ZMP
si:dkey-24n17.4
Ensembl ID:
ZFIN ID:
Human Orthologue:
AEBP1
Human Description:
AE binding protein 1 [Source:HGNC Symbol;Acc:303]
Mouse Orthologue:
Aebp1
Mouse Description:
AE binding protein 1 Gene [Source:MGI Symbol;Acc:MGI:1197012]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa16060 | Essential Splice Site | Available for shipment | Available now |
sa6154 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa38770 | Essential Splice Site, Missense | Mutation detected in F1 DNA | Not yet available |
sa34810 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa16060
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 |
---|---|---|---|---|---|
ENSDART00000126440 | Essential Splice Site | 206 | 1022 | 4 | 20 |
ENSDART00000131435 | Essential Splice Site | 206 | 1020 | 4 | 20 |
Genomic Location (Zv9):
Chromosome 10 (position 2841159)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 2786796 |
GRCz11 | 10 | 2813967 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AACACCTCCATCAGTCAAAGAGCATRTGCCGGATAACTGGGACAGCCGAC[G/A]TATGTTTAAAGCAGCATCCATTACTCTSTYTTAAAGGAACACTTCACTTT
Long Flanking Sequence:
TGCTTAAATTGCTTCGTTTACTCAAATAGAGTAAGATCACAGGACTCATTAGGATTCTTTTTTTTTAACTCAAATGGTTTGTTGCAATCGGTTTCCTTAAATGGTTTGAGTTACCTTAACTTTTTGGGTTTTACAGTGTAACAAATGAATAATTTTGGTCCAAGTACATATTGGTTAAGGCCACCCAGTATAAAGTGGGACAAACATTTTTTTTATTTTAATTTAAATGGGTTTGTCCATATATGATAAACACAAGACTAACACAAGAGTGGAAACAATTATGAAAGATTAAGGAAGAATCAACAATTCAATCCCTGATTTTCTGCAACTTGGGACAAAAAAAGTGCATATTATGCAAATCAAGCGGCTGTTTTCTATTAAAATATTGCTAATCACAATATTTATTTTTATTTACTTTCCAACAGACATGCACAGCAAGAAAGACCCCACAACACCTCCATCAGTCAAAGAGCATATGCCGGATAACTGGGACAGCCGAC[G/A]TATGTTTAAAGCAGCATCCATTACTCTGTCTTAAAGGAACACTTCACTTTTTTGAAAATAGTCTGATTTAAAAATTCCCCCAGAGTTGAACAGTTCGGTTTTACCATTTTTTAATCCATTCAGGCAATCTCCTTGCCTGGCAGGAGCACTTTTAGCTTAGCATCATTGAATCCAATTAGACCACTAGCATCTCGCTCAAAAAAGAAAAGAGTTTTGATAATTTTCCTATTTACAGCAGCAGACCCAACGATATTACGCAGCACCTGAAAATAGTCCCCAAACTTTTTTATTTTGAGTGAGATGCTAATGGTCTAATCCGATTTAATGATCTTTGCTAAGCTAAGCTCAAAGTGCTCCCACCAGACCCGGTGATCTCCTGAATGGATTAAAAAATGCACTGTAAAAAACGCCGGGTTCCACACAATTCATTCATGTTGTCCCAATACAAGTTGGTTAAGTTAACTTTTAACAAATTTATGTGGATCAAACATAAAAAAATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6154
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000126440 | Nonsense | 230 | 1022 | 5 | 20 |
