ZMP
zdhhc8b
Ensembl ID:
ZFIN ID:
Description:
probable palmitoyltransferase ZDHHC8 [Source:RefSeq peptide;Acc:NP_840089]
Human Orthologue:
ZDHHC8
Human Description:
zinc finger, DHHC-type containing 8 [Source:HGNC Symbol;Acc:18474]
Mouse Orthologue:
Zdhhc8
Mouse Description:
zinc finger, DHHC domain containing 8 Gene [Source:MGI Symbol;Acc:MGI:1338012]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa25292 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa33559 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa2242 | Nonsense | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa25292
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 > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000014252 | Essential Splice Site | 333 | 751 | 8 | 11 |
| ENSDART00000129878 | Essential Splice Site | 333 | 751 | 8 | 11 |
Genomic Location (Zv9):
Chromosome 5 (position 19816611)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 17387654 |
| GRCz11 | 5 | 17891650 |
KASP Assay ID:
554-7409.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAGCCGATCGCTACAACCAGATCAAGAGTCAGCTGACCTCCAGTGAAGG[T/A]AAGTAGCACTATAAATCAACCGGTCACACTATGATAGTTCACCAAAAAAT
Long Flanking Sequence:
TCGACTGCGCTCAGCCTTCATACTAACATGATGAAAAGTTTTAAATACTCCAGCTCATCCATAAACATGATTTTCTGCTGGAGTCCCATAGGATGTAATGAAGACCACAACTCCCATGATTCCCCACTTAGTCTTGTAGTCATCAATATAAGCCTTTGATTGTTGTAAATATGCACCCTCTAGTGGTATAAATTACAGTGGGCCTTTAATTCCTTAAAATTTGCCTTTAATCCTTTAAAATCACATAGTGTGCACATTCAATCGACAGCCCTAATCGAAATACACAGTATCTCTATTTTTTTTATAGGAACAGTTATAAAAAGTGTTGTGTCTGTAATTAATTCATGCATCCCAGAATCAGTCTTTTTTTTTAATCTTGTGCTTTAGTCCAAGACCAGTCTGAATGGCATGGATGATAAAAGCATTGATGCACAGCCACCTCTGCCACCCAAAGCCGATCGCTACAACCAGATCAAGAGTCAGCTGACCTCCAGTGAAGG[T/A]AAGTAGCACTATAAATCAACCGGTCACACTATGATAGTTCACCAAAAAATGTACTCACCTGTAAGTTGTTCTCATGCTTTATGCGTTTCTTTATTCTATTGAACAGAATAGGAGATATTTTGAAGAAATTTGAAAACCTGTAACCATTCAGGGCTCGCAAAATCTGGTAGCATGACATCCCGGGGCTATTGTTTTTTCAGTCGGGCTACCAAAATCTCCACCTGCCCGGTGGGCTATCACAGTGGAAGAAAAAATATACTTCAACACCTTTACATTCTCTTAAAAAGTGGATAAATATGTATGTGCTGTGCTGCTGATACGGCAGCTATAAATCCACTTGATAATAACCAATATAAAAAGCCAAACTATAAACAACTACCTCTGAAATAACATAACGTGGTGTTTCTATCAGTTTAATCACAAAAAAAAGATAAGTAAACATTGTTTCAGATTATTTAAAAAAATATATAAAAGCCTAAGATAAATAATAAATCTTTGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33559
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 |
|---|---|---|---|---|---|
| ENSDART00000014252 | Nonsense | 415 | 751 | 10 | 11 |
| ENSDART00000129878 | Nonsense | 415 | 751 | 10 | 11 |
Genomic Location (Zv9):
Chromosome 5 (position 19822252)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 17382013 |
| GRCz11 | 5 | 17886009 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCGACTATCGGAGTGCTCCTCTCCACCGAACATACCAGTCGTCCCCTTTC[C/T]AGCTGGACTCCTTTAGCACCACGTCCCGCTCCTTTAGCCTCAAACAGGGA
