ZMP
si:dkeyp-67d2.5
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:B0S755]
Human Orthologue:
CCDC141
Human Description:
coiled-coil domain containing 141 [Source:HGNC Symbol;Acc:26821]
Mouse Orthologue:
Ccdc141
Mouse Description:
coiled-coil domain containing 141 Gene [Source:MGI Symbol;Acc:MGI:1919735]
Alleles
There are 7 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa11814 | Nonsense | Available for shipment | Available now |
| sa18522 | Nonsense | Available for shipment | Available now |
| sa15829 | Essential Splice Site | Available for shipment | Available now |
| sa41541 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa34749 | Nonsense | Available for shipment | Available now |
| sa947 | Nonsense | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa11814
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 |
|---|---|---|---|---|---|
| ENSDART00000109613 | Nonsense | 359 | 1696 | 7 | 26 |
| ENSDART00000134349 | None | None | 605 | None | 9 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 44191292)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 43316462 |
| GRCz11 | 9 | 43118249 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCCTCATGATGAGTAGACAGGCTCATCTGCAAGAGAGCAATRCTTTTTA[C/A]AGCAGCGCTAATAAAGTACGTAATCAAGYAGCACTTCACATACTTTGACT
Long Flanking Sequence:
GTTTCATTATGTTATGTTGTGCTATGGTATATTGTTTTGTTATGTTTTGTTTTGTTTCGTTATGTTTTGTTATGTTTTATATTTCATTATATTTCATTATGTTATGTTGTTTCATTATGTTTCAAATGTTTTACGTTTCATTGTTTTGTTATGTTATGTTTCATTATTTTATGTTATGTTATGTTGTGTTGTGTTGTGTTTTGTTATGTTTTGTTATGTTATGTAATAGTCAATACATCTATTATGCCAATAAACGTTTATACTATAACTCATTGGACACCTAAGTCACTTTAAATCACTGCACTGTGTTTCTTCCAACAGGACTGGGCTGTTCTGGTGGAGAAGTTACTAGAGCAGGCATCATATCTGCTTTCCTCAAATGAGTCCACACAACTTCAATGCTTGTCAGAGAAGAGTGAAAAACTCAGAGCATCACACCAGCAGTTCTGGAGCCTCATGATGAGTAGACAGGCTCATCTGCAAGAGAGCAATACTTTTTA[C/A]AGCAGCGCTAATAAAGTACGTAATCAAGTAGCACTTCACATACTTTGACTAAGTTGAGGTTTGGATAACTGAGCTGACAGAGTCCTTACTCTTGGTAAACACTCCAGCGGTCCTATTTCTTCTGACTGCACTCATGTGTCATATGTTTTCTGCTGTAGATAGTTCCCTCTGGTGGAGAAGTAGATGACTATAAAAGATGGTAGATTTATTTACTGTAAAGAGTTTTTGTACAATGATAAAAAGCTGTTAAGATATTTTAATGGGTTCTCTTTAGTATTTTATTTTATTTCAGAATGGAGGCTTTTAATTAAATAAGATATGAATACAAATGATACTTGAATTTTAAAGATGCTTGAATTTTGTTGTGTACTTTTAAAATATAGGATGCTGAGGCTCTAGCAAGAGCAAGATTGACTACAGACTGAGCATATTGTGAATTGTAATTTTTTTGAGTTAATTTATTTAGTTTATTTCTTACTAATTCATTGTGAGTTTTAGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18522
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 |
|---|---|---|---|---|---|
| ENSDART00000109613 | Nonsense | 506 | 1696 | 10 | 26 |
| ENSDART00000134349 | None | None | 605 | None | 9 |
