ZMP
zdhhc23
Ensembl ID:
ZFIN ID:
Description:
probable palmitoyltransferase ZDHHC23 [Source:RefSeq peptide;Acc:NP_001003757]
Human Orthologue:
ZDHHC23
Human Description:
zinc finger, DHHC-type containing 23 [Source:HGNC Symbol;Acc:28654]
Mouse Orthologue:
Zdhhc23
Mouse Description:
zinc finger, DHHC domain containing 23 Gene [Source:MGI Symbol;Acc:MGI:2685625]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa24490 | Essential Splice Site | Available for shipment | Available now |
sa3265 | Essential Splice Site | F2 line generated | Not yet available |
sa37877 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa24489 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa24490
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 |
---|---|---|---|---|---|
ENSDART00000010126 | Essential Splice Site | 46 | 425 | 2 | 5 |
Genomic Location (Zv9):
Chromosome 24 (position 21738957)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 20986086 |
GRCz11 | 24 | 21130505 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGGTGGCATGTTGCTGTGACTGTGAGGATTTGGATGAGGCTTGTGACAG[G/A]TGAGTGAAAAAAATCTAACTGTGGGTTAAAGTATTTATATTTACATGAAA
Long Flanking Sequence:
TCGTTTATTATTTAAAATGTTAGTGCTGTCAACAAGTTTTGAAATTTTTTATGTTAATTGCACTCATTATTTTTTTAAAACTTAATTAAAAAATGTCTTTATCATAATCTTATTACTTTACATTAGACAAGACTCCAGTCTTTAATTCGAAGAGAATATTGTATTAGGAAATTTCCTATAAAGATGATTAATTCATATCATTTTAGGATTTGCCAGATTAATGACCACAGAATATACAGTGTCTGTCTGCCCATTAGTCGGTCTCTGCCATACAGTACTAATATACTGAGACATGCATCTGAACTGTAAACTTGTTTCTCTTACAGGAATGCGGTCTCTTTGTTTTATGAGTTGATGTCCATCATGAAGAAGAGATCTAGTCGAGCAGCAGATCCGGATGAACTTCTGTGCTGTTGTGAGTACATTGACCGTCATGGCAGTCGCAGTCACATGGTGGCATGTTGCTGTGACTGTGAGGATTTGGATGAGGCTTGTGACAG[G/A]TGAGTGAAAAAAATCTAACTGTGGGTTAAAGTATTTATATTTACATGAAATAAAATGGCAAATGGTCATCATTTGCTCACATGTCGTTCAAAATCCATATCACTTTCATGGCTGCACCTAAATAGTGGAATGTGCTGCCTTTGTATATTAGACAAGCCTCTTCAATTACCGGTTTTGAATATCTTTTTAAAACCTACTTGTTTAATTTGCCGTTAGAACATTTTATGTTTATTTATTTGTATTTATTTTCTGACTGATTTAGTTTGACAAGTGTAATAACAATAAAATAAATCAAAACAAAACCACAGATTACAAAAGCAATGGCAACTAACAAACGGACCCAAAGTGTGCCAAGAAAATATCCACCACATCATTACACCACCACCAGCCCGAACCGTTGATACAAGGCAGGATGGATCCATGTTGACGCCAAATTCTGACCCTACCATCCGAATGTCACTGCAGAAATCAAGACTCATCAGACCAGGCAACGTTTTTCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa3265
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000010126 | Essential Splice Site | 279 | 425 | 4 | 5 |
Genomic Location (Zv9):
Chromosome 24 (position 21734808)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 20981937 |
GRCz11 | 24 | 21126356 |
KASP Assay ID:
554-2959.1 (used for ordering genotyping assays)
KASP Sequence:
TGACCCTGTGTGTAAGTGATCTGTGTAAATGAAGCTCAGTGTCTGTTATC[A/T]GGATCAACAGTTGTGTYGGACTGGCCAATCACCGCACTTTCCTTCTGACG
Long Flanking Sequence:
ATACACTATGGACGATTTAGCTTACCCAATTAAGTTATTTAGCGCAAGTCTTTGGACTTGTGGGGAAAACTGGACCACCCAGAGGAATCCCAAGCGAACACGAGTAGAACATGCAAACTCCACATGGAAATGCCAACTGACCCAGCCAAGGCTCAAACCAACGACCTTGAGGCGATTGTTATCCACTATGCCACCGTGACACCCTCCACTTAAAAATATTGAGTTAACCAATTTGTGTTGGGACAACATGGATGAATTGAGTGGAACCATGCGTTTTATTACAGTGTAGGATAATACTGTGGAAATTTCCTCGAGGGCTAATATTTAGCCTTCAACTGTATATACTGATATATATTCTAACAAGCCATTTTTGAAATATAGTTGGATTAAAGTGCATTGAAGTGCCTGCTAAATGTGTTGTTCTTCCTGTCAGCCTGTGTGTAATAGACCTGACCCTGTGTGTAAGTGATCTGTGTAAATGAAGCTCAGTGTCTGTTATC[A/T]GGATCAACAGTTGTGTTGGACTGGCCAATCACCGCACTTTCCTTCTGACGCTGCTCTTCTTCCTGCTGACGTCGATTTATGGCATCAGTCTGGTTCTGGCAAGTGTGTGTCCTGATCAGAGAGTCTTGACTGCTCTCTTCTACTGTCCCGATGTCTACAGTCAATACAGGTGAAAAAACACACACACACAAACACAAACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACTTCTCTTTGTATTCACTGCCTCTGTTCCTTCCAGTTCATTAGATATTCATGGAAAAAGATGTTTTTCCCCTCTGAAGCATCACTTTGAATCGTCAATTTAATGGGGTTTTGTTGACTTTTTGCTTCAAATGCACCGCATCAATTTTTATCTCCATAGCAGAGCGCAGAGAAGAAAATGAACACAAATCCCTTTTCTAAACATCATCTGCTGCTCTCCACATCAACATCAAGGCCTGCTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37877
