ZMP
A5PLH8_DANRE
Ensembl ID:
Description:
LOC100002625 protein [Source:UniProtKB/TrEMBL;Acc:A5PLH8]
Human Orthologue:
AKAP6
Human Description:
A kinase (PRKA) anchor protein 6 [Source:HGNC Symbol;Acc:376]
Mouse Orthologue:
Akap6
Mouse Description:
A kinase (PRKA) anchor protein 6 Gene [Source:MGI Symbol;Acc:MGI:3050566]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa42872 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa36327 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa13083 | Nonsense | Available for shipment | Available now |
sa36328 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa42872
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 |
---|---|---|---|---|---|
ENSDART00000105333 | Essential Splice Site | 112 | 2142 | 1 | 14 |
ENSDART00000109573 | Essential Splice Site | 112 | 304 | 2 | 4 |
Genomic Location (Zv9):
Chromosome 17 (position 8863690)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 8861032 |
GRCz11 | 17 | 9018212 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCAGGACAGCAGCAATAGACATGTGGATGTGCATCTGGTGCAACTCAAG[G/A]TAAGAATGCTTTAATACTCAATCCTGATTGGTCAGTTGTAGCATTGAGGT
Long Flanking Sequence:
ATTGATTGTGTGGAACCAAGCATTTTTTTTACAGTGTGTGTATTGTTTCTTAAACTAAAGTGTTACCCTTGTTTGTTTTTTAATCCCATTCTCATTTTTTTGTTTCTTTTTTCTAAACAGATAAACCAAAAGTCCCCATCCTCAGGATCCTATTACATTTCACCATGAACGTTGTCATATCACCAAATGCCAGTGAGGCTTCGTCCCCTATGATAACTGCAGTGACCCCAACCCTGGAACCGGGCCCTGATAAACATGATGATCCAGACGTGTGTGAACCCAGCGTTAGCGCTGATGGGTCGACCCAGAAACAAGATCCCTACCGCAGGTTCCAGAAACCTCCGCCTCTCCACACTGGGGCCGACTGGAAGGTGGTTCTCCATCTGCCGGAGATCGAGACCTGGCTGAGGACCACCACGGAGAGGGTCCGAGATCTCACACACTCTGTGCAGCAGGACAGCAGCAATAGACATGTGGATGTGCATCTGGTGCAACTCAAG[G/A]TAAGAATGCTTTAATACTCAATCCTGATTGGTCAGTTGTAGCATTGAGGTCTGAGATATTTTTGTGATGCTGTATTTAGGTTTGTTCACGGAAACACACCAGTGCTATAAGTGTTGTTCAAAAGTTTAGTGTTGAAATAAAAATTGAATTAAGTGAAGTTTATTCATAAACTATTTTAGAGATGATCACATACTTATGATTGATCACAGCTGGTCCCGCATTATTCAATTCATGATTCACCAATCAGACGATTCCTAAGGCTCTATAAATACCCTAAGTTTCATATAACAGCCATCTTTGTTTTGAAGAATCCCCCTTCCACTTCTACTCCTCCTCCTTTCCTAGATGGGTGACATGGTGACTCAGTGGTTAACACTGTTGCCTCACAGCATGAACGTCACTGGATCTAATCCTTACCAAGCCAGCCGACATTTCCGCGCAGAGTTTACATGTTCTCCATATGCTCACGTGGGTTCCCCGGTTTCCTACCACCATCCAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36327
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 |
---|---|---|---|---|---|
