ZMP
ccdc146
Ensembl ID:
ZFIN ID:
Description:
coiled-coil domain-containing protein 146 [Source:RefSeq peptide;Acc:NP_001076522]
Human Orthologue:
CCDC146
Human Description:
coiled-coil domain containing 146 [Source:HGNC Symbol;Acc:29296]
Mouse Orthologue:
Ccdc146
Mouse Description:
coiled-coil domain containing 146 Gene [Source:MGI Symbol;Acc:MGI:1922422]
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa33456 | Splice Site, Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa14673 | Essential Splice Site | Available for shipment | Available now |
| sa15556 | Essential Splice Site | Available for shipment | Available now |
| sa11874 | Nonsense | Available for shipment | Available now |
| sa20266 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa33456
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:
Splice Site, Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000017947 | Splice Site, Nonsense | 153 | 860 | 4 | 16 |
| ENSDART00000121843 | Splice Site, Nonsense | 153 | 953 | 3 | 17 |
| ENSDART00000135451 | Splice Site, Nonsense | 153 | 410 | 4 | 9 |
Genomic Location (Zv9):
Chromosome 4 (position 19122063)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 4 | 20465398 |
| GRCz11 | 4 | 20186373 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCGAATGCAAGGATGTTTTTTTTTTACAGAATTTCATTTCTGCTTTTTAG[T/A]CTTAAAGAGGAAAAGCTCTATCTTGAGAAAGAATACCAGGATCAACCTAA
Long Flanking Sequence:
GAACCTCTGTACTAGAGAGTACAGTATACAATATGCAATACGATATATGTATTTTATGCATGTCAGTTAGTCAAGTATTCCTACTGCAGGCATATTACTGCCAGATGTCTTTTCTGCACATGTGGATATTTTGTCCTGAGTGAATCCTTCATCCCTATCCAAACCAGCATGGATACACATTGCACAGCATGCTTTCGCTCACTGTAATAATCTACTACTTTGATGGGATGGTCCAGCTTTCAATGATAGCAGTATTAGCATTCAGCTAGAATATTTATACATGTGGTTTTCACACAGCTTGTTATTGCACAGCTTTGTCATCTAAAATGTTTAATAGCAGGCACAACATTTATAAATGTGAAATGTCCTGTGTGCTTAAACGCTTCTCTAATTGTATAATTTGCATTTATTTGTTCCTTTTTATTTGAATTGGTTTACATCCTGATTTCTGCGAATGCAAGGATGTTTTTTTTTTACAGAATTTCATTTCTGCTTTTTAG[T/A]CTTAAAGAGGAAAAGCTCTATCTTGAGAAAGAATACCAGGATCAACCTAAACAGGCTGTAAGTATAGCTAGGGCATGTGACGTCTCCAGATAAATACATCATTGGGTTTTCCGATACACTGTAAAAATGCTTGGAACCACACAATTTCTTCATGGTCTCTGAACACATATTGATTGTTAACTTAAATGTTTTTAAAAAAAAATTTAAAAGTGGGTTGACCACAAAAAAATTAAGTTGTCACCCGACCCCCCTCCCCCAAATACCCTTTTTCTTAATTGTGTTGTGTTGATTCCACTCATTTTAAATAAGTAGCTTAAATAAAGCAAGCAGTGTGTGTGTGTGCATTAAGATGCATTATACTTAGGGCCAGACAGAATCTGTGGACATTTTTAGCTATTTCTGCAGAGAATTTTTGTTAAAAAAAAAATCTGGATTTATGTGGAATGATTTTAGGAGGATCATAACTAAAAAACTTAATTACAAAAAAACAAACATGACAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14673
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000017947 | Essential Splice Site | 474 | 860 | 10 | 16 |
| ENSDART00000121843 | Essential Splice Site | 512 | 953 | 10 | 17 |
| ENSDART00000135451 | None | None | 410 | None | 9 |
Genomic Location (Zv9):
Chromosome 4 (position 19126398)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 4 | 20469733 |
| GRCz11 | 4 | 20190708 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGACTGGTTATACAGGAACACATTAAWCAGACTAAAGAGACACAGACAAG[G/A]TACTACCAGATTGACTGAAACAGAGCTGATGCTAAAGCAARATAKAATTT
