ZMP
cep68
Ensembl ID:
ZFIN ID:
Description:
centrosomal protein 68 [Source:RefSeq peptide;Acc:NP_001007172]
Human Orthologue:
CEP68
Human Description:
centrosomal protein 68kDa [Source:HGNC Symbol;Acc:29076]
Mouse Orthologue:
Cep68
Mouse Description:
centrosomal protein 68 Gene [Source:MGI Symbol;Acc:MGI:2667663]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22289 | Nonsense | Available for shipment | Available now |
sa35481 | Nonsense | Available for shipment | Available now |
sa44786 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa22289
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000057588 | Nonsense | 164 | 650 | 3 | 6 |
ENSDART00000125949 | Nonsense | 164 | 685 | 2 | 6 |
ENSDART00000147514 | None | None | 126 | None | 4 |
Genomic Location (Zv9):
Chromosome 13 (position 24648860)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 24294520 |
GRCz11 | 13 | 24424970 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAAAGGGTGGTCATGTGACGAGGATACTATTTTTAACACTTCAGCTGAC[A/T]AACGCAGTCTGTCCAGTCCGCCCTCTGCTTTTCTGAGCCTGACAGCACCT
Long Flanking Sequence:
ATTTTCAGATTCACGAACAAACTTTTGTAAACAATTTTTTTTTAATTAAATCAGTCATTGAGATTTATGAATTTGTTTCAAACTTGCATGTGAAATCATTCAAACGATATTGTGATAGTGAAGACTGGAGTAACAACTGCTCAAAATCCATCATAGTCGTCATAGATAAAATTAAAAACATGAAAACAGTATTAAACTTTGACAATATTTCACAATAAATGCAACCTTGTTTTGTTCGAGTCTTCTTTCTTGTTTTCCAGGATTTCCTATTAACCATTTTCAACTTTTGTTGATTTACTCAGATCAGTTACAAAGCAGATACCTCTAAAGAAAAGGACAAAGGTCTACCCACGCAGCCATTCAGAAGTATTAAAGAAGTTTCTCCATGTTATAAATCCTCTCCACCATTATCAAAAGATGACCTTGATTCTTCCATGAACATGTCGGACCTCAAAGGGTGGTCATGTGACGAGGATACTATTTTTAACACTTCAGCTGAC[A/T]AACGCAGTCTGTCCAGTCCGCCCTCTGCTTTTCTGAGCCTGACAGCACCTCTAGTGCCTAAGTGGACATCAAGTCCTAAAAGCACTTCTCGCATGTCCAATCATATGTCTCATTTGAAGACAAATGTAAGAACTAGAGCAGGTGAGATTATGGATAGAGGAAGAGATTCTCTTATTAACACCGGATCTTCTCAGTATTATAATAAGAATCATCCACATGGGTTCAAACACATGTCAGCTTACCAGACCAACTATTGGGCCTGTGCCATCCCCAGCTCCATGCCACCATCCCCAAACCGCAAATCCCCAAGCTGGGACCCTGACAAGGAATACCAAGAGCTCTTGGACTACACGTACCCTCTGAGACCCAACATGAACAGCACATGGAGATCATCAGCGGTGGATCATCACTTGAGAACCGATCCGCTGTTACAAGACTCAGGCATAGAGTTGGACCGCTTTTGCAGCTCTTCCAGCTTGTCTTGCTTAGATCTGTCCTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35481
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:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000057588 | Nonsense | 389 | 650 | 3 | 6 |
ENSDART00000125949 | Nonsense | 389 | 685 | 2 | 6 |
ENSDART00000147514 | None | None | 126 | None | 4 |
Genomic Location (Zv9):
Chromosome 13 (position 24648183)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 24293843 |
GRCz11 | 13 | 24424293 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGGTTGTCCTTTGAAAGCCTTGACTGTGATGCAAAGTCAAGGGGTCACTA[T/G]CGCAAATGGGGTGTCTTTTCGACATATGGATCTGCCCCTACTTTTATTAG
