ZMP
si:dkey-230e6.2
Ensembl ID:
ZFIN ID:
Human Orthologue:
CNOT4
Human Description:
CCR4-NOT transcription complex, subunit 4 [Source:HGNC Symbol;Acc:7880]
Mouse Orthologue:
Cnot4
Mouse Description:
CCR4-NOT transcription complex, subunit 4 Gene [Source:MGI Symbol;Acc:MGI:1859026]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa44291 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa13605 | Essential Splice Site | Available for shipment | Available now |
sa39482 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa44290 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa44291
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 |
---|---|---|---|---|---|
ENSDART00000034714 | Nonsense | 131 | 772 | 3 | 12 |
ENSDART00000140182 | None | None | 31 | None | 2 |
Genomic Location (Zv9):
Chromosome 25 (position 20506491)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 19917392 |
GRCz11 | 25 | 20015046 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCTCTCTCTCTCTCTTAATCGTTTCTTAGGTTCTAAAGCGTCCAGAGTA[T/A]TTTGGCAAGTTTGGAAAAATTCATAAAGTGGTCATCAATAACAGCACGTC
Long Flanking Sequence:
AAATTCTGATATGCAGATTTGATGCTAAGAAATGTTTTGCTATTATAAATGTTAATTACTGATTACAAATCCTGTTGTGTTGCTTACTTTTAGTGCAAATTAAAACCAGAATTAAATTTATTTAAATTTTTTATTTTTTTTTAAAACAAATTTAATGTTAATGAATAACTTTTCATGTCACTGTTTTAACAATAATACATTTAATCACTGTGTATGTTTATTAAAGTTACTAAACACCTAAATCATATCTGTAAATAGTGTCACTTTCTGTGGTAGGTAAAAAAGAATAGCTCAAAAATAGTGTTTTCATCAGTGAGTCGTTTGCGATTTGCTGAAAAATAGGAAATTCCCTCCCTCAGAGTGATTTCACACTTTGATTGTGTGATAAGTGGCCGAACCTCACCGTTGTGTCTGTTTTGTCATTCATGCAATAATTCACCTCCATAATCTCTCTCTCTCTCTCTCTTAATCGTTTCTTAGGTTCTAAAGCGTCCAGAGTA[T/A]TTTGGCAAGTTTGGAAAAATTCATAAAGTGGTCATCAATAACAGCACGTCATATGCAGGTTCACAGGTAGGAAAAGCTCTCCTTTTTGCTAGCCTGATGCACACAACTCATTAAAGGAACCCTCCACTTTTTTGCTGATAGAGTTAAACATTTGAGTTTTACCACTGGCAGGAGTACTTTTAGCTTAGCATAAATCATTCATTCGAATTAGACCATTAGCATGCTAAAAAAACACTTGATAAATAAAAAAAAAAAAAAAAAGCTAAAGTCTTTTGTGTTAAAATGATGGGATTTTTTTGTTGTTGCTTTTTTCCTAGTCTGATATGGCTAGGAACTATACTCTCATTTTGACATAAAAAATCAAGTAACTTTTGGCTGCAAAATCTACCATGGCTGTAGCAGGTGAAGTAATGTTGTGATGTACTACTGAAAACTTAAGCTTTAAGTAGGAGATTTATCAAATTTGTGATTTTCACAACGGTCTAACCCGATTCAATGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13605
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000034714 | Essential Splice Site | 187 | 772 | 4 | 12 |
ENSDART00000140182 | None | None | 31 | None | 2 |
Genomic Location (Zv9):
Chromosome 25 (position 20505227)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 19916128 |
GRCz11 | 25 | 20013782 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGYAATACAATGTGTAAACAATGTCATAGTGGACGGTAGAACGCTCAAG[G/A]TAAGTGCTAAGYCATCAGAATTTGATCTGTTTACAYARTATTTTCACGTC
Long Flanking Sequence:
GCTGTTTTATTCCAACATTCTTCAGTAAATCTTCATTTGTGTTTAAGAGAAAAAACAAATTTAAACGGGATTTGGAACAATCAAATGAGTTAAAAAAAACAAGAGTAAATGATGACAGAATAACATTTTGGGGGTTAAACTATTATCTTAAAGGCTGATTTATACTTCTGCATCAAGTGTATTTGTACGCTTCTCACGCATTTCCCTCACCGTGTTCAAGATAAGTAACTACACGTCAAAACAACATGTAGCGCAAGCTCTGTGATTGGTCGGCTTGGTATGCACTGTGGATCACGCTGATCACTCGATGCAAAAAAATAAACCAGCCTTTAGGCTACAGCAAAACAGTCGAGTTACGAAAACGTTTGTATTTTTTATTATTTTTTTTGTCTCCACAGGGTCCTAGTGCTAGTGCCTATGTAACTTACATTCGTTCAGAGGATGCCCTTAGAGCAATACAATGTGTAAACAATGTCATAGTGGACGGTAGAACGCTCAAG[G/A]TAAGTGCTAAGTCATCAGAATTTGATCTGTTTACACAGTATTTTCACGTCAGGGCTCCAGACAGCAAGTAAATGGATGTATTATGCAATTTTTGTTCATTTTGTTGGCGGTTTTAACTGGTGCTACTAGCAATGTGCCTTGTCTGTTGCATCTGTAAAACATTAAACATCTGAAGGAGAACAAAGCAGCAGTACTCGACTTGTTTGAACCAATTTTAAGCTAACTGCGAATGTTTAATTGCTGACTAATCTTGAGTTTACCACATGGTTCCAGTCACAAACCGCTAATGTCAGATTAAGATAATTTTTTTATATATATATATAAAAGGATTAAATTAGATTAAAAAAAGTTTGAAGTGAGATTAATGTCTATGACATTCTCCGCAGCACTGATGCAGAAAAACAAGAGAAGCCTTGTTTCAGACCACTATTGATCAACATTTACTATGGGTTGCTAGTAGCAGTGTAACTGTAAACATGATAATATGGTAGAAATGCAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39482
