ZMP
ctbp1
Ensembl ID:
ZFIN ID:
Description:
C-terminal binding protein 1 [Source:RefSeq peptide;Acc:NP_571789]
Human Orthologue:
CTBP1
Human Description:
C-terminal binding protein 1 [Source:HGNC Symbol;Acc:2494]
Mouse Orthologue:
Ctbp1
Mouse Description:
C-terminal binding protein 1 Gene [Source:MGI Symbol;Acc:MGI:1201685]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa19082 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa197 | Nonsense | Available for shipment | Available now |
sa35683 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa19082
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079583 | Essential Splice Site | None | 449 | 2 | 11 |
ENSDART00000122739 | None | None | 449 | None | 9 |
ENSDART00000144367 | None | None | 288 | None | 6 |
Genomic Location (Zv9):
Chromosome 14 (position 22824514)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 21524002 |
GRCz11 | 14 | 21821247 |
KASP Assay ID:
2261-7170.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAAAGACTGTGACGTCAGCAGAGTGGTTGATTGGCTTTGACATCATCAAG[T/C]AGGTGGTTGCATTATTATTATTATTATTATTATTATTTTCAGTCATCTCT
Long Flanking Sequence:
TTTAACTTAGTTTTCCTGCGCTGGACTACACAACACAACCACAGAGATGTTTAGAAAGAAAATAGATGAAGAAGTTTTAACTTTGTGATTCTTTACTTGTCTCATACTTCAAATAAGCCATCAAAACGTACCTACTAAACAGTACTGTTTATTAAACACGTTTATCTGCCTCCTCTGATTGTTTTATTTGGATATCTAATGGTGCAAAATGTAACTGGAGTGGTTTTAAAAACTTGTTTTAAACGGTCGTTTGGAGTGTTTGAGGCGCTACAACATCAATGCATGTGAAATGGGCGTTATTTCTATTGCGAGCACACAAGACTTACAATTTCGTGTATTAAGAAAAAGTATTTAAATGTCTGTGCATTCTTTTGATTTTGACTTAATTCCATCTTCATGGTCTGTTCTCTGTCATAAATAATGTTTAATTTCCCCCTTCAGCTGCCATTGTAAAGACTGTGACGTCAGCAGAGTGGTTGATTGGCTTTGACATCATCAAG[T/C]AGGTGGTTGCATTATTATTATTATTATTATTATTATTTTCAGTCATCTCTATTTTTACAAATCTGTCATATATGTGGGTGAACGAGCCTCACAGTGTAACTTCACAAACAGGTAGTTGTGTGTTACACCAGATGAAAATGTGCATGTTATTTTTACATGATTATTAGATCAGAGTAGGCATGGGCTGATATAAGATTCTGACGGTATGATAAGTTTGACGGTATTTTGATTACTGCTATAAAATATATTCTTTTTAAATGTCTGGGTAAAAAACTACTTTTTCCACTTTTTTATATTAGAAAACATTTACAATATTTTGGAGCAGTAAACATGTCGGGCTAAATCAAATGAATCATTGACTTCTGCTGTCTTCATTAGTTTCCAGAACACAGATTCCAATACAATTCACAGGGTTTATTCGATCTTTGAAAAACCTGGAGAAGTCATGGAATTTTGACATGGCATTTTCCAGGCCTGGAGAAGTTTTGGAAAAACAGAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa197
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079583 | Nonsense | 60 | 449 | 4 | 11 |
ENSDART00000122739 | Nonsense | 60 | 449 | 2 | 9 |
ENSDART00000144367 | Nonsense | 44 | 288 | 2 | 6 |
Genomic Location (Zv9):
Chromosome 14 (position 22837679)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 21537167 |
GRCz11 | 14 | 21834412 |
KASP Assay ID:
554-0109.1 (used for ordering genotyping assays)
KASP Sequence:
TGTACAGTGGAGATGCCCATCCTGAAGGACGTGGCCACTGTGGCTTTCTG[C/A]GATGCCCAGTCCACCCAGGAGATCCATGAGAAGGTATCGTCATAAGGATT