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000010126 | Essential Splice Site | 335 | 425 | 4 | 5 |
Genomic Location (Zv9):
Chromosome 24 (position 21734638)
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAGTCTTGACTGCTCTCTTCTACTGTCCCGATGTCTACAGTCAATACAG[G/T]TGAAAAAACACACACACACAAACACAAACACACACACACACACACACACA
Long Flanking Sequence:
GGCGATTGTTATCCACTATGCCACCGTGACACCCTCCACTTAAAAATATTGAGTTAACCAATTTGTGTTGGGACAACATGGATGAATTGAGTGGAACCATGCGTTTTATTACAGTGTAGGATAATACTGTGGAAATTTCCTCGAGGGCTAATATTTAGCCTTCAACTGTATATACTGATATATATTCTAACAAGCCATTTTTGAAATATAGTTGGATTAAAGTGCATTGAAGTGCCTGCTAAATGTGTTGTTCTTCCTGTCAGCCTGTGTGTAATAGACCTGACCCTGTGTGTAAGTGATCTGTGTAAATGAAGCTCAGTGTCTGTTATCAGGATCAACAGTTGTGTTGGACTGGCCAATCACCGCACTTTCCTTCTGACGCTGCTCTTCTTCCTGCTGACGTCGATTTATGGCATCAGTCTGGTTCTGGCAAGTGTGTGTCCTGATCAGAGAGTCTTGACTGCTCTCTTCTACTGTCCCGATGTCTACAGTCAATACAG[G/T]TGAAAAAACACACACACACAAACACAAACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACTTCTCTTTGTATTCACTGCCTCTGTTCCTTCCAGTTCATTAGATATTCATGGAAAAAGATGTTTTTCCCCTCTGAAGCATCACTTTGAATCGTCAATTTAATGGGGTTTTGTTGACTTTTTGCTTCAAATGCACCGCATCAATTTTTATCTCCATAGCAGAGCGCAGAGAAGAAAATGAACACAAATCCCTTTTCTAAACATCATCTGCTGCTCTCCACATCAACATCAAGGCCTGCTCAAATATTAGAACTTCTGCTTCTGAGAGAAGTTGCGGGTTATTTTACAATATATAAATTAATAATTACACTATTTTACACAATATATAAATATTTAATTTTTAATTCACACATTTTATTATCCAACTGCTTGTTAATGAAATTCTAATCCCAGTTTCTTTGCAAATCCTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24489
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000010126 | Nonsense | 398 | 425 | 5 | 5 |
Genomic Location (Zv9):
Chromosome 24 (position 21731487)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 20978616 |
GRCz11 | 24 | 21123035 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCGCTCAAAGGCGCCTCTGGGGTCTCATCGTCCACACCGGCCATTATTCC[A/T]GAGGCTTCTGGAGCAACTGGACTGAGTTCTTGACCATGACTGAAGATACA
Long Flanking Sequence:
TTTAGCTCATATTTGAATTGTCAAAGACGTCAAGGTATTTGTGGTATCTCAAGTCTTACAGTGCCTTTTAAAGTTCTGTTCATCCCCACACAGCTCTTTAAAGGGCACATAGTTTACCCCTTTTTATGTTTTAGTATTATTGTTATGGTTCTTCTGAGTGTGCCAGTTTAGGTTCAGTTCAAAACACAGTTCAGATTATTTTATTATAATGTGTTAATATGACTCTTCATAGCATTAGACTGCTCATGTTTAGTATTCAGCATTCTATTAATAATAAAGTGTTCAATAATGAGCTGTTTGTTTGCGTGTTCAGTTCTGCGCTGTGCTTCACCTGTGCCTGGTACAGCAGTATCGTGACTGGAGGTTTGCTTCACCTGCTGCTCCTGCAGATCCTCAACATCAGCCTGAACGTGACAGAGCGAGAGGCACGTCTGGCCCTCAGAGAGAAGAGCGCTCAAAGGCGCCTCTGGGGTCTCATCGTCCACACCGGCCATTATTCC[A/T]GAGGCTTCTGGAGCAACTGGACTGAGTTCTTGACCATGACTGAAGATACACAGCCAGCAGGGCACAAAACAGAAGATTTGGTGTAGAAACTGAGCATTTATACAGTGACTAGCATAAATGAGAACATCATCTGTTAAACATTTCTTTGAGAATATGGAAATACAGTTTTATTAAACAGTTCTATTTATTAACATAAAAAGTGGTGACCGATCATATTTAGGATAAGGAAAATAATATAAATATGATATAGAATTTCCTACAACTCTTTGTCTGACTTAATTTTTTAAAATCACAATCATATGGTGTGTACTTATTTTTGCACAATGATCTTAAATTATTTTGAAAGATTAATTCCTGTTTTGGCTTTGGTACTGACTAATCTTATGGAAAACCAATAACCCAAATTTGCACAAATATCTCATTGCATGGCATTCCATAGAAAGAATTAAAGGGATAGTTCACCCAAATATGAAAATTCTGCCATCTTTTACTCACCCTTC
Associated Phenotype:
Not determined