ZMP
cdca8
Ensembl ID:
ZFIN ID:
Description:
Borealin [Source:UniProtKB/Swiss-Prot;Acc:Q5XLR4]
Human Orthologue:
CDCA8
Human Description:
cell division cycle associated 8 [Source:HGNC Symbol;Acc:14629]
Mouse Orthologue:
Cdca8
Mouse Description:
cell division cycle associated 8 Gene [Source:MGI Symbol;Acc:MGI:1196274]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa43351 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa43350 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa43351
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 |
|---|---|---|---|---|---|
| ENSDART00000063337 | Essential Splice Site | 193 | 276 | 8 | 11 |
Genomic Location (Zv9):
Chromosome 19 (position 49499384)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 48149405 |
| GRCz11 | 19 | 47778466 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTTCAATCATCGGTGCCACACCGCTCATCACGCCGCGCTTTGACCCCAG[G/A]TGAATTCACAACACTGCATTTTCATGACACTGTTGATTAAAACTGCACAC
Long Flanking Sequence:
AATTATGAGAAACAAGATGATGAGAAAAGGATAAACGTTGGTCCATGATGAGATGGACTGGAAAGCAGAAATCCGAATCCTTCAGTATTTATTTTTTTGGTTTGCTCAGCCAAGTCTATTTTGATAGGTCTATGTTGGAAATTAAACTCCTGTTTCAGTGATTGTTGTTTGTCATGGGAAGCTTTATTTGAAACTACATGTTTTACTGTTTCTGTGGTGCAGAAGAAGGCCTCAAAGAAAGCTCCTTCAACGTCCAAGAAGCCCAGAGCTCTGTCCATCAGCAAACAGGGCGGCACCATCCAAAGGTGAAGAGAATCTGCAGTCTCCCCTGTTTAATAGGATTAACATTGTTTCTGTCCTGATGGTGTTCAGAAGTGTCAGTTCAGGTCTGCTTTTGTCCACAGGACTACAAGGAAGCCTCTGATCACTCCTGCTAGAAGTTTCCTGGACTCTTCAATCATCGGTGCCACACCGCTCATCACGCCGCGCTTTGACCCCAG[G/A]TGAATTCACAACACTGCATTTTCATGACACTGTTGATTAAAACTGCACACTGATACAAGTAAATTGTTGGATTAGAATTGAGAATATTAAAAAAACTAATGGAATTACAAGGTCATATTTCAGCGTGGCACTACACTAATACCAATCAAAGTTCCTACAAGGAGTGAGTTGCCAAGGCACTCGTCACTTTTGAGGAAGTCCAAGTAATCTTATTTTATCTTGATAACAATAACTCAACAATATTGAACTTTGATCGCATGTTTTTGTGCTTATGCCTTCTTTTTTCGGCTTGTAATAGAAACGTATTAGAGAAACCACCAGTAGACATGCAACTCTTAGTGAACGATTCAGTGAATCTCTCTTTAAGGAGAACTGTTTGATTAAAAATAGAGCTAGTCAAATGATTAATCCTGAAACTGATTAATTCAGGAAGGAAAAGCCTCTGACTACATTTACATGGACGTCAAAAATTAGATTTTAATGCGATTAAGACAATACTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43350
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 |
|---|---|---|---|---|---|
| ENSDART00000063337 | Essential Splice Site | 236 | 276 | 9 | 11 |
Genomic Location (Zv9):
Chromosome 19 (position 49496819)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 48151970 |
| GRCz11 | 19 | 47775901 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGCCGGTGGAGAAGACATCGTCATCAGTGTCCCGATCGGAAACGGAGAG[G/A]TAGATGGTGATCCTGATGCTCATTAAGCACAGCTCAGTGTTTGTGTGTTC
Long Flanking Sequence:
TCATCAGTGATCGAGAACTTGTTTACTGTTGTAAGATCCGTGTACCACTATTGGTGCGCAGGCTTCCTTCTAGTGGTATGCGGAGAAATTAAATATGTAATGTACATGCTACACATTTAAAAATGTATAAAAAATGATCTATATAATATGCCATATATGAAAAATAGCCTATATTTCTGAGGTAATCAGCCCCGTTTTTTTTTAACTGAGGTGTAGCTGCTTTACTGGGCCTACTGCGCTATTGTATTTCAATACTGCTCATTATGGTGGTACTTGGAGAGACTATTTATATTTCTGAGGTGGTACTTGATGGAAATAAGTTTGAGAACAACTGCTATAGGTCTTGACATTGTGTGTTTGTGTGTGTCAGATTGCCCAAGACTCCAGCATTGAGATCAGCTCTTCACAGAGAGAAGGTTTACAGCATGTCAGTGAATGGATCTCCTCTGTCTGCCGGTGGAGAAGACATCGTCATCAGTGTCCCGATCGGAAACGGAGAG[G/A]TAGATGGTGATCCTGATGCTCATTAAGCACAGCTCAGTGTTTGTGTGTTCGAGTGTGTGACGTGTTTTCTTTGTTATTTTCAGTGTATTCAGCTGCTGGCCAGTGAGATGGACTCTGTGGATCTGAGTCAGCTGGACGAGAAAGCTCTTCGCAGTATCAGAAACCTGCAGGTATGAGTTTCTGTCTTCATTCTCAGAGACCGTTCCCTTACAAATATTCAATATTGTCATTTATTCACCGTTCAGTTGAACCTGACCTGTGACTGAGTAGTTCTTCTGTTGAACACAAAAAGAGGATATTTATTATTTTATATTTGCACAATTTAAATTGCGCATGTCCATTGCCGTATATTGCACAAATTCATCTTGAATTGTACATACTCACTGGCCACTTTATTGGGTACACCTGTCAAACGTGGCATGGTTGTTGCTGCCAGACGGGCTGCTCTGAGTATTTCAGAAACTGCTGATCTACTGGGATTTTCACGCACAACCATCTCT
Associated Phenotype:
Not determined