ZMP
ccdc106
Ensembl ID:
ZFIN ID:
Description:
coiled-coil domain containing 106 [Source:RefSeq peptide;Acc:NP_001013323]
Human Orthologue:
CCDC106
Human Description:
coiled-coil domain containing 106 [Source:HGNC Symbol;Acc:30181]
Mouse Orthologue:
Ccdc106
Mouse Description:
coiled-coil domain containing 106 Gene [Source:MGI Symbol;Acc:MGI:2385900]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa43237 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa43236 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa43237
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 |
|---|---|---|---|---|---|
| ENSDART00000081465 | Nonsense | 323 | 357 | 6 | 6 |
| ENSDART00000104554 | Nonsense | 306 | 340 | 6 | 6 |
| ENSDART00000136653 | None | None | 232 | None | 6 |
Genomic Location (Zv9):
Chromosome 19 (position 10948373)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 10406912 |
| GRCz11 | 19 | 10325837 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGTCTGAGGTTGGAGAGTTTGATTCCTCCAAGGAGAAGCTTCTGGATTA[T/A]GCCAGACGCTGCTATAAAGCTCTTGATGAGGAAGCTCACGCAAAGGTGCA
Long Flanking Sequence:
GAAGAGGAGGAGGTGATTGAAGAGGAAGAGTATATAGCGGAGGAAGATTATGTGGAAGAGGAACAGCTCATTACAGATGACGATGGTAACATTTCAGAGGATAAAACCTCACGTAAAAGTTGTACAGGCAGGCTGAGTGGCCAAATGAGGGTGAAACGACGACGCGTCTTCCGTTTCGCACGAAGCATGGAAAGACAAAGGGGTGAGTATTCTTCATATGTATAAAATCAAACTCTATTTTTCCATACTTAAGTTCCTTTTGGAATAATTTCTGCCATTTCGTTTGCAGTGAAAGACCCTGCTGGTGTTCTGCTCCGCTACAATAAGATCCTCGTGACCTATCAGAAGCTGAAGAGCATGTCTAGAGCCTTTCAGGTCCACGGGGTTGACAGAAACACCGTCGCCTCCACTACTCCCATTGCTGAAATGCTCTTAGTTGCTCCTGAGAAGTTGTCTGAGGTTGGAGAGTTTGATTCCTCCAAGGAGAAGCTTCTGGATTA[T/A]GCCAGACGCTGCTATAAAGCTCTTGATGAGGAAGCTCACGCAAAGGTGCAGACCTTGAAGAAAACCAACCTCTTGCTGCCCATTTCCTACAGGTTCAGGCACTGAATTTCCAAAAATGTGTGTCAGTGGTGTTGAAGTTTAAACACTGAACTTTCATGGGCTCCTTTTTTCTACCTCAGTTATAGATTGACACATAAGGAGTGAAGTCCCAACTATGTGCCAGTTATTTATGCTAATTAGACTCCAAAGTTAAAAAGAAATGTAAGATAGTTAGTCAGCCACTGTATATGAGGGGTTACCTTTTCTTGTTTTGTGTATATGCTTGAGTTTCTTGTTGTAAACTTTGGACAACTCACTTTTTGTCCGGGTATCATGTAAGGTAACACTTCGGTTTTGTATACTGATCACACTTCATGCTAAAGGATGTTGATTTAAAATAAAGTTCATCACTTGCAATCATGCAAAAGAAAGTATAAAGGCCTTAATTATTTTTAAACTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43236
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 |
|---|---|---|---|---|---|
| ENSDART00000081465 | Nonsense | 353 | 357 | 6 | 6 |
| ENSDART00000104554 | Nonsense | 336 | 340 | 6 | 6 |
| ENSDART00000136653 | None | None | 232 | None | 6 |
Genomic Location (Zv9):
Chromosome 19 (position 10948283)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 10406822 |
| GRCz11 | 19 | 10325747 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAAAGGTGCAGACCTTGAAGAAAACCAACCTCTTGCTGCCCATTTCCTA[C/A]AGGTTCAGGCACTGAATTTCCAAAAATGTGTGTCAGTGGTGTTGAAGTTT
Long Flanking Sequence:
ATTTCAGAGGATAAAACCTCACGTAAAAGTTGTACAGGCAGGCTGAGTGGCCAAATGAGGGTGAAACGACGACGCGTCTTCCGTTTCGCACGAAGCATGGAAAGACAAAGGGGTGAGTATTCTTCATATGTATAAAATCAAACTCTATTTTTCCATACTTAAGTTCCTTTTGGAATAATTTCTGCCATTTCGTTTGCAGTGAAAGACCCTGCTGGTGTTCTGCTCCGCTACAATAAGATCCTCGTGACCTATCAGAAGCTGAAGAGCATGTCTAGAGCCTTTCAGGTCCACGGGGTTGACAGAAACACCGTCGCCTCCACTACTCCCATTGCTGAAATGCTCTTAGTTGCTCCTGAGAAGTTGTCTGAGGTTGGAGAGTTTGATTCCTCCAAGGAGAAGCTTCTGGATTATGCCAGACGCTGCTATAAAGCTCTTGATGAGGAAGCTCACGCAAAGGTGCAGACCTTGAAGAAAACCAACCTCTTGCTGCCCATTTCCTA[C/A]AGGTTCAGGCACTGAATTTCCAAAAATGTGTGTCAGTGGTGTTGAAGTTTAAACACTGAACTTTCATGGGCTCCTTTTTTCTACCTCAGTTATAGATTGACACATAAGGAGTGAAGTCCCAACTATGTGCCAGTTATTTATGCTAATTAGACTCCAAAGTTAAAAAGAAATGTAAGATAGTTAGTCAGCCACTGTATATGAGGGGTTACCTTTTCTTGTTTTGTGTATATGCTTGAGTTTCTTGTTGTAAACTTTGGACAACTCACTTTTTGTCCGGGTATCATGTAAGGTAACACTTCGGTTTTGTATACTGATCACACTTCATGCTAAAGGATGTTGATTTAAAATAAAGTTCATCACTTGCAATCATGCAAAAGAAAGTATAAAGGCCTTAATTATTTTTAAACTTTCTAAATTTATTTTAGAGCATTTCTAAACCAGCTTTTTGCTGTAAATTGATTCTTTAGCCAAAGCGTAAATAAATAATGTTTGACTGTAAT
Associated Phenotype:
Not determined