ZMP
crebbpa
Ensembl ID:
ZFIN ID:
Description:
CREB binding protein [Source:RefSeq peptide;Acc:NP_001082924]
Human Orthologue:
CREBBP
Human Description:
CREB binding protein [Source:HGNC Symbol;Acc:2348]
Mouse Orthologue:
Crebbp
Mouse Description:
CREB binding protein Gene [Source:MGI Symbol;Acc:MGI:1098280]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa9163 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa37532 | Nonsense | Available for shipment | Available now |
sa25181 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa32405 | Essential Splice Site | Available for shipment | Available now |
sa14981 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa9163
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 |
---|---|---|---|---|---|
ENSDART00000087250 | Nonsense | 253 | 2349 | 3 | 31 |
ENSDART00000148002 | Nonsense | 253 | 2312 | 3 | 31 |
Genomic Location (Zv9):
Chromosome 22 (position 27373185)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 26888630 |
GRCz11 | 22 | 26751082 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCATGGCAGGTGGCAACAGTCCATTTGGGCAGTACCAGGCTGGAGGTCAA[C/T]AACTGGGCACGAACGCACAGAATAAAGGCGCCCTTCCCAACAGCCTCCCC
Long Flanking Sequence:
AATTTAAAACAGCATCTTTGGATGTTTTTTTCTGCTGGAGATACTGCTCTAAAGAACTTTAAAAAAAGTAAATAAAAAATCTTACACGTACCTTCGGGACTGTATTACAGACAATTTTGGCCTTTTTAAAACCTTCACTTTTCTAAACCGCGGTATACCAAAACGGTTGTCGTCCCATGCCTAGTATATATTGAAATATCACAATGTCAGTTTATTCCAATATTGTGCAGCACTAGTTCCTACTTAGAATTACAAATATTTTACAAACATTTTTCTTTCGTTGCTGTGACCTTCTGTTTACCATTTATTCACAAAATATTGTGACGGAGTGCTAGGACATTCTCATGTTACAATTTTGTTTTGTGTCACTATAATGCTACAATTCATTTGTGTCACATCTTCTGTGGGCTCATGTGATCTAGTATGTTGTTTTCTTTGCTTTATAGATGGGCATGGCAGGTGGCAACAGTCCATTTGGGCAGTACCAGGCTGGAGGTCAA[C/T]AACTGGGCACGAACGCACAGAATAAAGGCGCCCTTCCCAACAGCCTCCCCCCATTTCCAACTGACCTAAAGGGGGCGACTGTCACCAGCGTGCCAAACATGGTGAGTTTCCCCATCACAATAACAAACTGATCAAAACCAACAGATGAAGAAGTTGATTCAACGACACTGTTGTTCTCTCGCCCACAGCCCCAGCAGCAGCAGGTGTCGGTGGGCATGGTGGCGGGTCAGGGCGTATCGACGGGTCCCACGGCTGACCCGGAGAAGCGTAAACTGATCCAGCAGCAGCTGGTTCTGCTGCTTCATGCCCACAAGTGCCAGCGGCGCGAGCAGGCCAACGGAGATGTGCGAGCATGTGCTCTGCCACACTGCAGGACCATGAAGAACGTCCTCAACCACATGACGCACTGCCAGGCTGGCAAGTCCTGCCAAGGTGAGTCCACATGCAGTGCCCACCACTGGACAGATAACAGAAGGCTTTTCCACATGAGCTTTAATCCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37532
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000087250 | Nonsense | 1221 | 2349 | 24 | 31 |
ENSDART00000148002 | Nonsense | 1184 | 2312 | 24 | 31 |
Genomic Location (Zv9):
Chromosome 22 (position 27406698)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 26922143 |
GRCz11 | 22 | 26784595 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCACTTTGTAACTCTTTTGAGCTAAATATTGTCATCTCGGATCCAGGGT[T/A]GCAGTCAACGAGGTTAGGCACTTACATAGAGGATCGAGTGAACAAGTACT
Long Flanking Sequence:
