Busch Lab

ZMP

akap8l

Ensembl ID:
ENSDARG00000089073
ZFIN ID:
ZDB-GENE-040426-2303
Description:
A-kinase anchor protein 8-like [Source:RefSeq peptide;Acc:NP_998384]
Human Orthologues:
AKAP8, AKAP8L
Human Descriptions:
A kinase (PRKA) anchor protein 8 [Source:HGNC Symbol;Acc:378]
A kinase (PRKA) anchor protein 8-like [Source:HGNC Symbol;Acc:29857]
Mouse Orthologues:
Akap8, Akap8l
Mouse Descriptions:
A kinase (PRKA) anchor protein 8 Gene [Source:MGI Symbol;Acc:MGI:1928488]
A kinase (PRKA) anchor protein 8-like Gene [Source:MGI Symbol;Acc:MGI:1860606]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa19640 Essential Splice Site Available for shipment Available now
sa24861 Nonsense Mutation detected in F1 DNA Not yet available
sa19641 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa19640
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000126152 Essential Splice Site 7 508 1 11
Genomic Location (Zv9):
Chromosome 1 (position 60320276)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 58530232
GRCz11 1 59237058
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTCACACACACAGATCACTGCAGCACGATGGATAGAGGATATTCTTCAG[G/A]TTTGTCTTTTATTCTTTTTTACCTGTTTTTCAGTCGTATATACGTGTGGA
Long Flanking Sequence:
TATTTATATACCGTTGTTGTGTGTATGCGTTTCAGAAACGTGGGGACCAAATATGTGTATTTTCTAAATAGTTTTTTTTTTATAAATCTCTACGTATACATGTATATGATAATATCCTGCTGTGGTGGTTTGTGAAATTCTCTTTATTCAAGTTAAAATCATTTGTTCTTGCTCTGCGGAAATCTGTCTTGTGTGTGTTTTAAACTCAACTTATTAAAATAGATACTGATATACTGTGTCAGAGCTGTGTTAGTTTGCACGGTTTAACGCAGACAGTCAAACACACACACACACACACACACTTCTGTTTTAGAAGAAAGGACAAAAAATTGTGTTTTTGGCTGTCACCGCTCAGTCATTGGGTCATTCATGTGTCAATCATTTAACCACACCCGTGAGGGCGGAGCTAGAGTGGTCTGATAGAGCCTGAGCGCCGCTCGTTCACATCAGGTTCACACACACAGATCACTGCAGCACGATGGATAGAGGATATTCTTCAG[G/A]TTTGTCTTTTATTCTTTTTTACCTGTTTTTCAGTCGTATATACGTGTGGATGTGTTTGTTTGTATCTTGTAAGTTCTGCATTGACGTGTTGTGCTCAGCCGCCTGGCCTGCAGTCTCATTGCGTGAAATGGCGCAGGCCAAAATATACGTTAAACCAAGCTCAAAACCACTGTTAAACAGGGCATTAGTGAAGAAACTTGCTTTAATGTATGTGTCGTGAGGTGAATGTGAAGCTCGATGTTGTTTATTGTCTTCCGGAAGCGGTGACGGTGATTTAATTAAATGATCAGTCGGTTAACCGTCGTTTTCCCCGTAACGTTACTCGTGTTTGGTTTTCGCTTTTGCCGTGAGTGCACGGTTGTAATTCGCGATCTGTTGTCCGGACCGTGTAAATGCGTCACTGGTTGATGAACGGAACAAGGCCGAGTGGCGGAATCGGTGAACCGTACGCGGGTTTAGCTGTTTTAAAATGGCGGCCGTGTGAATCTGCGGCTCTATTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa24861
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000126152 Nonsense 28 508 3 11
Genomic Location (Zv9):
Chromosome 1 (position 60322117)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 58528391
GRCz11 1 59235217
KASP Assay ID:
554-7466.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACCTGCTGGCTCATCTGTGCTGTGTGCTGTGCTCAGGCTCAGGTGGTTA[T/G]GATATGTACGGCTATAAAGACTCAATGTCAGGCGGTGGTGGGTACGGTGG
