ZMP
cpeb3
Ensembl ID:
ZFIN ID:
Description:
cytoplasmic polyadenylation element-binding protein 3 [Source:RefSeq peptide;Acc:NP_001161134]
Human Orthologue:
CPEB3
Human Description:
cytoplasmic polyadenylation element binding protein 3 [Source:HGNC Symbol;Acc:21746]
Mouse Orthologue:
Cpeb3
Mouse Description:
cytoplasmic polyadenylation element binding protein 3 Gene [Source:MGI Symbol;Acc:MGI:2443075]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa17508 | Essential Splice Site | Available for shipment | Available now |
sa42284 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa12175 | Nonsense | Available for shipment | Available now |
sa6328 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa17508
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000084354 | Essential Splice Site | 231 | 586 | 1 | 10 |
Genomic Location (Zv9):
Chromosome 13 (position 43060679)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 42281638 |
GRCz11 | 13 | 42407698 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCCAGAGCCCTTCAGAACTGACAACAGCAACAACATGCTGCCATTTCAGG[T/A]GAGATTCTTCACTTCATCAATAGASGTAAWGCNNATAGGGCTGAGGTAAAGT
Long Flanking Sequence:
CTCTCTCTCTCCGTCGTTCGGCAGCACTTGGTCCACCAACACCGTGGACGAGGGCTTTTTCCAAGGGATTCCGTCTGTGAACGGAACGATGCTTTTTCAGAACTTTCCCCATCACGTCAACCCGGTGTACGGTGGGAATTTCTCCCCGCAGATGAGAAGGTCTCCGCTGGGAGTGAACCAGAGAAACCCCTACAGTCACCAGACCCTAATTAATAAAGTTGCCGCCTCGTCCGCGTCCTCGTCCGCCTGGAATAACCACCAGAACGCGGTGTGGAGCTCCGCGGCGAACCCGTGGAGCGGCAGAGACCCGCGGAGAGGGCTCGGGCTGAGCGTCCCGTCTCCGCTCAACCCCATCTCCCCGACCAAAAAGCCCTTCCCGAGCACTGTTATCGCGCCCCCGAAATACCAGAGACCCGGAGCACTGCAGAAACCCTGGATGATCTCAGATCCTCCAGAGCCCTTCAGAACTGACAACAGCAACAACATGCTGCCATTTCAGG[T/A]GAGATTCTTCACTTCATCAATAGAGGTAATGCATAGGGCTGAGGTAAAGTTGGTTTTATATTCGCGCATTCCGACTTTCTCCTTAATAATATAGTCTATAATTTCAGAGCATGTTCTTTACAGATAAATAGTGAAATTGTTTTAGCAGCCAATTAGTATGAAAGTAGGCTACAACATTGTTCACAGTCAAATAGCTTAAATAGTGTTGTCTTGAAGGCACTTGCGTGCGATTTCAGACCGAATATTCAAAGTATGTGCGAATATAAAACCAACTTTCAACCTCAATAGCAAAGCGAAATTTTGTGTTGGTAGACTGATAGTACGAAAAAATGTGTTCATTCAAGTATAAAATGTTTTGAATTACAATTTGAACACACAGAACACACATTTAATTGTGGTAAAAAGTTTATAAAGGCATAGCCTAAAACGTAATTTATAGACGTATTTCTTTATGATAATCATAAAATAGTTCATTGACATTAAAAAAACTCCCTAAATAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42284
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 |
---|---|---|---|---|---|
ENSDART00000084354 | Essential Splice Site | 232 | 586 | 2 | 10 |
Genomic Location (Zv9):
Chromosome 13 (position 43067434)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 42288393 |
GRCz11 | 13 | 42414453 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGACACATCTTTCACCTGTGACCTTTAACACCTTTCCTTTTGTCTTTCA[G/A]GATCGAAATCGACCCTTCGACCCCTTCAACTTGCAGACTTTGGAAAACTC
Long Flanking Sequence:
CAAGGAGGCTAAAGACCATGGCCTCTAGGAGTGAGGTTTACTTGCACAGCACTTACTAGCTGGCCTCCGTTACACATGTGTGCGTGTGTGCCCATTTATAACATTATTTTGCGTGTAGAGGACACTCGCTACCATTTCTGGAACCTGTACTATGACGCTGGATTAGCTGGCTAGCCAGTTAACTTTCAGTTTAGTTTGCATCAGTCTTTGGTTTTAGGTATCATGAAGGCAGCTCAATGTAATCACTCTTTGTTGCCATGATTTTATAAAGCAGCTGATCCGAGCTGCATTCATGGTACCTAAAACCCAGAATTGTTGTAAACTAAACTGAAACCTTACTGGCTAGCCTGCTAATGTGGCTTTATGGTACTGTTGTTTAGCTTGTGTTTTTGTTTATTGGATCAAAAATGATTGACTCTAATTAGAAAGGCTGTGAAATGGTGGTGCAGTGTGACACATCTTTCACCTGTGACCTTTAACACCTTTCCTTTTGTCTTTCA[G/A]GATCGAAATCGACCCTTCGACCCCTTCAACTTGCAGACTTTGGAAAACTCTCTAATGGACATGATTAAGAACGACCATGACAAAGGTAAACACCACCCTGCCGCTGGTCCACCAATGACTATCGCTGATATTTTATGGAGGAATCATTTTGCAGGTTAGGACTGTTTAAACATCCACCCTTCTGTGCTCTTTTGGCGTCAGATTTTTCAAAGCATTTGATTACCTGTTTGTATTTTTATGTTTATTTAAATAACTGATGTTCTGTTCATTCTAAATAAAAATAATAAGTATATTATATTATTTGCAATTATACATTATATAATAATATTATATTATAATATATAGTAGTATTGTAAAATAATATCGTTCAAAAGATAATGTTAATGCTTCATATATGTTTATATATGTATATTTTATTCATATATTATAGAGTATGAGTATTTATTTATTTATTTTTTAGATTTTAATACTTTTATTTAGCAAGTATACATTAAAGCTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12175