Long Flanking Sequence:
TGAAGGTCCAGCTGGTTCAAGAGTATGTTGAGAAGGAGCAGGCTTTGATTAGAGAGTCTTATCGCCGCAGAGATGAGCTTCATCACCTTCATCATCTCATACTTATCAAAACAGACGAAAAAGAGCAGAAGAGCCGTGAGCTACTGAAAGCACAGGTTATTTACATTACATTACATTTGCCTCGCATTGCATTTACCTCTCAGTCCGTATTTATTCACCATCATATTGTTCCAAAAAGTGGAATTTTCCTGCTCCTATTGGAAACATGGAATGACTAACTTTCAAACGTACAAAAATTAGTACTGTCAAATGTTTTTCATGACGGTTTGGAACAACATGAGGGTAAATAAATCATGATTAATTGATAATTTTTGTCTTTATGCCTACTGATTGATATGAATGTCATTGCAGCTCAAATACAAGCAATCTAAGCAAGAACTGCAAGGAAAAGGACTGGTTATACAGGAACACATTAAACAGACTAAAGAGACACAGACAAG[G/A]TACTACCAGATTGACTGAAACAGAGCTGATGCTAAAGCAAGATATAATTTTAAAATGCTTTTGTTTTTCTTTTATTTGCCTGATTTAAAAATGAACCTAGTTTATTAACCTGCTGTATAGTCTGATTAGTAAATGGGCTCTTTAATGTTACCCTAACCAGGCTGGGCGTGTTTGCTAAGCTGTATGAAGTCACCAAGTCTAAGCGGAACAAGTACCTGAGCTTAATTCAAATCTCAGACCAAAACCTGGCATTGGTGCAGGAGAAGCTGGCTAAACTGGAAGAAAACCTAAAGACACTGCAGTCCACTGCTATCAGCAAAGACAAGTTCCTTACCTTTCACATGCATATTCTTATTCTTTTAACAATCTGACTACCTACCACAAAGTAACACTTACCTTTACTGTGAAGTGCTATGAGTGTGCATATTTGCTCGAAGTTTGGCATTATTTGAACTGAGATATGGTGGTAGGGTGGGACATAATGTAGTTCCTGTCTCTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15556
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:
G > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000017947 | Essential Splice Site | 549 | 860 | 11 | 16 |
| ENSDART00000121843 | Essential Splice Site | 642 | 953 | 12 | 17 |
| ENSDART00000135451 | None | None | 410 | None | 9 |
Genomic Location (Zv9):
Chromosome 4 (position 19127707)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 4 | 20471042 |
| GRCz11 | 4 | 20192017 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTACATATCTGCAAGCGCTATGAGGCCGAACTGCAAAAGCGGAATCAAGA[G/T]TGAGACATAGAGTCTGGGGGATACAAATCTGGCAGGTGAATTCTCACAGT
Long Flanking Sequence:
GGACATTAAAGATTGCTCAACAATGAGATTTATTTTCGCTTGTATGGTTGAGTTTCTGTTTGTGTTCAAACTAAATGTTGTGTGATCCAAACTAAATCCAATGTGAGGCCACTGTAAAAAAATATTGACAAAAAGTCATGACTACAAATGTTTAAATTAAATATAAAAAAAATATTTTAAGTCTGTTTGATTAATGTAAGTTGAGATGGTAATTTTAATCAACTAAAAAAATTAAGGTAGCAAGAATTTTCTAAGGGTCCTTTTATTTCCTGCAGGTTACTGCAGAGATCTCGTCTACAACACTCTCACAGCTACAAGCTAAGAGACGATCTGAAGAAGGAGGTCTCACAGACATTACAGGCTTTGCAGGAGATGCAACAAAATCGAGAGGAGCAAAAACTAAAACTCAGGAAGCTCACGGACACCGTGAACATGCTAGAGCAAAAAAAGCTACATATCTGCAAGCGCTATGAGGCCGAACTGCAAAAGCGGAATCAAGA[G/T]TGAGACATAGAGTCTGGGGGATACAAATCTGGCAGGTGAATTCTCACAGTCTGTGCTGATATTTCTATCTGTGTTTTTGTTGTCAGGTCTGTGCAGCTTGCAGAAAGAGAGAAGGAATGGCGTATTTTCAATGAGAAGCTTGGTGTACTGGTGAAAATGACTGAAAACAGCAACTTGGAGATGTATGACATGGAAGATGAAATCAGAAACTTGAAAATGGAACAGAAAGAAGAAGAAAGACAGAATGATCTGCACAAAAAGCAGTTGTCAAACAAACTAGCTCTGGAGGAAGAGCGTGTCTTATTACAGATACAGGTACCTGGATCACAATTTTGAAACCACTGTGAAACATTTATCTGTTAAAAAAATTGCATCAGATGCACACAAATATGTGAATCAAGTGCCAACAATACAATCTCTAACAGAGCAAACAAACACAGTGGAATGCAAGTAAAGGTTAGATTTAATGCCTTCTAAAGTGCCACACATACCCACACACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11874
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 |
|---|---|---|---|---|---|
| ENSDART00000017947 | Nonsense | 595 | 860 | 12 | 16 |
| ENSDART00000121843 | Nonsense | 688 | 953 | 13 | 17 |
| ENSDART00000135451 | None | None | 410 | None | 9 |
