ZMP
zgc:171667
Ensembl ID:
ZFIN ID:
Description:
centromere protein O [Source:RefSeq peptide;Acc:NP_001099172]
Human Orthologue:
CENPO
Human Description:
centromere protein O [Source:HGNC Symbol;Acc:28152]
Mouse Orthologue:
Cenpo
Mouse Description:
centromere protein O Gene [Source:MGI Symbol;Acc:MGI:1923800]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa36302 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa36301 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa36302
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 |
---|---|---|---|---|---|
ENSDART00000109249 | Nonsense | 84 | 284 | 3 | 6 |
Genomic Location (Zv9):
Chromosome 17 (position 6297180)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 6376116 |
GRCz11 | 17 | 6533346 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGATGAAGAGGATGAGGATGATGAAACTGGAGGCTTCGCAGCTCTACAA[C/T]AGTCTTTGTTAACAGCTTGGAAAATGCAGCTGAAAGATCTTCAGCACGCA
Long Flanking Sequence:
CGCTGCGTAAAACATATGCTGGAATAGTTGGGAGTTTCATTCCGCTGTGGTGACCTCTGAAATAAAGACTAAGCCGAAGGAAAATAAATGAAGTTACTGTGTATTAATGATAATGTGGAAAGCAAAATAATCTTGTTTTTCCTTTTGACATAATATTAATTTGCTTACCCTTTTGGCAGATTATTTTGCTTGTTTTAAGGAAAAACTCACTTAATATTGGCATATTATTTCTCAAAACAAGACAATATGTTTTGCTTGTCTATGAAATTCTTTGTGATTTGAGAATTTTTAGATAGTTGAACTCGAAACAAGACAAAAAATCTAAGTAAGAAAAGCATTTTTTGCAGTGTAATATTGGTGTAATTATTGTTTTGGTGCATGTTTTAATACCTGTTGTCAATGTACTGCAGACCCTGAAAGATAAAATCAGCAAAAATCTTCCTTTTGAATATGATGAAGAGGATGAGGATGATGAAACTGGAGGCTTCGCAGCTCTACAA[C/T]AGTCTTTGTTAACAGCTTGGAAAATGCAGCTGAAAGATCTTCAGCACGCACATCATTTAATAGGTAAACACATACAAATATGCAAAGTTTATTTTTAAACTAATTTCGAGAGGATCACATGCTTATGATTGCTTGCAGCTGGTCCTGCATTATTCAATTTATGATTCACCAATCAGACCATTTCTAAGCCACTATAAATACCCTAAAGGCCCGTGCACACCGAGACGTTTTTGCTCGCGTTTTCCATCGACGTTTAACGCCTCATAACTATATAAAGGGCGTCAATGTGATCGTGCACACCAACGCGCAAAACGGCAGGCGCAAAAGCGTCATTTAAAAAAAAAAACACCTCATGCTCGTTTTTTTGTTTTGACGCGCTGCATCAAAACCTTCTCCACCAATCAGATCGGCACCTTTGTTCACGTGCACGGAGCTGCTGAAGATACCGAAAACAGCACTTGGAGGCGCTCAAGCGCAAAACTGTCAATGCGAGCGCACAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36301
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 |
---|---|---|---|---|---|
ENSDART00000109249 | Essential Splice Site | 248 | 284 | 5 | 6 |
Genomic Location (Zv9):
Chromosome 17 (position 6292431)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 6371367 |
GRCz11 | 17 | 6528597 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAAAGATCTCACACAGAGTCTCCCAACACACGTCAGCATTGAGAGTGAAG[G/A]TACAATCCAATACCAAGAGAAACTGAACTACAAGTGTGAACAAACCATGT
Long Flanking Sequence:
TACTGCAGGGCTGCCCAAACTCAGTTTTGGAGGGCCGGAGTCCTGCATATTTTAGTTCCAACTCCAATTAAACACAACAAAAGCAGCTAATCAAGCTCTTTCTAGGCATACTAGAAAGCTCCAGGCAGGTGTGCTGGAGGAAGTTGAAGCTAAACTATGCAGGACACCGGCCCTCCAGGACTACGTTTGGACACCCCTGTCTTACTTAAACCAAACCCAAAGAAACAGAATTATCAACTAGTCTCCTAAGTTGTTTTTTTAGCTGTATATTTTGTGACATGGTAAATATCTTTAATATTTATCAACATTATGTCAAAATGCATTGTCTTTTCCGCAGGATCTTGTTGGTTCGGTGGAGGTGATGGAGAGCAATGAGCTGTGCAATATTCTGGTGCTCATGTGTTCAGCACAAAGCGAGCCCCCCAGAGCTGTTTTATGCACGCTGGAGTATAAAGATCTCACACAGAGTCTCCCAACACACGTCAGCATTGAGAGTGAAG[G/A]TACAATCCAATACCAAGAGAAACTGAACTACAAGTGTGAACAAACCATGTTGCTGTTATTGACATGAAATTTATTTTAGAGTAAATGTAAGGATCTTTACTTGATAAAGGTGATGCACAGTTTAATCTAAAGCATGTATTTTATTATGAGACGGAAAAGGAAATGATGGCGTTCATTTTGTATCATATGCTTGCTTTTTTTGTAGATAAAACACTTTCTGGATCTGCACAGTGGAAGACAAACCAGGCTTTACTCCTGGAGTCTCCGGCTCACACGGCTCTCCTGACCATGAAGAGGATGGGAAGCATCGTCTAAGAAACAGGAGGAAATTAATAACTTTATTGAACATGTAAAGCATTTCCTGGAAACTCTTTCAGTGGGCTTAAACAGTTAAACGCTTTTATATTCAGAGGCAGATATACTAAAATGAAGATTTTATATAAAGACCCAAAAATGTAAAAAAAAAATACTTCATTTACTCACCCTTTGCTGCTACTTTT
Associated Phenotype:
Not determined