATGACAAAGAGGGTCATGCTCATAATGCTAAAGCAAGACGAAGAAGTTTAGCAGACTTTCAAATGGAGCTTCATAACATGTCACAACGTATCCTCGAAGAGCCAAATTTAATGACAGTAAGCGCAACTGCGCCTCTGCCTTCTTGCACACTCTCAGAGAACGTGCAGAATGAAATGGGAAGTTCTGCCGAGCCTGCTTCAAATGTCACACCTGTTGTCAAGCAGAAAAATAATTCTGCGCAAAGTCAGAAGACCACACCTTTTAGTCTTAACAAAAAATCCTTTTCCTCAAGGATGTCATTGTGTGGGGTTGTTCCAAAGCTACCAAAA[C/T]GAGCTACAGCTTTCACTCCCAACAAATCCCTGCCCATAAGTTTAAATGGTTTACCGTGTCTCGAGCTAGAGAAACATTTTGAAGTTGCTGAACAAAAAAGCAATCAAACAGTCGATATTAACGATGAAGAGTTCCCTGAAATGAGCAGTGAAGAAGACCTCTCGGGGAGTCTTGAAAATTGGCCAGTTAGTAAGCAAGATGAACTGGATGAATCTTTGGCTGTACCCATGAAAGAAGAGTTTTTAATAGACGATGTCTTCGAGTCAGGCACAAGCCCTTCTTTTAAAAGGCCACATCCAGAGGAAGAACCTATTACACCAGAACAAACCAAGAAGACCTGTGTTTCTGACATGGTAGGCACAAATGTTAATAATTTTCAGTTTAATAGTTTGTTTGCTTGGTGTTTCCTGCTACACACTTAGAGGTTGTTCTGTAATAAAGTGTTAAGCGTGGGCTCCATTGTTGTGCATTATTATGCTAATGGCTGAGATTCTGTCTCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19442
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 |
|---|---|---|---|---|---|
| ENSDART00000102929 | Nonsense | 1303 | 1824 | 9 | 25 |
| ENSDART00000147648 | Nonsense | 1273 | 1794 | 7 | 23 |
Genomic Location (Zv9):
Chromosome 1 (position 10283731)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 10416069 |
| GRCz11 | 1 | 11100180 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCCTTCTTTTAAAAGGCCACATCCAGAGGAAGAACCTATTACACCAGAA[C/T]AAACCAAGAAGACCTGTGTTTCTGACATGGTAGGCACAAATGTTAATAAT
Long Flanking Sequence:
CAGAGAACGTGCAGAATGAAATGGGAAGTTCTGCCGAGCCTGCTTCAAATGTCACACCTGTTGTCAAGCAGAAAAATAATTCTGCGCAAAGTCAGAAGACCACACCTTTTAGTCTTAACAAAAAATCCTTTTCCTCAAGGATGTCATTGTGTGGGGTTGTTCCAAAGCTACCAAAACGAGCTACAGCTTTCACTCCCAACAAATCCCTGCCCATAAGTTTAAATGGTTTACCGTGTCTCGAGCTAGAGAAACATTTTGAAGTTGCTGAACAAAAAAGCAATCAAACAGTCGATATTAACGATGAAGAGTTCCCTGAAATGAGCAGTGAAGAAGACCTCTCGGGGAGTCTTGAAAATTGGCCAGTTAGTAAGCAAGATGAACTGGATGAATCTTTGGCTGTACCCATGAAAGAAGAGTTTTTAATAGACGATGTCTTCGAGTCAGGCACAAGCCCTTCTTTTAAAAGGCCACATCCAGAGGAAGAACCTATTACACCAGAA[C/T]AAACCAAGAAGACCTGTGTTTCTGACATGGTAGGCACAAATGTTAATAATTTTCAGTTTAATAGTTTGTTTGCTTGGTGTTTCCTGCTACACACTTAGAGGTTGTTCTGTAATAAAGTGTTAAGCGTGGGCTCCATTGTTGTGCATTATTATGCTAATGGCTGAGATTCTGTCTCCTCAGGGGTCTGACTGTCATGAAGCTGCCGTACAGTGGGAAGGTAATTTTACAAGGCATGCCGCTCAGAATCCCAAGGCAAAGACAATTGAAGATACAGGAGTCTCTGAATCCAGTGAGTTGCGTATGTTAGTGCTCAGACACAGTGGAATGTTTATGCAAAACCATTAAGAAGATTTCAGTGTGGTTTATCTCTAAAAGAAAATGTGGTCTGCTTTCAGCTCTCAGGCACTCGCAGTTTGACTCTCATATGGACGGCATGCAGGATAATCTATTTGATTTTAATAAGGTAGCAATATACACAAACACTCACATTAATAGCTTCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32611
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000102929 | Nonsense | 1447 | 1824 | 14 | 25 |
| ENSDART00000147648 | Nonsense | 1417 | 1794 | 12 | 23 |
Genomic Location (Zv9):
Chromosome 1 (position 10280775)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 10413113 |