Long Flanking Sequence:
CCCAAACAGTGGTACGGCATATTTTGCAAACTTAAGTTTCATCAGATGGTTTGAAAATATCTATTTAGAATGATTGGGATGATTCTGTAGTGGAGTGCATCTGCATAAAATATAATAAACTCATTTAAATAATAGATTAATACAATAAAGCGAAGTTAAATCAAGTGTCTTACTGGTTTTTGAGTCTAACAGTTTTCAGGTACTGAGTAATAAAAATAATCATTATTAAAGTCACTAATGGTTTCTTATGGCTGAATGTTTTTAAAATCCTCACAGTCACACGCCTCAGAAACACATGTAAATAATTGATAATAAGCATGTTATATTGTAAATGCTGTGATATGGCTATTGTGAATGATCACTTTGATGCGCTATATTGTACAGCTCTGACAATGGGAAAGGAGGGAGCGTCCTGAACCGCACCGCTCTGTATATGCACTGACTGTATGTAACCTGCTGGCTCATCTGTGCTGTGTGCTGTGCTCAGGCTCAGGTGGTTA[T/G]GATATGTACGGCTATAAAGACTCAATGTCAGGCGGTGGTGGGTACGGTGGTGGTGGCGGGTACGGCTCCGAGCGGATGAAGAGAGGTATGTCTGGAGGATCCCTGCTGTCCAGCGGCGCCAACGCAGACGCCGTCATCGCCAAAATCAACCAGCGGCTGGACATGCTGACACAGCTGGAGGGAGGGATGAAGAGCGGCTCACGAGGGGACAGGTAACACACACACACACACGCTGGAGACAATAACACACCTGTAACTGCACTAAAACACCTTCAGATGAGCGTCTGACAGATAATTCAGTGCATTTGTTTGTGTTAAGCTTAAGGAACAAACACTAATTATGGCAGATCCACTTGATTTATTTACTTTCAGTTATTGAAGTGTCTGTAGGCACTTGAGATTATGGCCGATTCCAGAACTGCAGCTAGATTTTACACCTTAAAGAGAAATCTAGGGCTGGGCCATTTGGCAAAAAAAAACTTTTTTTTTTTTTTTAATAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa19641
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000126152 Nonsense 126 508 4 11
Genomic Location (Zv9):
Chromosome 1 (position 60324873)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 58525635
GRCz11 1 59232461
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCGCCTCCATGGGCCCTCGAGATCTCTACAGATCTGCTGGCTACGGTTA[C/A]AGCGACTCCCGGGGCGACATGATGGCCCAGCGCGGAGGCTTTGGGCTCAT
Long Flanking Sequence:
CCTGTTTAAAGCTGATCATCAGTCATAGTCTTACTGCATTTCTGATGCCATAAATGCAGAGCAGCCCATTCACACACAGCCATGTTGATCATCGAAGCCTGCACGGGCATCAGCAGTCCAGATGTGGTGACGGTACAGACTCACACACACACACTCCTGTCCTCGGCTTGCCCTGATCTGCACAGACACATCTGCCTCTCCAGATGCCCTCACTGAAGATCTCCTGTTTCCAGATCAGTCCGTTGCCTTACGCCAGCATCTGTGCAACTGTGTTCTGAAGCTTTTCCACAGCCTGGAGGCAGCAGTAGCTGTGGAAGGGCTTGATGAACGAGCGCTAATGATGAGTTTGTGTGTGCGTTGTGCTCTGCAGCCGCACTCAGTGACCTGTGACCTCTGCTCTGCGCCTCCTCCTTCTGCAGGTTTGACCAATACGAGTCTTTCGACTCGCGCTCCGCCTCCATGGGCCCTCGAGATCTCTACAGATCTGCTGGCTACGGTTA[C/A]AGCGACTCCCGGGGCGACATGATGGCCCAGCGCGGAGGCTTTGGGCTCATGGGTGGAGCCGGAGGGGGCGGAGCCTTTGATGGCTTTGGATCTGGCAAAATGAGGCCGACTCGAGACTCCTTCTCGGGCTCTGGCTGGGGGGCGGGGCAGAGATCCCCACGCAGGGGTGGATCAGCCGGGGGGCGTGGCTTTGGCCGCAGGCAAGACTCCTCTGGGGGAGGAGGTGGGCGTGGCGGAGGCCATGGCCACTCCCCTGGTGGCCGAGGAAAGCTGCCCTCGCTGCTGGGCCAACGCATGTACCCTGACAGCGGGGCCTTCCAGCCCCAGCGCGGGCCCCAGGACTTCCCCGTGCGGAACTTCGGAGGGGGCCCGAGGGCCAACCGGCAGCGTGGCCGCAAGAGACCTCTGAACCGAGTAAGTACCGCCCACTGCCTGTGGGGGGCGTGGCTGAGAGATCAGCGCTCACCCCTGCACGTAGAGGCCAGTCCAGCCCAGAACAG
Associated Phenotype:
Not determined