Genomic Location (Zv9):
Chromosome 4 (position 19127930)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 4 | 20471265 |
| GRCz11 | 4 | 20192240 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACTTGGAGATGTATGACATGGAAGATGAAATCAGAAACTTGAAAATGGAA[C/T]AGAAAGAAGAAGAAAGACAGAATGATCTGCACAAAAAGCAGTTGTCAAAC
Long Flanking Sequence:
TAAAAAAATTAAGGTAGCAAGAATTTTCTAAGGGTCCTTTTATTTCCTGCAGGTTACTGCAGAGATCTCGTCTACAACACTCTCACAGCTACAAGCTAAGAGACGATCTGAAGAAGGAGGTCTCACAGACATTACAGGCTTTGCAGGAGATGCAACAAAATCGAGAGGAGCAAAAACTAAAACTCAGGAAGCTCACGGACACCGTGAACATGCTAGAGCAAAAAAAGCTACATATCTGCAAGCGCTATGAGGCCGAACTGCAAAAGCGGAATCAAGAGTGAGACATAGAGTCTGGGGGATACAAATCTGGCAGGTGAATTCTCACAGTCTGTGCTGATATTTCTATCTGTGTTTTTGTTGTCAGGTCTGTGCAGCTTGCAGAAAGAGAGAAGGAATGGCGTATTTTCAATGAGAAGCTTGGTGTACTGGTGAAAATGACTGAAAACAGCAACTTGGAGATGTATGACATGGAAGATGAAATCAGAAACTTGAAAATGGAA[C/T]AGAAAGAAGAAGAAAGACAGAATGATCTGCACAAAAAGCAGTTGTCAAACAAACTAGCTCTGGAGGAAGAGCGTGTCTTATTACAGATACAGGTACCTGGATCACAATTTTGAAACCACTGTGAAACATTTATCTGTTAAAAAAATTGCATCAGATGCACACAAATATGTGAATCAAGTGCCAACAATACAATCTCTAACAGAGCAAACAAACACAGTGGAATGCAAGTAAAGGTTAGATTTAATGCCTTCTAAAGTGCCACACATACCCACACACAGAGAAGTGTTGTTTTTACCATTTATAGTCCCTTCTGTAAATGAAATAAACCATCTCAGTGAAAATCCGCCTGATAGGTTTATAGACCTCTGTGTTTAAACAACAGAGTCTCTGCATATCAACATTTACTGCATTAGAACAGATCAAATAAACAGTACTAAGACTTTACAATAAAAAATGCCTCGTCCTTAGATACCAGGCAATGACAAACGGTACTGTAGTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20266
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000017947 | Essential Splice Site | 625 | 860 | 12 | 16 |
| ENSDART00000121843 | Essential Splice Site | 718 | 953 | 13 | 17 |
| ENSDART00000135451 | None | None | 410 | None | 9 |
Genomic Location (Zv9):
Chromosome 4 (position 19128023)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 4 | 20471358 |
| GRCz11 | 4 | 20192333 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTCAAACAAACTAGCTCTGGAGGAAGAGCGTGTCTTATTACAGATACAG[G/A]TACCTGGATCACAATTTTGAAACCACTGTGAAACATTTATCTGTTAAAAA
Long Flanking Sequence:
AGCTAAGAGACGATCTGAAGAAGGAGGTCTCACAGACATTACAGGCTTTGCAGGAGATGCAACAAAATCGAGAGGAGCAAAAACTAAAACTCAGGAAGCTCACGGACACCGTGAACATGCTAGAGCAAAAAAAGCTACATATCTGCAAGCGCTATGAGGCCGAACTGCAAAAGCGGAATCAAGAGTGAGACATAGAGTCTGGGGGATACAAATCTGGCAGGTGAATTCTCACAGTCTGTGCTGATATTTCTATCTGTGTTTTTGTTGTCAGGTCTGTGCAGCTTGCAGAAAGAGAGAAGGAATGGCGTATTTTCAATGAGAAGCTTGGTGTACTGGTGAAAATGACTGAAAACAGCAACTTGGAGATGTATGACATGGAAGATGAAATCAGAAACTTGAAAATGGAACAGAAAGAAGAAGAAAGACAGAATGATCTGCACAAAAAGCAGTTGTCAAACAAACTAGCTCTGGAGGAAGAGCGTGTCTTATTACAGATACAG[G/A]TACCTGGATCACAATTTTGAAACCACTGTGAAACATTTATCTGTTAAAAAAATTGCATCAGATGCACACAAATATGTGAATCAAGTGCCAACAATACAATCTCTAACAGAGCAAACAAACACAGTGGAATGCAAGTAAAGGTTAGATTTAATGCCTTCTAAAGTGCCACACATACCCACACACAGAGAAGTGTTGTTTTTACCATTTATAGTCCCTTCTGTAAATGAAATAAACCATCTCAGTGAAAATCCGCCTGATAGGTTTATAGACCTCTGTGTTTAAACAACAGAGTCTCTGCATATCAACATTTACTGCATTAGAACAGATCAAATAAACAGTACTAAGACTTTACAATAAAAAATGCCTCGTCCTTAGATACCAGGCAATGACAAACGGTACTGTAGTTGAAGCACATCTTTTCACATCACGTACATTTGTCAAAAATACAACAAAGTTGATACTCTGACATGAGCATCAGTTAGCATATTATAATCATTTCT
Associated Phenotype:
Not determined