CTTTCAGCAGTGCTTCAGACTGAGCTGAGCCCAGTTTTAAGAACTGTTGTCCAGTGTCAGCAAGAGGATTTTCACTGGGCACACCAACAACAGGCGCTACATCATAATCGCGTCCCTACAAGAGAAAGCTTCTGATCAGTTAACGCAGCGTGAATGTCTGCAGAAGTTCAGATTTCGTCAAACAAGCAAAACAGTCAACTCACTCTGCTGCTTCATTCGCGCGAATCGCAGCGTTCGTGCCATCTTATTCATGTGAAACACGTCTGTGTGGATGTCTATTCGTGTTTTTGCATTAACATATTAAATCGGCAGCGCTTGATGCTTCATCCGCATCTGGTGTGAACGCAGAATTAGTGAATTGGAACAACTTGAAGGGAGAGTTATTACCTGAATTTTTATATTTGTGTGAACTAATCCTTCAAAAGTAGCATTATAAGTTTCATTAAAACTGTCACTTTGTAACTCTTTTGAGCTAAATATTGTCATCTCGGATCCAGGGT[T/A]GCAGTCAACGAGGTTAGGCACTTACATAGAGGATCGAGTGAACAAGTACTTGAAGAGGCAGAACCATCCGGAAGCTGGAGAGGTGTTTGTACGAGTAGTAGCCAGTTCAGACAAAACGGTGGAGGTCAAACCTGGCATGAAGGCCAAGTGAGTTTGCATTCATGCTTACCTCTTAATCTGCAGAGGACGCAAGTTTGGATGAAGAATCAATAAATGAGTTGGAATGATTGCTTTGTGTGTATGTGTAAAGGAAAGTATTACCATAGATTTGTTTGCCTGGTCAGAGTTTACCAGTATTGTTCATCAAACAAAATCTTGATTCTGTAGTGGTGTGCCAATGTTTGTGCTTTCAAAAGGTAAAGATGGCTTAATCCCCTGATTTGTTTCAGGTTTGTGGACACAGGAGAGATGATGGAGGCCTTCCCCTACAGAACCAAAGCACTTTTCGCCTTTGAGGAAATTGATGGAGTGGATGTGTGTTTTTTTGGCATGCACGTGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25181
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 |
---|---|---|---|---|---|
ENSDART00000087250 | Nonsense | 1252 | 2349 | 24 | 31 |
ENSDART00000148002 | Nonsense | 1215 | 2312 | 24 | 31 |
Genomic Location (Zv9):
Chromosome 22 (position 27406790)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 26922235 |
GRCz11 | 22 | 26784687 |
KASP Assay ID:
554-7889.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAAGTACTTGAAGAGGCAGAACCATCCGGAAGCTGGAGAGGTGTTTGTA[C/T]GAGTAGTAGCCAGTTCAGACAAAACGGTGGAGGTCAAACCTGGCATGAAG
Long Flanking Sequence:
GGCGCTACATCATAATCGCGTCCCTACAAGAGAAAGCTTCTGATCAGTTAACGCAGCGTGAATGTCTGCAGAAGTTCAGATTTCGTCAAACAAGCAAAACAGTCAACTCACTCTGCTGCTTCATTCGCGCGAATCGCAGCGTTCGTGCCATCTTATTCATGTGAAACACGTCTGTGTGGATGTCTATTCGTGTTTTTGCATTAACATATTAAATCGGCAGCGCTTGATGCTTCATCCGCATCTGGTGTGAACGCAGAATTAGTGAATTGGAACAACTTGAAGGGAGAGTTATTACCTGAATTTTTATATTTGTGTGAACTAATCCTTCAAAAGTAGCATTATAAGTTTCATTAAAACTGTCACTTTGTAACTCTTTTGAGCTAAATATTGTCATCTCGGATCCAGGGTTGCAGTCAACGAGGTTAGGCACTTACATAGAGGATCGAGTGAACAAGTACTTGAAGAGGCAGAACCATCCGGAAGCTGGAGAGGTGTTTGTA[C/T]GAGTAGTAGCCAGTTCAGACAAAACGGTGGAGGTCAAACCTGGCATGAAGGCCAAGTGAGTTTGCATTCATGCTTACCTCTTAATCTGCAGAGGACGCAAGTTTGGATGAAGAATCAATAAATGAGTTGGAATGATTGCTTTGTGTGTATGTGTAAAGGAAAGTATTACCATAGATTTGTTTGCCTGGTCAGAGTTTACCAGTATTGTTCATCAAACAAAATCTTGATTCTGTAGTGGTGTGCCAATGTTTGTGCTTTCAAAAGGTAAAGATGGCTTAATCCCCTGATTTGTTTCAGGTTTGTGGACACAGGAGAGATGATGGAGGCCTTCCCCTACAGAACCAAAGCACTTTTCGCCTTTGAGGAAATTGATGGAGTGGATGTGTGTTTTTTTGGCATGCACGTGCAAGAATACGGCTCTGATTGCCCTTTCCCTAACACCAGGTAAACTTTTACTTGTGTTGACAGAAGATAAACCTGACTTTTAGGCAACGATGAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32405
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 |
---|---|---|---|---|---|
ENSDART00000087250 | Essential Splice Site | 1468 | 2349 | 28 | 31 |
ENSDART00000148002 | Essential Splice Site | 1431 | 2312 | 28 | 31 |
Genomic Location (Zv9):