Long Flanking Sequence:
AACACCGGATCTTCTCAGTATTATAATAAGAATCATCCACATGGGTTCAAACACATGTCAGCTTACCAGACCAACTATTGGGCCTGTGCCATCCCCAGCTCCATGCCACCATCCCCAAACCGCAAATCCCCAAGCTGGGACCCTGACAAGGAATACCAAGAGCTCTTGGACTACACGTACCCTCTGAGACCCAACATGAACAGCACATGGAGATCATCAGCGGTGGATCATCACTTGAGAACCGATCCGCTGTTACAAGACTCAGGCATAGAGTTGGACCGCTTTTGCAGCTCTTCCAGCTTGTCTTGCTTAGATCTGTCCTATACAGGGACTCGGCGACGTAGCCCAAGAACAAGCCAAAAGCTTGAATTTCGACCTCTAAACCAATCACATTCAAAGTCCTCAGATGGCATCCTGTCCAGTAGTCTATACTCCTCAATTGACAAAGTTGGGTTGTCCTTTGAAAGCCTTGACTGTGATGCAAAGTCAAGGGGTCACTA[T/G]CGCAAATGGGGTGTCTTTTCGACATATGGATCTGCCCCTACTTTTATTAGATCAACACGCATCCTTCCCCGTCCTTTTTTGCAGGATGATTTAGACGAAGAGTTTCTTCGCCTACCAGATCAGCTACAGGAACTTCAGGAGCTTTCACAGCAGCTGAGGGACATTAGTGACCACATGAGCCAACCGGTCATCACTAGCTGGGAATCTCTGGAGAGCGAGATGACCTCCGTCAGATCACCAACGGTTCAAGGAATGCAGGAACCATTGGTGGAAGAAAAGTGTGATGAAAATCCTAGATCCCAGAGAGAATCTGTTCCTGATGTTCCTCTCACACACCAGGACCATTTACTGAAAACAGAGGAACCTCCTACCAGTATCCAGATGATTAGCCAAGACTTGAATAGGAACAACTTGAGGGAAGTGGAAGCTATTATGGATCAGCTGAGGGGGTTGTCAGTATCTGAGCTTCAGGGGACAATGCAAACAGATGAAAATGAGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44786
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000057588 | Nonsense | 392 | 650 | 3 | 6 |
ENSDART00000125949 | Nonsense | 392 | 685 | 2 | 6 |
ENSDART00000147514 | None | None | 126 | None | 4 |
Genomic Location (Zv9):
Chromosome 13 (position 24648175)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 24293835 |
GRCz11 | 13 | 24424285 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTTGAAAGCCTTGACTGTGATGCAAAGTCAAGGGGTCACTATCGCAAAT[G/A]GGGTGTCTTTTCGACATATGGATCTGCCCCTACTTTTATTAGATCAACAC
Long Flanking Sequence:
ATCTTCTCAGTATTATAATAAGAATCATCCACATGGGTTCAAACACATGTCAGCTTACCAGACCAACTATTGGGCCTGTGCCATCCCCAGCTCCATGCCACCATCCCCAAACCGCAAATCCCCAAGCTGGGACCCTGACAAGGAATACCAAGAGCTCTTGGACTACACGTACCCTCTGAGACCCAACATGAACAGCACATGGAGATCATCAGCGGTGGATCATCACTTGAGAACCGATCCGCTGTTACAAGACTCAGGCATAGAGTTGGACCGCTTTTGCAGCTCTTCCAGCTTGTCTTGCTTAGATCTGTCCTATACAGGGACTCGGCGACGTAGCCCAAGAACAAGCCAAAAGCTTGAATTTCGACCTCTAAACCAATCACATTCAAAGTCCTCAGATGGCATCCTGTCCAGTAGTCTATACTCCTCAATTGACAAAGTTGGGTTGTCCTTTGAAAGCCTTGACTGTGATGCAAAGTCAAGGGGTCACTATCGCAAAT[G/A]GGGTGTCTTTTCGACATATGGATCTGCCCCTACTTTTATTAGATCAACACGCATCCTTCCCCGTCCTTTTTTGCAGGATGATTTAGACGAAGAGTTTCTTCGCCTACCAGATCAGCTACAGGAACTTCAGGAGCTTTCACAGCAGCTGAGGGACATTAGTGACCACATGAGCCAACCGGTCATCACTAGCTGGGAATCTCTGGAGAGCGAGATGACCTCCGTCAGATCACCAACGGTTCAAGGAATGCAGGAACCATTGGTGGAAGAAAAGTGTGATGAAAATCCTAGATCCCAGAGAGAATCTGTTCCTGATGTTCCTCTCACACACCAGGACCATTTACTGAAAACAGAGGAACCTCCTACCAGTATCCAGATGATTAGCCAAGACTTGAATAGGAACAACTTGAGGGAAGTGGAAGCTATTATGGATCAGCTGAGGGGGTTGTCAGTATCTGAGCTTCAGGGGACAATGCAAACAGATGAAAATGAGACCAAAGAGT
Associated Phenotype:
Not determined