ZMP
ccdc24
Ensembl ID:
ZFIN ID:
Description:
coiled-coil domain-containing protein 24 [Source:RefSeq peptide;Acc:NP_001014330]
Human Orthologue:
CCDC24
Human Description:
coiled-coil domain containing 24 [Source:HGNC Symbol;Acc:28688]
Mouse Orthologue:
Ccdc24
Mouse Description:
coiled-coil domain containing 24 Gene [Source:MGI Symbol;Acc:MGI:2685874]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32956 | Essential Splice Site, Missense | Mutation detected in F1 DNA | Not yet available |
sa45107 | Splice Site, Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa32956
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 > C
Consequence:
Essential Splice Site, Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000056656 | Essential Splice Site | 203 | 229 | None | 7 |
ENSDART00000114573 | Essential Splice Site | 203 | 397 | None | 8 |
ENSDART00000132221 | Missense | 204 | 210 | 6 | 6 |
ENSDART00000134024 | Essential Splice Site | 203 | 280 | None | 8 |
Genomic Location (Zv9):
Chromosome 2 (position 33152553)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 33451460 |
GRCz11 | 2 | 33434678 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTGACTGAAGAATCTGAAGCTTTGAGAAAAGATGTGCAGGCCTTGCAGG[T/C]AAGGGCTTATTTTGACGTTAATTACTGGTTTTGATTGCAACATCGATTTC
Long Flanking Sequence:
AGTTTTCATTTAAAAAATAGATTTTAAAAAAAAGATTCTTTAAAGAAATTTTCTCTAAAAAAGGTTGTTTTATGACATCCCTGTCAATACCAACCTGATCTTGCTAGAAAAAGTATTTTTTAAAAGTGTTTTACCTACAGTATTGGTGGAAAAGTGGCTAATTTGTATAAACTCATATGATTTCGTTCCTACAAAAAAAAAAAAAAAACTAAAAAAGAATGAGCAAATCTTGCAAAAATCTGCTAATGAATATGTAATTTTCATATGAATTAGCCACTAAATCAAAAAGTTACAATTTCCCATAAGAGAGTTTCGAGAAAACACCATTTTACTTCCACCTGGCCCCTTTTTAAAATATTTTCTGAGAGACTTACACTTTGTGACTGTTGATTCAAACTTATGCATATGCTGGCTTTCTAAAAGAGGGCTTTGTTTGCCTGACAGGTCAGTCCTGACTGAAGAATCTGAAGCTTTGAGAAAAGATGTGCAGGCCTTGCAGG[T/C]AAGGGCTTATTTTGACGTTAATTACTGGTTTTGATTGCAACATCGATTTCAGGATTACTTTAATAACATGCTATGATTCTGGATCTGAAGAGAGGAGGAATGTACAAAACAATGCCTCTGAGCGCTTGTTTTTCATATGTGAAGCACTTTTCTTTTGTGGTTTCTACAGTGTTTTAAGTCAGATCAGGTTTTAAATTCCTTTTTATATGGGTAAATAAGCATCGCAAAATAAAAAAAAAACCACGTTGTGTTTTCATAATGCAAGTTAGTCCATTGTTATGGTGCAGTATATTATGGCCTGTTTCCACTGAGTGGTACAGTATGGGCTGGTATGGGTCACCTTTATGAGGCTTGTGTTTCCACTGCCAAAAAGGTACCAATGGTGGACATGGCGTATGACAGAAAGTTTCAGTCAACGTTATTCTCACTTGAGAAAATGTCAAAGCTGAATGTTCATATATCATATGAGAAGCACTTCTCACCAAACAGAGGCTTTATAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45107
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:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000056656 | Nonsense | 228 | 229 | 6 | 7 |
ENSDART00000114573 | Splice Site | None | 397 | None | 8 |
ENSDART00000132221 | None | None | 209 | None | 6 |
ENSDART00000134024 | Splice Site | None | 280 | None | 8 |
Genomic Location (Zv9):
Chromosome 2 (position 33143582)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 33442489 |
GRCz11 | 2 | 33425707 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTACTCAGACAGAGCCTGTGTGCCCTGAACCCACATTAGCAGGTACATG[G/A]AGTTAATCCTGACAAATGACATTGGTTTCATGGCAGTTTTTTGGAGCAGC
Long Flanking Sequence:
TTATTTGATCAATTACAATTATTTAAAAGAAATATAAAAACTTTTTAGATTTTTTTTTCTTAAAACAAGCTAAATAATCTGCCAATCGGGTAAGGTAAATAATCTTAATTTCCACTTTGAAATGTAGATATTTGGACTAGAAGCAAGGCAAAAATTCCATGTAAGAACAACTTTTTTTTTGGTATAAATTGTAAAAATAATTAAATACAGGTCATTTCTCAATCAAAAGTGCTTTAAAGGGTCTGTGGCTCATTCTTTTATTTGTGCTGTTGAACTGTTTCATAAACACAATATGACGTGGAGATGTGTGATATGGCTGTATATCAGCACAGCTGTGATCACCTATAGTAAAAGCGTATATATTCTGTATATATTTAATGGTGTAAGTTGACGACTGTGGATTGATTTGTTTTGTTTCATTCACAGGAAAACCTTGAGGCTGAGCGAGTCAGTACTCAGACAGAGCCTGTGTGCCCTGAACCCACATTAGCAGGTACATG[G/A]AGTTAATCCTGACAAATGACATTGGTTTCATGGCAGTTTTTTGGAGCAGCCCTTTACATCTTTCTTCATAAACATTGCATCATAATGCCCATTTTATTTGAAATCTTTTCTCCAAATGTGATCTTTTTTGAATTGTGTATTACTACCATCTAGTGGTTCACCACTGAATTCTTATCCACTCCGTTCCACAGCTCAATAAAGAATGATCAAGGTTACTATCCTCAGTCTTTTCAGAGCAGAATACTTTTCAATTGAAGTAATAAAGCAGAATTTCTTTTATTTCTTGATTTTTTTTCAGGGTCATTATGAAAAGGTTTATCCTGGAGCAAAACTACCTTTAATTGATTCCTTGTCTTTCAGAGCTCAAAGAAGAACGGAGACTAATTCAGAGGGATCTGAATGTTCAGGGTTCAATGAGCTGCTCCTACAAATCAAACAATCGGAGTACCAGAAACCCACAAAAACACACAAGGTCAGTACACATTTCTAGAACAAGACTT
Associated Phenotype:
Not determined