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000034714 | Nonsense | 227 | 772 | 5 | 12 |
ENSDART00000140182 | None | None | 31 | None | 2 |
Genomic Location (Zv9):
Chromosome 25 (position 20503894)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 19914795 |
GRCz11 | 25 | 20012449 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCATGTATTTACATGAACTTGGCGATGAGGCAGCTAGTTTTACAAAAGAA[G/T]AAATGCAGGTGAGGGTGCATGTTTACACCTGATAACTTCAAAGCAGAAAT
Long Flanking Sequence:
TCAGAGTTAAGAGTTGTGTGTGTGGTTATAAAAGGTTTTAGTCAACAATAATAGCCCTGATTTATACTTGACATTTTATTTTTATTTTAAATAAAAAAATACATTTAGAAACCATATAGACGCTACTTAAATCATGGTCATGTAGTTCTTTTGGTTGTCATGATCCACAAACGTAGAGATTGTTAAAATCTGCCCAATCTGTGCGAATTTACATCTGCATCCCACAATTCAAGCTCTCGATTCTGTCAAATTATTAATATTACACGATACATCTGTAGACATTATTCTGGAGCTCTGTTTATTATGTTAGTGATCAATATTTATTTGATCATTCTGTCACCTTTTGATGTTGATAGTCATTGTGTCTCTTGCTTTGTTTGAAGGCTTCATTAGGTACAACAAAGTACTGCAGCTACTTTCTTAAAAGCATGCAGTGTCCTAAACCAGACTGCATGTATTTACATGAACTTGGCGATGAGGCAGCTAGTTTTACAAAAGAA[G/T]AAATGCAGGTGAGGGTGCATGTTTACACCTGATAACTTCAAAGCAGAAATTGAATTTGTATGTCTGATTTTGTTGTTTAACTACTATGTATTGTTTTTGTCAGGCTGGGAAACATCAAGAATATGAACAAAAGTTACTCCAAGACCTTTACAAAGCAAACCCCACCTTTTTACTAACCTCAACATGTGGGGAGAAGTCAAAGAGCAAATCCAATTCCACTCAGCGGTGTGTTTTTGTTTTTTGTTTTTTCTTAATCTCACATGCTCAATTAGACACCCTTATTTTTCAGTTATTGTATTGTCTTAATGTTTAGCCTGATTATATTTTCTATCTTTCAAATGATTTCATTTCCAGGCCCAATAGCACCAATAAAGAAGGATGGCCCTCATTACAGAATTATGGGAAAATGGTGAACGGTTTAACCACAGAGCATCGTAAGTCTCCTCCTCTATTAGACTGCCTAACAGACTCCGATCACATGACTCCAGACGAACCAGACC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44290
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 |
---|---|---|---|---|---|
ENSDART00000034714 | Nonsense | 229 | 772 | 5 | 12 |
ENSDART00000140182 | None | None | 31 | None | 2 |
Genomic Location (Zv9):
Chromosome 25 (position 20503888)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 19914789 |
GRCz11 | 25 | 20012443 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTTACATGAACTTGGCGATGAGGCAGCTAGTTTTACAAAAGAAGAAATG[C/T]AGGTGAGGGTGCATGTTTACACCTGATAACTTCAAAGCAGAAATTGAATT
Long Flanking Sequence:
TTAAGAGTTGTGTGTGTGGTTATAAAAGGTTTTAGTCAACAATAATAGCCCTGATTTATACTTGACATTTTATTTTTATTTTAAATAAAAAAATACATTTAGAAACCATATAGACGCTACTTAAATCATGGTCATGTAGTTCTTTTGGTTGTCATGATCCACAAACGTAGAGATTGTTAAAATCTGCCCAATCTGTGCGAATTTACATCTGCATCCCACAATTCAAGCTCTCGATTCTGTCAAATTATTAATATTACACGATACATCTGTAGACATTATTCTGGAGCTCTGTTTATTATGTTAGTGATCAATATTTATTTGATCATTCTGTCACCTTTTGATGTTGATAGTCATTGTGTCTCTTGCTTTGTTTGAAGGCTTCATTAGGTACAACAAAGTACTGCAGCTACTTTCTTAAAAGCATGCAGTGTCCTAAACCAGACTGCATGTATTTACATGAACTTGGCGATGAGGCAGCTAGTTTTACAAAAGAAGAAATG[C/T]AGGTGAGGGTGCATGTTTACACCTGATAACTTCAAAGCAGAAATTGAATTTGTATGTCTGATTTTGTTGTTTAACTACTATGTATTGTTTTTGTCAGGCTGGGAAACATCAAGAATATGAACAAAAGTTACTCCAAGACCTTTACAAAGCAAACCCCACCTTTTTACTAACCTCAACATGTGGGGAGAAGTCAAAGAGCAAATCCAATTCCACTCAGCGGTGTGTTTTTGTTTTTTGTTTTTTCTTAATCTCACATGCTCAATTAGACACCCTTATTTTTCAGTTATTGTATTGTCTTAATGTTTAGCCTGATTATATTTTCTATCTTTCAAATGATTTCATTTCCAGGCCCAATAGCACCAATAAAGAAGGATGGCCCTCATTACAGAATTATGGGAAAATGGTGAACGGTTTAACCACAGAGCATCGTAAGTCTCCTCCTCTATTAGACTGCCTAACAGACTCCGATCACATGACTCCAGACGAACCAGACCTTGAAC
Associated Phenotype:
Not determined