ZMP
hdac8
Ensembl ID:
ZFIN ID:
Description:
Histone deacetylase 8 [Source:UniProtKB/Swiss-Prot;Acc:Q7SXM0]
Human Orthologue:
PHKA1
Human Description:
phosphorylase kinase, alpha 1 (muscle) [Source:HGNC Symbol;Acc:8925]
Mouse Orthologue:
Phka1
Mouse Description:
phosphorylase kinase alpha 1 Gene [Source:MGI Symbol;Acc:MGI:97576]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa14948 | Nonsense | Available for shipment | Available now |
sa31597 | Nonsense | Available for shipment | Available now |
sa10754 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa14948
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 |
---|---|---|---|---|---|
ENSDART00000009184 | Nonsense | 155 | 378 | 5 | 11 |
ENSDART00000083190 | Nonsense | 1153 | 1376 | 33 | 39 |
ENSDART00000108984 | Nonsense | 155 | 378 | 5 | 12 |
ENSDART00000136047 | Nonsense | 56 | 279 | 2 | 8 |
The following transcripts of ENSDARG00000003021 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 53160613)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 51430363 |
GRCz11 | 7 | 51705433 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAATTGAATGTGTGTTGTTATATAAGGGACGAGGCATCTGGCTTCTGTTA[T/A]GTGAATGACGCGGTTCTTGGAATCCTCAAACTTCGGGAGAAGTATGACAG
Long Flanking Sequence:
CAAACCCCCCTCTCGATGCTCTCTTTTGTTCAGGTTATGACTGTCCGGTGGTGGAGGGTATTTTTGATTACGCGGCTGCCGTTGGAGGAGCCACTCTGACTGCTGCCCAGAATCTGCTGGATGGAAAGTGTGATGTGGCTATCAACTGGGCCGGAGGGTGGCATCACGCCAAGAAGTAATACAGCACAGCGGGCCTTTGTGCCCACCCTCTTGTGTTTCACCTCTACATCAATCATTGAGATGCCAGTCTCATGCCAGTCTCATCTTTAGCATATAAGGAGATCTGTGAGGTTTACTATTTCGATGTTTTCGTAACATGTCAATGTTATGGTTTGTTTGCATGAGACTGCTAAACAAGCCTAGTGTTGGGTTTTTGTAAAATATGTTTGTTTACTGTAGATTATTGTTTACGTGTGTGCATGACACTGTTTAGTGGGTCACTGGAGCAGCTAATTGAATGTGTGTTGTTATATAAGGGACGAGGCATCTGGCTTCTGTTA[T/A]GTGAATGACGCGGTTCTTGGAATCCTCAAACTTCGGGAGAAGTATGACAGAGTTCTCTATGTGGATGTGGACCTTCACCATGGAGATGGTAATAACACTTCCACAACAATAACCATAACAAGCTGTTGTTGTTAATTTCATTTAGCATGTATTTAGTACATAAATTAGCCTAAGTTTTAAATCGGACTTTCAAATTCATCTATATTTACGGCAAGAGAGAATATTAGGTGATCATGTCACTCTACTAAATCTTTTTAATGATTGAAATGAAGATATTTATAAATATATTTATATAAAATATGGTAACACTTTACAATAAGATTCTATTAGTTATTAGGTAAAGATGCAGTATGTAAGTTTGACACCTAGTGGTATTGCACACCTGGTTCAAAACACACTAGCGCAGGTTGCCAGATTGATGTCCTAACCAACACCTTAAATTTTTATTTTAGACATTGCTTCTATTTCTCACAGGTGAACAACACAAAACTGACTTTGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31597
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 |
---|---|---|---|---|---|
ENSDART00000009184 | Nonsense | 297 | 378 | 8 | 11 |
ENSDART00000083190 | Nonsense | 1295 | 1376 | 36 | 39 |
ENSDART00000108984 | Nonsense | 297 | 378 | 8 | 12 |
ENSDART00000136047 | Nonsense | 198 | 279 | 5 | 8 |
The following transcripts of ENSDARG00000003021 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 53153442)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 51423192 |
GRCz11 | 7 | 51698262 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACTTCTGTTGGAGTCGCAAAGTGTCTAACCTATATACTTGGCTGGGAGT[T/A]ACCTACTTTGCTACTAGGAGGAGGTGCGTGTTATTGCTTTTGTTAAATTG