Chromosome 22 (position 27408177)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 26923622 |
GRCz11 | 22 | 26786074 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGAAGAAAGGAAAAAAGAAGAAAACACGGCAGCTTGTGAAACTCCGGAG[G/A]TGAATGAGAGAGGCCTTTTTGACATTTTCGGATACTTGATTTTGATAACC
Long Flanking Sequence:
TGCATGACTACAAGGTATTCCTTATGATCTTTAAAGAAATGAAACATTAAATGATTTGGGAATTAAATGATTTGGGCAACACGGTGCCTCAGTGGTTAGCACTGTTGCCTTCGCGTGGGTTTCTTCCGGTTGCTCCGGTTTCCCCCACTGTCCAAAGACAGGTTTCCTAGTACTGGGTTACAGCTGGAAGGGCATTCAACGCTTAAAACATATGCTGGATAAGTTGGTGGTTCATTCCGCTGCTGACCCTTGATGAATAAAAAGACTAAGCCGTAAGAAATGGAATGAATGCATTAAATGATTCATTAATGCAATGCTTTTGTGTTTGATAGGACATTTTCAAACAAGCCACAGAGGACCGTTTGACGAGTGCAAACGAGCTTCCATATTTTGAGGGGGATTTTTGGCCCAATGTATTGGAAGAGAGCATCAAGGAGTTAGAGCAAGAGGAAGAAGAAAGGAAAAAAGAAGAAAACACGGCAGCTTGTGAAACTCCGGAG[G/A]TGAATGAGAGAGGCCTTTTTGACATTTTCGGATACTTGATTTTGATAACCTCAAAATGTATTTACATCTCTTTCATAAACTCCAAACGTCCTTTATAGACCCCTTTCATCCTTTCTAACAGGGCACACCAGGAGACAGTAAAAATGCAAAGAAGAAGAACAACAAGAAAACGAATAAGAATAAAAGCAGCTTGAGCCGAGCTAATAAAAAGAAACCTGGGATGCCGAATGTAGCCAATGACCTTTCTCAGAAGCTCTACGCCACCATGGAGAAACACAAAGAGGTCTGCTATATCTTCATCAGTCCCTTAACCTGCTTTGAGGCATTGCATGAGTCACATGCATGGTTTAATTTTTAGTTCTTCATTGCTTTCTATGTGAGCATGTTATCTAATTATATTATGACTTTCTTTTACCTGTTCTCTCAGGTGTTTTTTGTAATTCATCTGCATTCTGGGCCCATAGTCAACTCCTTATTACCCATCCTTGACTCTGATCCCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14981
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000087250 | Nonsense | 1931 | 2349 | 31 | 31 |
ENSDART00000148002 | Nonsense | 1894 | 2312 | 31 | 31 |
Genomic Location (Zv9):
Chromosome 22 (position 27410474)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 26925919 |
GRCz11 | 22 | 26788371 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCTTRTTGGGCCACGYGGRCAGCAGGTCATGCAGCMCATGCCGCAAGGA[C/T]AGTGGCCTGGAGGCGCTCAGCCTAGTATGCCAGCAGCYCAGCAGCAGGTC
Long Flanking Sequence:
TGCAGGGTCGAGCCATGCCTCAAAGCCTACCGTCACCACCCGCATCCACAGCCCCCAGCACACCCACCTCGCATCAGCAACCCAACACGCCTCAAACGCCGCAACCGCTGCCCAATCAGCCGACTACGCCAAACGCTGTCGTAATGTCACCAACCTATCCCAATACCCCACGCAATGGACAACCCCTTCCTCAAGCCTCACAGGGCAAACCCGGCCCACAGGCGTCCCCACTACATCAGCAGCAGTCTCCACTCCCACAGCCACCCCAGCAGCAGCCTCCGCCGCAACAACCTCCGCAGCAGCAGCAGCAGCCTCCACCTATGGCAGTCAAGATGGCACGGCACATAGAGATGGTGGCGCAGGCTCAACAGAACTATCGCATGACCATGAATGGCCTTCCCATGAACCACCAGCAGCCGCGCATGCCAGGTGCAATGCAACCACCCATGCAGCTTGTTGGGCCACGCGGGCAGCAGGTCATGCAGCCCATGCCGCAAGGA[C/T]AGTGGCCTGGAGGCGCTCAGCCTAGTATGCCAGCAGCTCAGCAGCAGGTCGCTCAACAGACCCCACAGGGCCCTCAGTCGACCTTGCCTATACAGAGACCCGCAATGCCCCAGCAAGTTGCCCAGCCACGCATGATGGTGCCCACGCAGGGCCCTCGACCGCAAGCACCCCAGAGAGCCGCAGGCATCGCTCCTAATGCCTTACAGGATCTGCTACGCACCCTCAAGTCACCCAGCTCACCCCAACAACAGCAGCAAGTGTTGAACATCCTCAAATCGAACCCGCAACTCATGGCAGCCTTCATCAAACAGAGAACTGCAAAGTACCACGCCAGCCAGCCCCAGCAGCAGCAGCCACAGCAGGGCATACACGCAGCGCAGCCAGCCATGCAGAACATGGCAGCTATGCAGGCTGTGCCACGACCTGGCATGGCCCCTCAGCAGCAACAACAGCAGCCCACACCACAAGGCATGGCAGCTCTTGGTCCACAGGGTCAACTC
Associated Phenotype:
Not determined