Long Flanking Sequence:
ATACACATACACGATGTACAATTTAGCTTACCCAATTCACCTATAGCACATGTCTTTGGACTTGAGGGGGAAACCTGAGCACCTGGAGGAAACCCACGCAAATATGGGGAGAACATGCAAACTCCACACAGAAATACCAACTGACCCAGTCGGGGCTCGAACCAGTGACCTTATTGCTGTGAGGCGATTGTGCTACCCACTGCGCCACCGTGCAGCCATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAGTTTCATTTTTAAATTGTTTGATTTTTTTTTCTCAAACATTTCCTCTTTCCCTAGATTGTAATGTGCGAGAACGGTAACCCCTCTGCAGTTCTGGAAGAGAGATCTCACGACTACCGTTCGGAGCCCAATCTAGATCTCCCCGACTATCGGAGTGCTCCTCTCCACCGAACATACCAGTCGTCCCCTTTC[C/T]AGCTGGACTCCTTTAGCACCACGTCCCGCTCCTTTAGCCTCAAACAGGGAGTAAACCGAGCTGACTGCACACCACTAGGTGGCACCAAGCATGAAACCATCACATCCACCCCTCACAGAGGCGTCTTCTCTCCTGGGACGTTATCCGGCCGCAACAGCAGCCTCTCCTACGATAGCTTGCTAACCCCCAGCGTAGCGCCATCTATAGGCGAATGCGCTGCTCATCCGGGCGTCCCATCAATGGGGTTTCACTCACCATATTTACCCACTAAAATGTGCCATGTTCGTGGACCCGAACTTCAACGCCATGCTGGTCCACCATCCTACAGTCCCGTTCACATCGGCGCAATGTATGGACGCCAGTCCCCTCTTTCCAGAGAACGAGAACGCGACCCGTCACCGGTCCGCTACGACAACCTCTCCAAAACCATCATGGCCTCCATCCAAGAGAGGAAGGAGTTTGAGGAGAGGGAGAAACTAATGCATCGTCACGTTCAAGGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2242
Status:
F2 line generated
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 > G
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000014252 | Nonsense | 501 | 751 | 10 | 11 |
| ENSDART00000129878 | Nonsense | 501 | 751 | 10 | 11 |
Genomic Location (Zv9):
Chromosome 5 (position 19822512)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 17381753 |
| GRCz11 | 5 | 17885749 |
KASP Assay ID:
554-3202.1 (used for ordering genotyping assays)
KASP Sequence:
GAATGCGCTGCTCATCCGGGCGTCCCATCAATGGGGTTTCACTCACCATA[T/G]TTACCCACTAAAATGTGCCATGTTCGTGGACCCGAACTTCAACGCCATGC
Long Flanking Sequence:
ATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAGTTTCATTTTTAAATTGTTTGATTTTTTTTTCTCAAACATTTCCTCTTTCCCTAGATTGTAATGTGCGAGAACGGTAACCCCTCTGCAGTTCTGGAAGAGAGATCTCACGACTACCGTTCGGAGCCCAATCTAGATCTCCCCGACTATCGGAGTGCTCCTCTCCACCGAACATACCAGTCGTCCCCTTTCCAGCTGGACTCCTTTAGCACCACGTCCCGCTCCTTTAGCCTCAAACAGGGAGTAAACCGAGCTGACTGCACACCACTAGGTGGCACCAAGCATGAAACCATCACATCCACCCCTCACAGAGGCGTCTTCTCTCCTGGGACGTTATCCGGCCGCAACAGCAGCCTCTCCTACGATAGCTTGCTAACCCCCAGCGTAGCGCCATCTATAGGCGAATGCGCTGCTCATCCGGGCGTCCCATCAATGGGGTTTCACTCACCATA[T/G]TTACCCACTAAAATGTGCCATGTTCGTGGACCCGAACTTCAACGCCATGCTGGTCCACCATCCTACAGTCCCGTTCACATCGGCGCAATGTATGGACGCCAGTCCCCTCTTTCCAGAGAACGAGAACGCGACCCGTCACCGGTCCGCTACGACAACCTCTCCAAAACCATCATGGCCTCCATCCAAGAGAGGAAGGAGTTTGAGGAGAGGGAGAAACTAATGCATCGTCACGTTCAAGGCTATGCTAATGATTCAGGAGTCTTTGACACCGCGTATGGACTCCCACATGGGTATCCCGACGGTCCTAGAGGCCCCGCGTCTCGAGAGCCCACTCCCCCTGTGTGTGCTTCTAGGGATAACTTGATGGGATATCCTCCTCGGACCCCTGTTTTGCGCTCCTCTGCGTCATCGCTCGTCCGGGCGCCAAGGACTTCAACTACGTCCCTTCACACAGATGGAGGTGGCATGAACAGAACAGCTGAACTACAGTATCGCTCACC
Associated Phenotype:
Not determined