ENSDART00000131435 | Nonsense | 230 | 1020 | 5 | 20 |
Genomic Location (Zv9):
Chromosome 10 (position 2842076)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 2787713 |
GRCz11 | 10 | 2814884 |
KASP Assay ID:
554-4769.1 (used for ordering genotyping assays)
KASP Sequence:
CTCATTCCTAAAGTCAAGCAGCCGTCCTCCACCGATGACCCGAGTATATA[C/A]TTACCAATCCCAGGTAATCAAGTACATACGCTRACAYTTCTWACCAAAAC
Long Flanking Sequence:
CCACACAATTCATTCATGTTGTCCCAATACAAGTTGGTTAAGTTAACTTTTAACAAATTTATGTGGATCAAACATAAAAAAATTAAGTTGTCCCAAGGAATATGGATAGTTGAATGGATAGTTCAGCTAAAAATGTCAACACTGCCACCATTTACTCATCCACTTCTGTTCACTGGATGCCAATGGCAGCTGGTTTCCAACAGTTTTCAGAACATCTTGTTTTGTGTTCAAAAAAAAAAAAAAAAAAATCATGAATGTTTAGAACCATTTGAGTTTGAGTAAATAACGAGGACGTTTTCATTTTTAGGTGAACTATCCCTCATATTGGAAATTGGTTCTTTAGATTTTAGATAATTTTATTAGGTTAACCCTAACAGATAATCAGATTCTACTAATACTGCTACTAATAATACATTTTATCACCTGACAGATGAAATCCAAGAGCCTGACCTCATTCCTAAAGTCAAGCAGCCGTCCTCCACCGATGACCCGAGTATATA[C/A]TTACCAATCCCAGGTAATCAAGTACATACGCTGACACTTCTAACCAAAACACACTTGCCCACTGACTTACAATGGTGAAGAATCTCCCATTCAAAAAACCATAGAGGTTTGGGAGTGGGCTCATTTAACTCAAGCAACCAATCGGTCTTTCAGGAATATTCTAAAACTGCACACCTTAGCAACCATTTAGAGCACCCTAGCAACTGATCTCATAGACTGCCATTATATCTTTATGCTGCAATATCATAGACTTTAAGCTGTCAATTGACTTCATAGCAACTAAACAGACTAACCTAGCAACCATTTAACAACAGCAACATCTCTACATCAGAACATCGTAGGGATTTGGATATTGGCTTGTTTCACTTGTGCTAGCAAAACGGGGCTTCCTGATTACTACACATGCTAACAGTAATTAGCAAACTGCTAATAACGATTATTTACATTCTAATAACCAGTGCAATAACATGCAAGAAATGCATAATATATATGAAAGAGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38770
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, Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000126440 | Missense | 384 | 1022 | 10 | 20 |
ENSDART00000131435 | Essential Splice Site | 383 | 1020 | None | 20 |
Genomic Location (Zv9):
Chromosome 10 (position 2849868)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 2795505 |
GRCz11 | 10 | 2822676 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACGAGAGGTGGAGTTTACCGGTGTAATCACACAGGGCAGAAACTCAGAG[T/C]CAAAGTAAGTCAACCATCAAAACACTCACGTCGTTTTATAACAACACACG
Long Flanking Sequence:
GGGCGGGGCTTTCCTCCTCTGTTGACACGTACAAAGAGTGAATGCCAATCAAAGTGTTTCTCCAGGCTGTTTTTTTCAAGTGTGATAATAAAAAATGGAAGTAATTAATTTTTACCATTATGAGGTGGTTATAATCACAGACTGCTGCCACACAACTGTGTTTAAACCCCTTATACAAGCGATCTTTGCATAATAGGTCCCCGTTATGTGTACTAATATGTGTTTATAAAAATAAATGCACATATTTTGGTGCACTTACAGCATTTTGCAAAGTTTTGTTCCTTATTTTAAGGATTTTTAAAAATTATAAGTATGGTTCAACATGGACAGAAACAGGAATCTTAAAGTAAACATCTGTTTTGCAGAATTCGGCTGATGAGGAGGATGTTTACGGTGGAGCGTGGTGCGCTGATACGGAGGAGAAGGAGCACTGGTTTCAGGTGGACGGCCGACGAGAGGTGGAGTTTACCGGTGTAATCACACAGGGCAGAAACTCAGAG[T/C]CAAAGTAAGTCAACCATCAAAACACTCACGTCGTTTTATAACAACACACGATGCAACAAGATAACATCAACAAGCAATTTGTCTCTCTGCACCAAAAGTGACACGACATGACAGAAACATTTAACCACTTAAACTCTGCTGCTATTTGGGGATTTCCGCCTGGATTTTGTCTACCCAAATTTAAAAGCTTCCCAAATCCACATGCAGAGGTGTAAATGCAAAAATGTGGTATCATTTTAAAGAAAACCCTTTGAATTTTCATAAAACACTATTGAAAGTGTTTAAAATAACTGTATATGTCGTCTGTGTTATAATAAACACCTAAAAAGGAGGCGCTTTTTGTATTATTATTTTTTATAAACTCTAATTTGAAAGTGTACCTTTTAGGTTGTGTGTGGTTTAGCGTGCTGTAATTAATGTTGGTGGTTCCTGCACATGTCTGTAATCATAGGAAAAAAGAGAAATGTCTCCACCATAATCTATGCTAAAGTTATTGTATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34810
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000126440 | Nonsense | 659 | 1022 | 17 | 20 |
ENSDART00000131435 | Nonsense | 657 | 1020 | 17 | 20 |
Genomic Location (Zv9):
Chromosome 10 (position 2859256)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 2804893 |
GRCz11 | 10 | 2832064 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAGTGTTTAATTTCTGAAACATATCTGTCCTCAGGTGGCGACTGAAACT[A/T]AAGCCATCATCAGCTGGATGGAGAGGACGCCGTTTGTTTTAGGCGCGAAT
Long Flanking Sequence:
TCAGGGATCTGAGATGGGAAACTGGGCTTTGGGACACTGGACAGAGGAGGGGTACGACATTTTCCAGAATTTCCCAGACCTGAACAGTGTTCTGTGGGGTGCGGAGGACAGAGGATGGGTGCCGCGGATCGTTCCCAATCACCACATTCCCATCCCTGAGAACTTTCTCAATGGCTCTGTGAGTCAAGCTGAAGAGTCCATGTGGACACGTTCATTCTGTCTTCAGGATGTTTTACTGGATCTACATTTTTTGGTTCTGTGTTTGTATGTATTTTCACCTTAAGCAAAGCTGAATTTGCAACAAAATAAAGGCCAAAGTATCAGGAAAATAAACCAAAGCTGATATCTTGGAAATGTCGTAGGCTATTTCCTGTTTAGTAGACATGCATGACTTCTTCATGTATGAACAATTTGCTTGTAGTCACAGAAAATCCTCCATACTTTTATCTATCAGTGTTTAATTTCTGAAACATATCTGTCCTCAGGTGGCGACTGAAACT[A/T]AAGCCATCATCAGCTGGATGGAGAGGACGCCGTTTGTTTTAGGCGCGAATCTGCAGGGCGGAGAGAAGCTGGTGGCGTACCCATTCGACATGCAACGTCCACCGCGGGCCACGAGCACGGACGGACGGGTCGGTCAGCCGGTGCAGGAGTACCACAACATGAACGAGGAGACCTGGGCTCGGATTCAGCGGCAGAACGAAGGCGCTCTCCGCGAAACAGCGGATGAAAACCTGTTCCGGTGGCTCGCCACGACGTATGCACACAGTCACCTCACCTTGACGGAAAACCACCGCGGGTCCTGCCATACCGATGACATCACCGGCGGACAGGGCATCATCAACCGCGCCAGCTGGAAACCAGTTGTGGGCAGTAAGTGATGATAACTGGAAAGAAATTGTGAATCTACTTTGCTATTTCTGTGCAGAATTTTGTAAAATGAAAACGTTTAATTGGACTCAGTGTGAAAGGTTTGTGTACGGGACAAATGTTTTGGAAATGAA
Associated Phenotype:
Not determined