ENSDART00000105333 | Nonsense | 801 | 2142 | 7 | 14 |
ENSDART00000109573 | None | None | 304 | None | 4 |
Genomic Location (Zv9):
Chromosome 17 (position 8988709)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 8986051 |
GRCz11 | 17 | 9143231 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTCTGGGTTTGTTTTTTGGCGTCAGCAGGTGGAGGTCCAGCAGAGCCAT[C/T]GAGAGGCCCAGAAGGACATTCTGGATCAGATGAGAGGGAAACTTCAGAGT
Long Flanking Sequence:
CGTCTGACCTTTCTGGAGGCATCTGCCGAGCAGGCGGCGGGCGAGAACGCTCTTCATAAAGTGTTGAGAAATGAGCAAAAAATCAAAGCCGTCTGTTGGAGCTTTTTATTGGCTCGCTCATTCATCGGCTCGCATTTTGCACAATAACTGATCTCCGTCAAGCCAATGTAGCCAATTTTCTCAAGCACCGAGGAGAGATACATATTTTTTTCCATCTGATTTGAAAAAAAGCTTGTACAAGTGCTTCCTAATCGCTACTGAAAACCGACGCTCACCGCTGCTCGCTCCACGCCAGTTTTTATTGTTGCCATATTGATTTGGCTAAATGCTACGAGTCTGAATTGGTTTAATAGTTTCGCAAGTTTATTATGTTTTAATAGTTCTTGAAGTTGAATCAATGGCGTAGTGGTAATTGTTTTCCAAGGGGTCGCTGAAATTATAACGATTCCTTCTCTGGGTTTGTTTTTTGGCGTCAGCAGGTGGAGGTCCAGCAGAGCCAT[C/T]GAGAGGCCCAGAAGGACATTCTGGATCAGATGAGAGGGAAACTTCAGAGTCAACAGTTGTGGTCCGGCAGCAGAGGTGTCGACTTCAGTCTGATGTCCAGGACTAGCAGGTATGATTTAAAATGTGTTTAATCGATACCTTGTGAGAGCTGAAAACTCATTTAGGTTTTTATGCTAAACCTCACGTGTAGTTAAGGGCAAAATTGTTCGACCTCCTGTGAAATTTTCATTCTGTTTCAAATATTTTCCAAGCGCTGTTTAGCAGAGTTCACAGTATTTCCTTCACTAAAAAAAATGACATTTGCAGTTTATTTAAATTGAACAACATATTAAGTTCAATCTACTTCAATTTTTAAAAACTAAGTTTATTTAATTCCTTTATGTTATCCCAACACAAATTGTAAAACCCAGTATTTTTTACAGTGTATCTATATATTTTTTTTCTTACTATTTGGCTGGAATATTTAAAAATATATATTATAGGTATATATTATTAGCTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13083
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 |
---|---|---|---|---|---|
ENSDART00000105333 | Nonsense | 1186 | 2142 | 12 | 14 |
ENSDART00000109573 | None | None | 304 | None | 4 |
Genomic Location (Zv9):
Chromosome 17 (position 9099034)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 9096376 |
GRCz11 | 17 | 9253556 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AACTCTATCAACAACCCCAATATAATCACAAATCATCTCCAGCCAAAGCG[C/T]AGCAATCACTGCTCARGAGAGTRAGCATGGATTCATCCTTCTCCTCGGCY
Long Flanking Sequence:
ATAAAGAGGATCATATAAATAGACTCTTCCCGCTTAAACAAGATGCAAAGCAATTTGTGTCATCATGCACTGCACTGAATGCCCATATCTATGCAAAAACGTGTTTGTCATAAATTAACTTGGCATTTGATCTAATTAAAAGTGCAATCAAGAATTTATATGCCTTGTCATCTTCTTTTTTCTCTCTCTCTCTGCTGCAGGTCCCTGGGAACCTCATTGAGCCTTCGCTCATGGACCTCCATGGCCTGACAGAAGACTCTTGGGAGTGGGACGAGATGGACATGACCATCAATATGGAGACGCAGAACTGTGAAGATGAGGAAACTCCTGGATCTAAATCACACCTTAATTCCCCAAAGGAGCCTTCGAGTCTCACTGAGTCATGCCCAACTGACACACAGTGCGCTCCATCTTCCCATGTTTATCAGGTGTACAGTCTGCATAACGTAGAACTCTATCAACAACCCCAATATAATCACAAATCATCTCCAGCCAAAGCG[C/T]AGCAATCACTGCTCAAGAGAGTGAGCATGGATTCATCCTTCTCCTCGGCTGAATCTCTACCTGATATCCTGGGAGACCTGCTGAGAGGGAAACAGAGGCTGCTATCAGATTCAGCCAGGAGATCAGAAAGCGAAAGTGGGATAGTAAGTGAAGGGGACACAGAGACCTTGGGTAACTCTGAAATTTGCCTGCTGTGCCAGAGCGATGATTTAAAAGTTTGCGTTACCCTCACTCCTCCTATCAGAGAAGATTCACATAATAGAGACAGAGTCTCAGATGAGGACATAGACAGAGTTTTGGAGCGTGCCAACAAGTGCGCTGAATATGGTGACAGTCTTACCATTGTGAAGAGAGACCAGCGATGCCATGGCACGAGAAAGAAGAGAGATGATTGTGGAGAAAGCAGAAAGAAACATCGCAAGGAGCCTGTGAAGATCCTTGCCAAAGGCCTCGGGCTATGCCAAGAGTCTGGCGATGAAAATCCCAGCATGAGTGGAGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36328
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000105333 | Nonsense | 1401 | 2142 | 12 | 14 |
ENSDART00000109573 | None | None | 304 | None | 4 |
Genomic Location (Zv9):
Chromosome 17 (position 9099681)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 9097023 |
GRCz11 | 17 | 9254203 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCCCAACAAGCAAAGAGACACTCACTCGTAGCACTTCCCTAGAAAGTTG[G/A]CTTGCTCCGTGTAAGAGTGCAGAGGACGGGGGAAGTAAGGAAAGTCTGAG
Long Flanking Sequence:
AGTGAAGGGGACACAGAGACCTTGGGTAACTCTGAAATTTGCCTGCTGTGCCAGAGCGATGATTTAAAAGTTTGCGTTACCCTCACTCCTCCTATCAGAGAAGATTCACATAATAGAGACAGAGTCTCAGATGAGGACATAGACAGAGTTTTGGAGCGTGCCAACAAGTGCGCTGAATATGGTGACAGTCTTACCATTGTGAAGAGAGACCAGCGATGCCATGGCACGAGAAAGAAGAGAGATGATTGTGGAGAAAGCAGAAAGAAACATCGCAAGGAGCCTGTGAAGATCCTTGCCAAAGGCCTCGGGCTATGCCAAGAGTCTGGCGATGAAAATCCCAGCATGAGTGGAGATGATGAGAGAGTGACTACACACCGAAAGCTCCAAAAGGAGTTTGCACAGCTCTCCCAGGGGTCTTCCCTAGACTCCCTTTATGCAGTGGGAGAACTGTTCCCAACAAGCAAAGAGACACTCACTCGTAGCACTTCCCTAGAAAGTTG[G/A]CTTGCTCCGTGTAAGAGTGCAGAGGACGGGGGAAGTAAGGAAAGTCTGAGGGACATCGGATCGACTGTGGAGCCCACTGGGGAACTCAGCAGAAGAACTCTAGAGCTTCTGAAACGCCTTGAGAACATCCAAAGCCCACTCGCTCTGAAGATGACGCGCAGTGTGTCTGACGTAACGCTCCAGAGCAGCTCACTGTGGCGTGGGTCACGCTCGGCTGGCGCTCCCTCCTCCATTAACGAGAGCTCGGCAGCCTCCCTGACAGAGCTGAGCAGCACTGAAGACTCCTCGGTGGCATCCGAAGACTTAGCCGTGCAAATGAACCGCTGCATAGCTGCTGAATCCAATGCTTCCTTCCGAAAACATTGCCACAGCCAGCAACAAGCGGATGAGACAGATGCTAGTATCAGTATGGTTGTTAACATTTCATGCACATCAGCCTGCACCGACGATGAAGAAGACAGCGATCTTCTCTCCAGCTCCACTTTGACTCTCACCGAAGA
Associated Phenotype:
Not determined