ZMP
zgc:114058
Ensembl ID:
ZFIN ID:
Description:
Coiled-coil domain-containing protein 22 [Source:UniProtKB/Swiss-Prot;Acc:Q4V909]
Human Orthologue:
CCDC22
Human Description:
coiled-coil domain containing 22 [Source:HGNC Symbol;Acc:28909]
Mouse Orthologue:
Ccdc22
Mouse Description:
coiled-coil domain containing 22 Gene [Source:MGI Symbol;Acc:MGI:1859608]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa41195 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa34393 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa41195
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 > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000099769 | Essential Splice Site | 416 | 639 | 9 | 16 |
Genomic Location (Zv9):
Chromosome 8 (position 24482297)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 23608115 |
| GRCz11 | 8 | 23629354 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGACCATTGACCTTCTTCCTGACGCTGAAAACAACCTGCTCAAATTACAG[G/A]TACACAAATCATTCCACGTTCACATCTGCCATCATAAGGAAAACAGTAAA
Long Flanking Sequence:
AATCAATCATAGTTATGGTAACAAAATGGTGTAATTTCTTATGCATAAATGCTTTTCAGGTTACAGGCTTCAAAAAGATATGCAAATGATGAATTACAATGCAAACTCAACATTGCATATATCCTGTGATGTGACTATTGCGAGTGATCACATTACAATATCGATGCTGAAACTTTATTTATATATATATATATATATATATATATATTATGCTGCCCTAATAGACATTATATTGGATGCATAGTAATTCACACTTTATATTGCATAATTAATGATGTAACAACTTTAACATGAGGAAATAATTTTTAAATTCTTCCATGAGTAATAAATAAATGCATTACTTTTTTAAAAACTTTGCTGACACTTTTTCTTGTTTTTAGGTGACAGATGAGCTGCAAACGAGAGAAGTGACTAACGCTGAGAGGGAGAATTCAGTCAAAATAAAAAGACAGACCATTGACCTTCTTCCTGACGCTGAAAACAACCTGCTCAAATTACAG[G/A]TACACAAATCATTCCACGTTCACATCTGCCATCATAAGGAAAACAGTAAAAGCTGGCATAACAGCACAGAGGAGCACAATGAAAGCACATATAATAGCCTGTGACTGATGGCATGTTTGTGTTTGTCTGTTCTGTGTGTGTGTTTGTGTTTTGGTAGAGTCTGGTGGAGTCCAGCTCTAAACGAGTGGTTCAGTTGGCCTCACAGTGGGAGAAACACAGAGTCCCGTTGATTGATGAGCACCGCAGGCTAAAAGAGCTGTGCAGCAACAGAGAGGTGCCTTGTGTTCTCCACCCATATAGAAAAAAACATGTCATATGTGCTTCTGTCTAGATATGGTTTTTCTGTCATTTTAGTTACTTGTTTATCAGCTAATAACTGGCTGGTTTGTTTATCTTACATATGTTGTTTGAGAATAACTAGTCATTTAAAAAAATTACATCATTTTTAATTTTATTTGTTTTTTCCTAATAATTTTAATCTAGTTTTAGGGCAAATCCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34393
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 |
|---|---|---|---|---|---|
| ENSDART00000099769 | Nonsense | 587 | 639 | 15 | 16 |
Genomic Location (Zv9):
Chromosome 8 (position 24487258)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 23613076 |
| GRCz11 | 8 | 23634315 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCTAACTTTTTTGTGCTCCCAGAACTGCACTCAGTTGATTCAGACCATC[G/T]AGGACACAGGAACCATCATGAGAGAAATCCGAGATCTGGAGGAACAGGTG
Long Flanking Sequence:
TACAGATTACAAAACTAAAATGCTTTTGTTTTCAAGTGTAATGGGTTCAATTAAAAATAGAGATTTTAAGCTTTATGTGGATATACTTATGTCTGTGAAGCAATTATTCACTGAGATTCCAGTTGGTTTGTTGACCACATAAATTGTCATAAAAGCACGCGTCTGGTCTCAGCTTCTCCCTTAGAGAAACGTCAGTCTATAGCCATCATCGATTGGCCTCAGTACTAGTAGGCGGGCTTCAGTAACTAAATTGAAAGTTACACTTTTCCTCATTTAAAACTGTATTAGCGACATGTCTTGTGTATTATATAGTCTTTGGCTCTAGTCATAAGCAGTACTTTAATCCATCTGTTTAACATCTAAAACATATTAAACACAAAAGAGTTAAGAGCCTTTAGCGACTACATGCTTTTAGCATTTTTTCCTGCAAGAGATTTTTCATTTTCATCATTCTAACTTTTTTGTGCTCCCAGAACTGCACTCAGTTGATTCAGACCATC[G/T]AGGACACAGGAACCATCATGAGAGAAATCCGAGATCTGGAGGAACAGGTGTGAGACAAACCAGTATTTAGAGGCACTTTCATTTGTCAAGACTTATACAAACATGCCTCCATGTCACTTTTCGACTGTGAGAAAAGTAGGTCAGATGCTCAGACTGTTCTGACTTGGTGTGATAAGTCTTTCGTAACTCATTGAACTTGCAGTTCTAACAAGCAAAACTTCCTATAGACCCACATTGACAGAATGATTAAATGAGCCCAGACTATAGAGCTCAACTAACTGGTTCCGGAAGTTATATCACCATTCATTTATATATTGGGAAATTGATTTTAAACATTCACTGATAAACCTTTAAAACAAACCTTGTGAACTCTTAGGGTGTTAATCGATTGCATATGCTTTTTTTCTTTTATTTAAACTTATGAAATGATTGTTTAATAGTAGACTTCAGGCAAAAAAACTATTTGGCACATGATTCCATGCCGAAAATAACAATCAGAG
Associated Phenotype:
Not determined