Long Flanking Sequence:
CAATTTAAAAATGACAAACCTTCAAGAACTTGACTAATCATGGTGAGGTAACTTTTACTTTTAGGTTTACAATCCCTGTACTGTCCTTATAAATATGGATGTTCTTGACGGAGGACATTAACATTTGTTTCTCAGGCACAGGTGATGTGACTGACACTGGGCTGGGTAAAGGACGCTGGTACGCTGTTAACGTCCCCTTTGAAGATGGCGTCCGTGATGATCGGTACTGCCAGACATTCACTAGGTTTGTAAAGATCCAATAACTAGTCAATCCACTTAATTCCTTCTAATGTTTGTGGTTCAGTGTCATTTTAATACTTACTTTATTACTTTTTTCTGTTTTTCTGTCAGTGTGATGCAGGAAGTCAAAGCTCTGTTTAACCCTGAAGCAGTTGTGATGCAACTGGGTGCAGACACCATGGCTGGTGACCCTATGTGCTCCTTTAATATGACTTCTGTTGGAGTCGCAAAGTGTCTAACCTATATACTTGGCTGGGAGT[T/A]ACCTACTTTGCTACTAGGAGGAGGTGCGTGTTATTGCTTTTGTTAAATTGTTTTCTCATTAAATAGGATAGTTCAATCAAAAAAAAATTGTCATCTTTTATCACTACATTTCCACAAGACTGTTGTTTATCTCTCAATACAAATGAAGATATTTTTTAAAGTCTTGACTTTACTTTAAAGTGTCCTTGTTACTGTGCAACTTTTCATTTAAATACTGACTAATATTAATTAATTACATGTACTTACTATATGGTTGGGGTTTGAAAGCAGAGTTAGGTTCAGAGTTTGTTGTGTGCCATTATACATTACTAAAGTAATTACATTTAATAAGTACATGGAACATGTTATGTTTTAAAAAAATTCTTTAGATATGAAAAGTAATTTACATGACATAATTTATAAATTCCTCCTCACCACACTCGCTCATCTATATCTATATGTTTCTTGCCTTGTACAATGTTGTGCAGTCATGTTAAAATATGAAGGAGCTATTCCCAAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10754
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 |
---|---|---|---|---|---|
ENSDART00000009184 | Nonsense | 307 | 378 | 9 | 11 |
ENSDART00000083190 | Nonsense | 1305 | 1376 | 37 | 39 |
ENSDART00000108984 | Nonsense | 307 | 378 | 9 | 12 |
ENSDART00000136047 | Nonsense | 208 | 279 | 6 | 8 |
The following transcripts of ENSDARG00000003021 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 53148730)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 51418480 |
GRCz11 | 7 | 51693550 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCACTCACTGTATATACAAATCTGCCTCTCTCTCCTTTCTCAGGCGGCTA[T/A]AACCTTGCCAATACTGCCCGCTGCTGGACCTATCTAACGGGGACCGTCCT
Long Flanking Sequence:
GCCTAAACCCAATGATTTGGAGGAGTGTTCCAAAACTTTTGAAAACATATTCTATTAATAACAAGTTCTTATGTTTTAAACAAGTGGGTTGTTGGTTTGTGTGAATCACACTTAAAGACAGAGCTTAAATTTTTAGATGTATTGTCCATTTATCAGCATTAATCAACAGGCAGTTTCAGCAGTATTGCCTCAGCTTGTTTCCCCTCCACGTATTTACGCTGAAAACTCCATCTTCTGTCCTTATTGCCAGCTTTCTGACTCGGCCAAAAAGTTTATCAGTGTGTTGTTACGGCCAGGGGGGGTTGGGCTAAGAGAAGAAAGTGAACTTTTGTGATTTTGAAATGAGCTCTAAGCTGCAGACCTGCCTAGCCAAGCTCTAGATGAAAGGTAGTAATTACACTAGTACAATGAAGCCCTTTTGCTGACTTCAATCCCCCATCTCTCTCTTTTTCACTCACTGTATATACAAATCTGCCTCTCTCTCCTTTCTCAGGCGGCTA[T/A]AACCTTGCCAATACTGCCCGCTGCTGGACCTATCTAACGGGGACCGTCCTGGGACAGACTCTGTCTTCTGAGATCCCAGACCATGAGGTGAGACCCTGTTCCCTCTCTTCTTTCAGCAGCTGTCTAAAACCCCGCTCTCTCCTCCTCTTCCTCTTCCATTCCTGCTGAGTCACTCGGTCTAATCAAAGATGTCCAAGCACCTCTCAATAACTGGGTTTGTTTTCATGTGATTCAGGAGAAGGGAGGGGAGGCGGGGGGTGTTCGTGTGCACACCAGTGAAGGGGTCTTAACAATACTACTCTGTCCCTACCGGTTGACTGAGAGGGACTTGTGCTTTTCTTTCCTCAACTGTTTATGCCCCCTCTCTTTCTCTTTCCTGAGAGAAAGAGAATGTGTGTGCCCAGTTCTGAGCGAGCTCTTTTAAGAGCTTTTTCATGCTTTTTTTTGAGAAGCTTCTGAGGAGAGATGAAGGGATGGAAAGGCCTTCTGGTTGGTCTAAG
Associated Phenotype:
Not determined