| GRCz11 | 1 | 11097224 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATAATATGTAATATATTTTATGGAACCTATTTTCTCATAGACTTAAAGAA[C/T]AAATGTCTGCACAAGAGAAATCCCTGAGAAGCATCAATGGAGCCCTTCAA
Long Flanking Sequence:
AATCATTTGCATATTTTGCATGGGCAAGCACCACTTACACTCTCTCCTTAAAATGTAAAATATAGTTGTTTATCTCAATGTTTTATTTCTAGAAACTTGAGGACGGAAGCATCACAGTGAACGAGTTTCTTAGCCACTTTGGCATCAAATTCGTCATCCACAGATCTAGACCAAGTGCTCTGCCTGTCAGGGTAAGTGGTCTAGATTATTCTTGCTCTCTTTATAAACATAAAAAGTAAAGGTTGTAACTCATCTTTCTTCTTTCAGTGTGGCGCTGGTGAGACACGCACCATCGAAGATTTGCTGAAAGAAAAATACATAAGCCACCCCAAGCAGAGAGTATATGAGCAAGACTGTAAGAACATTACAGAAATAGTGGAGAGGTGCGTGTCAGTCTGGCTTTGATAATGCTGTAAGATATTTATGTGTGCGTCTGTGTTTAACTTACTAATAATATGTAATATATTTTATGGAACCTATTTTCTCATAGACTTAAAGAA[C/T]AAATGTCTGCACAAGAGAAATCCCTGAGAAGCATCAATGGAGCCCTTCAACAAGAGATATGTACTCTCTCTGAAGAACAGGTATGTTGTTTTCATGGTCAGTCCTGGGTCATATTATGTTAAATCATTAAATAATTCATATATCATTCAACTTTTATATCAAGCCTGCATTTTTGTTAATTTTTCTCAGTTAAAAAGCTTTGGATCCAAGTTGAAGGAGCGAAGGGCTTATTTTGGGAAGAAAAGCAAAGCAGTTTCTCATGAAATGAAAGGAGTGTTGTACTCTGAGCTCATAAAAACAACACAGGTAAAGGACTTTTTTCTAACCTTTATTTATAAATTAGTCTACATATTTTTAAATAGTGTGAAAAAGTTTTAAGGCATAACAAATATTGAATGAAATCCATCTTTCGAATACTGCCTTTCAAGCCCCCTAAACTATGAAATTCTGTTTTCTATCATCTGTTTTGAGACTCATCATGACTCCAGTGATGCTGCTAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12744
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 |
|---|---|---|---|---|---|
| ENSDART00000102929 | Essential Splice Site | 1570 | 1824 | 17 | 25 |
| ENSDART00000147648 | Essential Splice Site | 1540 | 1794 | 15 | 23 |
Genomic Location (Zv9):
Chromosome 1 (position 10277801)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 10410139 |
| GRCz11 | 1 | 11094250 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGTCTTGATCTWCCTCAAGCAGGACCAGCCTTAAAAGCCAAGGAAGAAGG[T/C]AAGTTAAGTTMTATATAACCGATTTTTATGAAGCTATTAAGGAWAATGTA
Long Flanking Sequence:
ATTAATCTATAGTTATAAAACTACATACCCAATTAACTGCTGCTTGTATTTGATTAGACATACTGTATTTTCCCAGAAGTTAAGATTGTATAAATTGTAATTTAATTTTTGCAAATAGATTTTTGTGAACTTATAATGGTGTAAAAGGAGCACACTAGCCTATAGATGGCCTTGGTGGACTAAAAGCCTTAACTGATGTGGGTCTGTATTTTCCCCAATACATTTAGGATGCAAAACTGAGCCTGATATCTAAAATCAAAGAGACAGATGAAATGATTGAAGACTTGGATGGCTGCATTAAAGATTTAGAAACCGGTATGGATTTTCTGCTCTGCTCTGTTGCATGTCTGAATGTGTAGAACATAAAATACAAAATAATCTCATGGTTAAAGAATCCAACTCTACTTCAAAACAGATCTTGCGTCAGTTGATGCCATGATCACAGGGGATCGTCTTGATCTTCCTCAAGCAGGACCAGCCTTAAAAGCCAAGGAAGAAGG[T/C]AAGTTAAGTTCTATATAACCGATTTTTATGAAGCTATTAAGGAAAATGTAATTTTTTACTTCTCTGTACTGACAGATTTGCATCGACTCAATTCAGCTGTCACTTTCAAAGAGAGGTATGTACTTCTATTAGCACTATTATGTATGTTTAATATACACTTACTAGCCATTTTATTAGATACACCTTACTAGTACCAGGTTGGAGCCTCTTTTGCCTTCCGAACTGCCTTAATCTTTTGTGGCATAGATTTAACAAGGTACTGGAAATATTTCTCAGAGATTTTGGTCCATATTGACATGATAGCATCACATGGTTGCTGTGGATTTGTCGGCTTCACATCCATGATGCAAATCTTCCATTTCACCACATCCTGAAGGTGCTCTATTAAATGAATACAGTGAACTCATTGTCATGTTCAAAATACCAGTCTGAGATGAATCGCGCTTTATCCACGCTTTATTAAAGAAGTAGCCATCAGAAGGTACACTGTGGACATAAAG
Associated Phenotype:
Not determined