Long Flanking Sequence:
TCACTTGTTCCAAACATGGAGTTTTTATTTTGTTGATTGCAAAACAGGATATTTTGAAGAAAGCTGGAAACCTGTAACCATTGACTGCCATAGTAGGAAAAACAATAGCTTCCAGCTTGCTTCAAAATATCTGGTTTTGTGCTCAAAAGTAGAAAGAAACTCGGTTTATAACCAATTGAGGATGAGCAAATACAATTTTGGAGTGAACTGTCTCCATTGCTAGTTTACAAAACTCCTGGTTTACTACTGTGATTTTTAAAATGTTTGCTTGTAGGTGTATGCAAAGGATTCATTTGTGTTTTCTGATGTCACCAGAACTGTACTTAATTGAAAGCTGTTTGAGTTTCCTGTAAATTAAAGAATTTTTGGTGCCCTGCAGGCATTCGACCACCCATCCTCAATGGCCCAATGCACCCTCGTCCTCTGGTGGCGCTGCTGGATGGACGGGACTGTACAGTGGAGATGCCCATCCTGAAGGACGTGGCCACTGTGGCTTTCTG[C/A]GATGCCCAGTCCACCCAGGAGATCCATGAGAAGGTATCGTCATAAGGATTTTTCCATGTTCATTACAGTCAGCTTTAATACAGTGAGTTTCATGAGGCTTTCGTGCTGTAGGTCTTAAATGAGGCTGTTGCTGCTCTGCTCTACCACACCATTACACTGTCACGAGATGACCTGGACAAATTCAAAGGCCTCAGGGTCATTGTGAGGATCGGTAGTGGGTTCGACAACGTTGATATTAAAGCAGCAGCAGAGCTTGGTAAGTTTTGTTCTTGCGTTATGAAAGAATCTTGTTGGATTGAATGAGTTTTAGTCAAACTGGATCTGTGTCTTCAACAGGTATTGCAGTGTGTAATGTGCCAGCTGCATCTGTGGAGGAGACGGCAGACACTGCCATGTGTCTAATTCTGAATCTGTACCGCCGCGTCACTTGGATGCATCAGGCACTGCGTGAAGGCACCCGAGCCTCCAGCGTGGAGCAGATCCGGGAAGTAGCCGGAGGC
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa35683
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 |
---|---|---|---|---|---|
ENSDART00000079583 | Nonsense | 179 | 449 | 6 | 11 |
ENSDART00000122739 | Nonsense | 179 | 449 | 4 | 9 |
ENSDART00000144367 | Nonsense | 163 | 288 | 4 | 6 |
Genomic Location (Zv9):
Chromosome 14 (position 22838192)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 21537680 |
GRCz11 | 14 | 21834925 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTCCAGCGTGGAGCAGATCCGGGAAGTAGCCGGAGGCGCAGCACGTATT[C/T]GAGGAGAAACGCTGGGCATCATTGGGCTGGGTGAGTCCTGATGTGATTTA
Long Flanking Sequence:
ACCCAGGAGATCCATGAGAAGGTATCGTCATAAGGATTTTTCCATGTTCATTACAGTCAGCTTTAATACAGTGAGTTTCATGAGGCTTTCGTGCTGTAGGTCTTAAATGAGGCTGTTGCTGCTCTGCTCTACCACACCATTACACTGTCACGAGATGACCTGGACAAATTCAAAGGCCTCAGGGTCATTGTGAGGATCGGTAGTGGGTTCGACAACGTTGATATTAAAGCAGCAGCAGAGCTTGGTAAGTTTTGTTCTTGCGTTATGAAAGAATCTTGTTGGATTGAATGAGTTTTAGTCAAACTGGATCTGTGTCTTCAACAGGTATTGCAGTGTGTAATGTGCCAGCTGCATCTGTGGAGGAGACGGCAGACACTGCCATGTGTCTAATTCTGAATCTGTACCGCCGCGTCACTTGGATGCATCAGGCACTGCGTGAAGGCACCCGAGCCTCCAGCGTGGAGCAGATCCGGGAAGTAGCCGGAGGCGCAGCACGTATT[C/T]GAGGAGAAACGCTGGGCATCATTGGGCTGGGTGAGTCCTGATGTGATTTAATCAGAGGGCACCATGAATCAGTGCTGGAAGGAGAATTAGATCAGTTAAGCAGACAGCTGACAGCACATTTACACTGCATATGTAGAATTACTAGAGTACAAGTTTTAACTTGGTATGATATTGTCATGATAGTATTATCTAAATATTTCACTATATAAAGAGATTTAAGACGCATAACTATTCTTTCTATCCTGATTAAGATTTTAATCTTGTTTTTAGTTTTAACACTGAATTGTTGACATCTGTTTATGCCTTCAGGTTAATTTTAATTAATTGAGCTTAATCCATTTAAAAGGCCAGTTTTTCTAGTTTTATTTCATACTGAGCCAGAAATCTGTTTCACCACTTCCAAGACACCAAAATGTTAGTTTTATTCTTTTTTACATTTCTGGAGTTTTTACAAAGGGTTTGTTTATTTATTGATCAAACCCATATGATTTTAAAAACAT
Associated Phenotype:
Not determined