ZMP
ccdc65
Ensembl ID:
ZFIN ID:
Description:
Coiled-coil domain-containing protein 65 [Source:UniProtKB/Swiss-Prot;Acc:Q6DHI2]
Human Orthologue:
CCDC65
Human Description:
coiled-coil domain containing 65 [Source:HGNC Symbol;Acc:29937]
Mouse Orthologue:
Ccdc65
Mouse Description:
coiled-coil domain containing 65 Gene [Source:MGI Symbol;Acc:MGI:2146001]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa20626 | Nonsense | Available for shipment | Available now |
| sa6066 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa20626
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 |
|---|---|---|---|---|---|
| ENSDART00000043946 | Nonsense | 27 | 492 | 1 | 8 |
The following transcripts of ENSDARG00000032005 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 6 (position 7338822)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 6 | 7264838 |
| GRCz11 | 6 | 7422007 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGGAAAACTGGCCGGGTTGACGGAGGAGGAGAGACTCCTGTACATGCAG[C/T]AAAAGGCTCAAGCGGAGGAGGAAATCGCCAAGAGAAAAGAGGACATGCTC
Long Flanking Sequence:
CTTGTGAGTTTCTTCTTTTGCTCCGGTTTACCCCACAGTCCAAAGACAAGTGCTGTCGGTGAACTGAATAAACTAAATTGGCCATTGTGTATGTGTGTGAGATTGAGTGAGTATGGGTGTTTCCCAGCACTGGGTTGCAGCTGAAAGGGCATTCGCTGTGTAAAACATACGCTAAATAACTTGGCGCTTCATTCCGCTGTGGTGACCCCTGATCAATAAAAGGACTAACCCCAAGGAAAATGAATGAATGAATATTGGAAATTGGCTTCAATATCCCAGGCTCTGGAATCAAACATCTTCTCTGGATGATAACGTAATCATAATAATCCTGTTGATGGCTCGGTATATGGTTCTGATTTTGTGTAGTTACACAATGAATTTTCTCTTCTCAGGAATTCTGAAATCTCCGAAATTCTGCAAACATGCCTAAAAAAGCAGGGAAGAAGGCCGGTGGAAAACTGGCCGGGTTGACGGAGGAGGAGAGACTCCTGTACATGCAG[C/T]AAAAGGCTCAAGCGGAGGAGGAAATCGCCAAGAGAAAAGAGGACATGCTCACACACTTCCTCAAGGTGTGTGATAATCAGTGTGTTTGAGGAGCATGGGTTTTTGTAAACCAACATTGAGTCAAATCTAGACAAACCCAATGTTGTGTAGTTTTCAATGAAATGTAAATGACACTTTTAAACCAACAGTTGGGTTTTGAAATCAGTTTAAATGTTTTATAGTTTTGATGCTTGAAAACCCGATTACGTCCCACATTTTTGTTGTACTGCATAAACATCAGAAATGTTTAGTTTTTTAAATATGTACTTAGCACTAATTAACACAAGCTGTTTAAGGCTTATAAGGCTTAAGGGATTTCCACTCTTGTTTTTATAGGATAAACTGCAGAAAGAAGAGAAGAACACTGTACTGAACCTCCACAAGCTGCGTCAGCAATGGCGAGCTGTTTTGACGCAGACAAAGATAGCAGAGCTGCGCAATGACATGTCAGTCCTCTCGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6066
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 |
|---|---|---|---|---|---|
| ENSDART00000043946 | Nonsense | 141 | 492 | 3 | 8 |
The following transcripts of ENSDARG00000032005 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 6 (position 7339850)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 6 | 7265866 |
| GRCz11 | 6 | 7423035 |
KASP Assay ID:
554-3855.1 (used for ordering genotyping assays)
KASP Sequence:
ATCTGCAMAACGTGGACTGTCTGTTAGAGATTCATAAGAGTCGACTGGCA[C/T]AACTAGAGTTCAACTTCAAGAGCAGTCTRGWGGAACTTAGCTCAGAGTAT
Long Flanking Sequence:
AGACAACATCATTAGGGTGACCACTTTATTTGCAAACGAAATGCATTTAATATAAACCACAGGCGTCAAAGCCAGATCCTTGAGGGCCACAGCTGAACTAACACCGAACTAAGTCCTTCAGGCTTGTTTGCAACCTACAGAAAAGTGTTGAAGCAGAGTTGGAACTTAACTGTGCAGAGCTGCGGCCCTCCAGGAACTGGCTTTGACACCTATGATATAAACTATACAAGTCTGATATATAATATCATATAATATAATATAATATAATATAATATAATATATGATTTTTAGACATATATAATATAAAAGTATGTCTAAAAACATTAAACGTGTGGTTGTGTGTGTGCGTGTGTGTGTGGGTGCGTGTGTTTGTGTGTGTGTGTGTTTTCCAGAGTTTGCAGGTTGATTTGTCAGAGAGGGAGCTTCAGTCGGAGCTGAAGCGCAGTTCACATCTGCACAACGTGGACTGTCTGTTAGAGATTCATAAGAGTCGACTGGCA[C/T]AACTAGAGTTCAACTTCAAGAGCAGTCTAGTGGAACTTAGCTCAGAGTATAATACTGAGAGGTATACACACATGAACTGTCTCATATTCCCAAAATACTTACAAATGCATTCATTCATTCGCCTTAGTCCCTTATTTATCATGGATTGCCACAGGGTGATGAACCGCCCACTATTCCGTCATATGTTTTACGCAGCGGATGCCCTTTCAGCCGTGAGCCAGTACTTTGAAATACCCATACATTGTCACATTCACACTCACTCTCATACACTACAGGCCAGTTTAGGTTATCCAGTTCACTTATTACGCATGTCTTTGGACTGTGGAGGAAACCAGAGCACCTGGGGGAACCAAAGACATGCGCTATAGGTGAGTTGGGTAAGCAAAAATTGGCCGTAGTGTGTGAGTGTGTGTGTGAATGGGAGAGTGTATGGGTGTTTCGCAGTACTGGGTTGCGGCTGGAAGGGCATCCGCTGCATAAAACATATGCTGGAGTAGTTG
Associated Phenotype:
Not determined