Genomic Location (Zv9):
Chromosome 9 (position 44187314)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 43312484 |
| GRCz11 | 9 | 43114271 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATCTCTAACTGAGGCTGAAGACGCTCTGAACAAGCATGTTGAGCTGCTMT[C/A]ACAGTCTCAGGTGAATTCCTGCCCCTAGATRAGATTATAGTATGATACAG
Long Flanking Sequence:
TAGATATATTATTTATATATAGCCTTTACGCTTTATTGTTGTACCTAAGGGCATATATGAAAAGCTAAATATACTTTATATAATTTTGACATGTAATATTTACTTTTCATAGGACATTTTTTACATTGTAATAGACAAATGTACGAAAGATTATCACAAAAATAGCAAATGCTTTTTAATTTTTTTTCATCGCAATAAAGAACAAATCATGCTTGTTTATTCAATTAACCTTAATATGTTTTGCTGCGATTCTCTACAGTTATCTTTTTATTGCATCATTACATTGTTTCTCATACAGTATGTTGTGTGCTTTTATTATGGTAAGTTGTTGAAAAGGGCATATATTTCCATTTCATATATTATGTTTTATCTCAAACTGCTGAATCTTCAGATCTCGGCTTGGATAAAGAGCAGCAGCAGTGTCCTCTCCGCCAGCACAGAGCCCGGTTCATCTCTAACTGAGGCTGAAGACGCTCTGAACAAGCATGTTGAGCTGCTAT[C/A]ACAGTCTCAGGTGAATTCCTGCCCCTAGATGAGATTATAGTATGATACAGAAAAGTCAAAGCAAATTGTGCTGCAAACTAAGAGCTTCTCGTAGTAATATTTACATTATTAGACTTTGTTTTCTGCTCTGTTGACTTTGGATGTTGAAAATTTAACTGCAGTTTAGGGAATTTTATCGACATTTTAGTAGTTTGAAACACGATTTTGGTTGAATTGTGTGTAAAATAACTGAACAAAACTATATTGGCAGCTTTTTGTATGTAAGTTACAATACCAATCAGACAATATATCCCTTCAGGCTTTTAAATATAAAAAAAAGAGTTACTTTTTTTACATTTTCAACATTAAAAGCTGTTGGAGAAAAGATGAAGGTCTCATAATGCAATTTAAAAAACACGAATGCCAAAATACTGTTAGTTTACAGGTATTTTACAGTGCAAGCCATGTGTTTCTCTGAGCTGTGATTTTTGTCCTGCAGGACTTTATGAAAGAATCAGAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15829
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 |
|---|---|---|---|---|---|
| ENSDART00000109613 | Essential Splice Site | 798 | 1696 | 15 | 26 |
| ENSDART00000134349 | None | None | 605 | None | 9 |
Genomic Location (Zv9):
Chromosome 9 (position 44183374)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 43308544 |
| GRCz11 | 9 | 43110331 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGAAACTGTTCTCAGCATGGCCAGCAARTTTCATCAGCTTTATCAAGAGG[T/G]AAAGGCTCATTTCTGTCCAAMACTTTAGAGAATCAGTGTAAGCTTAGGCT
Long Flanking Sequence:
ATATCACATAATGTAAATGTGTTAGTTATTCGCTAGCTTTCAAAATTAATGCAAACATAATCAGTTAAACTTTGTTAATTCTCTGCAGGTTCATCATGATTTAAAGGCCATGGAGGATATTTTTGCTCCGGCATCAAAAATTGATTTGGGAGGTGATCCTCAGTCTGTGTTTAAACTTCAGGAAAAATTCACCTCTGTGAAGCCAGAATTCCTGGTTAGATGTGCATTTTATTTTAGTTATTCATTCATGGTTGTTTTCTTAATATTACTTTTTAATTCACTGCTAACTTCTATTTCAAATACCACATAGCAACTCAATGCAGAGGTGGAATTCCTGGTTAAGACATCTGAGCTGCTCAGCTTGAAAGGAGTACCTGCGAAAGAGAAGAACGAGAAAGTCTCAGAGCTTCTGCTGCTGCATCAGCGTATCAGAGATAAAATTAGAGAGTATGAAACTGTTCTCAGCATGGCCAGCAAATTTCATCAGCTTTATCAAGAGG[T/G]AAAGGCTCATTTCTGTCCAACACTTTAGAGAATCAGTGTAAGCTTAGGCTGAAAACAGACTGTAATGGATTTCTAAATCAGAATAACATAGAAGTCAGACACCTCTTTTTTTAATGATGGTTCTTAAATCGCATTCTTTAATATTGATATTCTCAGTTTTAGAGTAATAAATAACAAATGTAAGAAAATGAAACATTTGAAAGCATATTCAAAGGCACCAAACTTCTCATTTCCATCTATTTAATAAACCCTGTTAAACACAGTCACAAGCATCCTGACTACTATAAGGGTTCCCACGGGTCGAGGAATTCCTGGAATAACATAAAACTTTGTTAACAGATTTCATGTTGGATTTTGTATTTGTTTTATTGTTTATATTTTTTTGTTTGTTATTTGTTTTTAATGTTACTTTCCATAAGTCAAAATGTAATATTTCTATAACATATATGAAGTTTACAGAAGCTTCACCTTCTTGACATTATTGGCCTCAACTACAGGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41541
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000109613 | Nonsense | 998 | 1696 | 19 | 26 |
| ENSDART00000134349 | Nonsense | 182 | 605 | 4 | 9 |
Genomic Location (Zv9):
Chromosome 9 (position 44164951)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 43290121 |
| GRCz11 | 9 | 43091908 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTTAAATGAGCTGCAGAGACAGGTGGGCGACTTTGACAGGGCAGTGGAG[G/T]AGTACAAACAAAACCTGGACATGAATGTCAAGCTCCAGCAGGCTTTAGAG
Long Flanking Sequence:
CAGAACAAATCTTTTGTTTTCTTTTGCATGATTTGCCTTTAAAGTATTTAAACATTTATTTTTATTTTTATTTTTTTAGCTGAGGGAGTCCTTTAAAGATCTTAAAAAGAAGTTCAACAATCTGAAATTCAACTACATGAAGAAAAACGAAAAGTCAAGAAACTTCAAGGCGGTAAAAAATCAGATCCAGCAAATTGAGATATACATTGAAAAGCTACAGGTAATGAAACATATTAAATTATAAGTGTCTGTTGATTTTTTTTGTGTGACAAATCTTAGTTAATTATACACGCTGATACCTCAGGAAATGTCTTCCTCTGTCAATGTTTTGACAATCTATTTCTAAAATGTTTTAGCTTTTAAAGAAGAAGCTGCAGGCCTTCACTCTGAAAATGTCCAGCAGCAGTGAGAGACATTTAATTGGCAACAGCCTCAGAGAGATTGAGGATGCCTTAAATGAGCTGCAGAGACAGGTGGGCGACTTTGACAGGGCAGTGGAG[G/T]AGTACAAACAAAACCTGGACATGAATGTCAAGCTCCAGCAGGCTTTAGAGGAGGTGGGGTTCACCAGGAACACATAATTAGATAATACCAGCTACTAAAACAATTCAGCAGCAATTTGACACTCATTTTATAATCATGCTGTGGATTGTGTTTACTCATTTATTGCATTTAGCTTCCAATTTCGTTTTCTGCTTTCCTTTCATTGTTAATGCTGCTAAGAAAACAACATGATTATGACTTGCTTTCGCTTATGTATGACTTCAGAACAGCTATAAATAGTCTCTGAAAATAGTCTCTCCTCTCACCTTTCATTTTAAATGCAGTATCAGTTCTGGTGCGACGAGGCAAGCTCCACAATTGTGCGTGTGGGTAAATATTCCTCCCAGTGTAAGACTAAGGAAGCGGTCAGCTGTCTCTACAAACAGTTTGAAAAATTTGTGTGGCCCACAATCCCACAGCAAGAGGAGAGAATTAGCCAGATCACAGAGCTGGCAGTGCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34749
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 |
|---|---|---|---|---|---|
| ENSDART00000109613 | Nonsense | 1304 | 1696 | 23 | 26 |
| ENSDART00000134349 | Nonsense | 488 | 605 | 8 | 9 |
Genomic Location (Zv9):
Chromosome 9 (position 44161789)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 43286959 |
| GRCz11 | 9 | 43088746 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTATGGAAAAACCTTGCCCTGTTCAGAAGACCAGCTCTGAGGACAAGTAT[C/T]AGGCCTGTAATAGAAATCCCCCTTTACATTCATATTCCAAGGTGAGCCTG
Long Flanking Sequence:
AACAAAAGGAGAGTGGACATACCCCTGAGATGACAGGTCCACACTGCACTAAAGAGATGCCCGATGGCAAGAGTCCAGAAACCAAGAAACCTCAACTCCGCAAAACACGGAGCCAAGATCTGCCAGACAAACATCATACAGAGCATCAGAAAGTGTTGTCAGAGACTAGATCTTACACACAGGAAGCCTATTCCAAGACCAGCAAAGTGGAGACCATCACCAGCAAATCTACCATAGAGAAAAGAGAGGAAATGCACACATCTTTCTCTCACTCCCACACCATTAATGTGAGCCGTTCCCCTGTGCAGCGAGAGAAGAGGAGTCACTCTCTCATGCTAACAAAGAGAGACTCGCAAGAAACTCCTCCACCACCACCACCTCCTCCTCCTCCTCCACGAGATCCAGGTCTTTCTCGCCCCAGCATCATAAACATACAGAAAGAGTTACAGAGTATGGAAAAACCTTGCCCTGTTCAGAAGACCAGCTCTGAGGACAAGTAT[C/T]AGGCCTGTAATAGAAATCCCCCTTTACATTCATATTCCAAGGTGAGCCTGCTTTGACATTAGAGGCATTCTGTGAAACTGATCCCTTGTTAAATATTTTTAATTAAGAATGTAAACATACTAGGGCTGCACAATATATTGTAAAATTATTCAGCTAATGTCAAAATTAAATTTTAGTTAATGCATTTACTAACATTTATTGCAGTTTTTTCTCATGTTAGTTAATGTTGGTTAATAAAAATAGTTACTTATTGTTAGTTCATGTTAAGTCATGGTGCATTAACCAATATTAACAGGCATGAACTTAGAATTGCTGTACAACAGGGGTGGCCAATCCTGTTCCTGGAGAGCTACCTTCCTGCAGATTTCAGTTGCTACCCATATCAAACACACCTGAACCAATTAATTAGGACCTGAACACCATGGCTGCGTCCGAAACCGCATACTTCCATGCTATATAGTACGCTAAAATCAGTATGTGAGGCGAGTAGTATGTCCGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa947
Status:
F2 line generated
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:
A > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000109613 | Nonsense | 1662 | 1696 | 26 | 26 |
| ENSDART00000134349 | None | None | 605 | None | 9 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 44149787)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 43274957 |
| GRCz11 | 9 | 43076744 |
KASP Assay ID:
554-0852.1 (used for ordering genotyping assays)
KASP Sequence:
AATGTAAACTGATTTCCTCAGGTTGTAGGAACASTCCACACTTCCTCTCC[A/T]GAGTGGATGGGCAAAATGTACTGGTGGAAGAAGACCTCAGCTCACACTGT
Long Flanking Sequence:
TTATCTTTTTTTTTATTTAAAATGCTAATCTCATAACAATATTTATAAAACTGGATTAACTTAGTTTAAATCCAAATGTGTAAATAAATACTAGTAAATACTACAAAATTGTAAGTAAGTAAATATTACAAAATTGTAGGAAACATTTTTGGTGTGTTAAAACCATCCGATCACCATCCGACAACCGGATCCAGCAAAGATTAGTCCTTAAAATATCACTAAAATGCATAAATGAATTGAAAAATGAGGTGAGGAGCTGCAAAAAAGGTCCACTTTTTCTGAAAAAAGAGCCATGCCTTTCAATAGGCTGGCTACAGGCCTGAGTAAACAATAATGGAGGCTTAATGAGGCACATATTGACAACTCTATTTGAACTCTGAAAGCATTGTCAGCCACTTTTTTTGTGATGTTAATGCATTAATTTCTGCTTTATTTATTCAGTGCAGTTATAATGTAAACTGATTTCCTCAGGTTGTAGGAACAGTCCACACTTCCTCTCC[A/T]GAGTGGATGGGCAAAATGTACTGGTGGAAGAAGACCTCAGCTCACACTGTACTTATCCTCAAGTGCTCTGCCTGAAAGATTCTAAGGTTGCAGCATGTGACAAAAGCCCAGTGAGTCAAATGGTGTAAACTTAAATAAATGCAGTATATAATCTAAGAGCACTAGTTATAATCATTGTTTGATGTTGTTGCACTGTTTATTAAACACAATAAAATATTTAACTTTAACCTGTAGCTGTAATAAAAGAAGCTTTTTACATTTTTAAAAACCACATTAAAGTCAATAGTATTACCCCTTAAGAAATATATTGTTTTTCAATTGGCAAATTGTTATGCAACGAATGTCCTGATTACCCTAACTTGCCTAGGTAACCTAATTAGGCATTAAGCATTTAATTTGCACTTTGAGCTGAATACATCTTGGAAAATATCTAGTAAAATATTTTGTGCTTTTTTGTTGCGTTTTTTTTGGCTAAGATAAAATAAATCTGTTATTAGAAA
Associated Phenotype:
Not determined