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 |
---|---|---|---|---|---|
ENSDART00000084354 | Nonsense | 275 | 586 | 3 | 10 |
Genomic Location (Zv9):
Chromosome 13 (position 43083981)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 42304940 |
GRCz11 | 13 | 42431000 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTAGRTCGCATGGGTCTCAACTTTCACCATCCAGTAGCTGAACATATAT[T/G]ACCACTRAACAGTGAGTATCTCTCTTTAACTGTGATATTAATGCTGTGTT
Long Flanking Sequence:
AACTAGGTTAATTAGGTTAACTAGGCAGGTTAGGTTAATTAGACAAGTTATTTTATAATGATGGTTTGTTCTGTAGACTGTCGAAAAAATATAGCTTAAAGGGGCTAATAATTTTGTCCTAAAAATATATACACACACTCGTAGATGTGTATGTGTTTGAGATCAACTGTAGACATGCCTAAGACACAATTCCAACACATGTTGCCAATGCAAGTCTACAGTAGTTGGAATTTGGTTGATTTTAGTTCAGGTCTGTTATCTTCAAAGGCATCAGCATTTCAAAAAACAACTTTCAGCCTAATATGCATTAAAAAATAAATTGGATCTTATTTATTTATTATTAATCTTTTCTTTTTTTTCTTTTTTTTTTGGAGAATTGGCCATAACTATTCTTGTTTTAAATTTGTTTTGCATTAAATCATATGTTTTAATGGTGTCTTCTTATCTCCTTGTAGGTCGCATGGGTCTCAACTTTCACCATCCAGTAGCTGAACATATAT[T/G]ACCACTAAACAGTGAGTATCTCTCTTTAACTGTGATATTAATGCTGTGTTCATTTTTAAAGGTAGCACATCATTGGTTTTTCCCTTTATTTCAATCAGTCAAATCAGTTCAGTGAACAACACTGTTTTTGAATGAAGCATGTCCTTAAAACGTCAAATATTTATGATTTTTAAATGAACAAATTTTACAATTTTCATTTTCATTTTCATTTATTTACAAATTTCAACATTATTACTCCAGTTTCAGTTCCATAAGAAATCATTATAATATGGTTTTTGCAAACATTTCTTTTAATTATCAATGTTGAAAATTATTTTTGGTTTTTATGATGAATATAAAAAAGTTTTAAAAGAACAGTATTTAGAAATCCTTTGTAGCCATTAAATCATGTTGATACACTTTTGCTAATTGATTATTGTTATTTATTATTATCATCATCATCATTATCATCATCATTTAATATTTATTTTTTATTTTTTATAATTATAAATATATAAGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6328
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000084354 | Nonsense | 517 | 586 | 10 | 10 |
Genomic Location (Zv9):
Chromosome 13 (position 43124831)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 42345790 |
GRCz11 | 13 | 42471850 |
KASP Assay ID:
554-4694.1 (used for ordering genotyping assays)
KASP Sequence:
CGCWTAAACCAGTGAATTTYTGTGTGTGCACAGGTGGAGGTGAAGCCGTA[T/A]GTTCTGGATGATCAGATGTGTGATGAATGTCAGGGMTCTCGTTGYGGAGG
Long Flanking Sequence:
ACACTGTATATTCTACAATAAAAGTCCTTATCACACTGTATATTCTACAATAAAAGTCCTCATCATACTGTATTTTCTGCAATAAAAGTCCTCATCACACTGTTTATTCTACAATAAAAGTACTCATCATACTGTATTTTCTACAATAAAAGTCCTCGTCATACTGTATTTTCTATAATAAAAGTCCTCGCCATACTGTATATTGTACAATAAAAGTACTCATACGTATATTCTACAATAAAAGTCCTCGTCATTCTGTATATTCTACAATAAGTTCTCATAATACTCTATTTTCTACAATAAAAGTCCTTGTCATACTGTATATTCTACATTAAAGACCCTTGTCATACTGTATATTCTACAATAAAAGTCCTCATCATAGTGTATATTTTACAATAAAAATCCTTATCATACTGTATATTCTACAATAAAAGTCCTCATTATTTCAGACGCTTAAACCAGTGAATTTCTGTGTGTGCACAGGTGGAGGTGAAGCCGTA[T/A]GTTCTGGATGATCAGATGTGTGATGAATGTCAGGGATCTCGTTGTGGAGGGAAGTTTGCCCCTTTTTTCTGTGCCAACGTGACGTGTCTGCAGTATTACTGCGAGTACTGCTGGGCGAGCATCCACTCGCGGGCCGGCCGAGAGTTTCACAAACCGCTGGTGAAGGAGGGCGGGGATCGACCCAGACACGTGTCCTTCCGCTGGAGCTGATGAACACCGCAACATCGCCCTCTCCACCACAAACACATCACATCTCTGTCCGCTCTGCTTAACAACCTTAGGAAAAGATGAATTGTTGAGTCTGCGTGCTCAAACGTTGCACTTTGGCACAAACAGTCGATGTTAACGCTTATCAGGGTGTTGTGCTGTTAATTCGCTCATTTTCCTCTGTTTGATCAGTTTAGTGCTCCATATTGGTAACATTAGGCAGTGTGAGACTATATATATATATATATATATATAATATATACATTTACAAAAAGATCTATTTTTATTTTATA
Associated Phenotype:
Not determined