ZMP
zdhhc18
Ensembl ID:
ZFIN ID:
Description:
zinc finger, DHHC-type containing 18 [Source:RefSeq peptide;Acc:NP_001071031]
Human Orthologue:
ZDHHC18
Human Description:
zinc finger, DHHC-type containing 18 [Source:HGNC Symbol;Acc:20712]
Mouse Orthologue:
Zdhhc18
Mouse Description:
zinc finger, DHHC domain containing 18 Gene [Source:MGI Symbol;Acc:MGI:3527792]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa6440 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa22896 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa6440
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000101885 | Essential Splice Site | 231 | 467 | None | 10 |
The following transcripts of ENSDARG00000094201 do not overlap with this mutation:
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 16 (position 36411992)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 34041775 |
GRCz11 | 16 | 33995805 |
KASP Assay ID:
554-5125.1 (used for ordering genotyping assays)
KASP Sequence:
TTTCTGACTTCCTTTATCTTTGGCTGTGTGATCACTCACCTCACTTTGCG[T/C]AAGTTTCAACAGTCACTTTTATACAAWTATAATGTGCCTGCATATRTATT
Long Flanking Sequence:
CTTCTAACTAATTTTATAAATCATTTTTGATATCTGGAATTATATAATACAATAATATGCACAAGTCATATGGAAATTTGTTTGATCATATTTTTTACTGTGCTTCTGCTTTTTTGGAGCTTTAAAATCTCAACTAATTATTTATTGTAATGCCAAAGAAGGAACTTATACATATTTGAAAGCATAAACAATGTTTGTTTTGGGTGAAATATTTCTATAAAGCTTTCGAAGTATTACAGTGTTTTGATAAGTAATGTGCAATAGTTAATTACAGTAACACAGATCACTTCCTCAAAGTAATTTCTTGAGAATTTATTAAAGTGTCCCCCTCTCTCTCTCTCTCTCTCTCTCTTCCTACTAGAGCGCTTCGATCATCACTGTCCTTGGGTGGGAAACTGTGTGGGGAAGCGCAACTATCGCTTTTTTTATGCCTTCATAGTGTCGCTGTCGTTTCTGACTTCCTTTATCTTTGGCTGTGTGATCACTCACCTCACTTTGCG[T/C]AAGTTTCAACAGTCACTTTTATACAAATATAATGTGCCTGCATATGTATTATATGTTTTTATAGACACTACACAACATTTTATGGTTTTTACCATTGATGATAATGATAATAACAAAAAACGTCTTAAACGCCAAATTTTCATGATAGAAAGGATCAACACCAAAGACAGCTTATTTTAAAATTACACTTAAAATTAAAATATTGGCATATTTAATCATTTAATATTTATATATTTATTATATTTGATTATTTTAAATTATAAAATAAAAAAAACATTTATTCTTAACATATTAAAATATATAATTTTTATTTATGTACAATAAAAATATATATTCATTTGTATAAAAGCAAAAGATCATTGTCTTTGTTGTATTTTGATATTTGATAACTTTTTGTAAGCTGTTTCATTTTTTTTCTTTCTCATCAACAGGATCACAAGGTGGGAATGGTTTCATCCAGGCAATACAGGACAGCCCCGCCAGATATCCTTTAAAAGAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22896
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000101885 | Nonsense | 301 | 467 | 8 | 10 |
The following transcripts of ENSDARG00000094201 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 16 (position 36414669)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 34044452 |
GRCz11 | 16 | 33998482 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGATCTTGGTCCAGTAAAAGAGGAGAAGAATCAGGAAATCCATATACCTA[T/G]AACAATATCTTCACAAACTGCTGTGTGGTGCTTTGCGGGCCGATGCCACC
Long Flanking Sequence:
TGCTAATTTATTTATTTATTTTTCCCGCAAAATTCTGTGCAGAGACAGCGAAAAATGTCCATACATTCTGTCTGGCCCTTATGTTACCTTATCTAGATTAGCATGTACCCTTTTTGCGTATTTAAAGATTTAAAGAAAATGAGTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATCTTTATTTTTATATATATATATTATTCTGATTGATATTAATAAATGTGACTTAAACAAGAAAATAAAGTGTAAAATAAAATACCAAATAATGTAAAAGAGGTTACCACCAGCAGGCTAGTTATAAAAAAGAAAAATGTTTATTATGCACATCTTTTGCTTTCCCTCTCTCCACACAAATCTTTTAAATTTGATTTCTCTTTTTCCTTTTAATGATTGTAGATCAAAGGATCTTGGTCCAGTAAAAGAGGAGAAGAATCAGGAAATCCATATACCTA[T/G]AACAATATCTTCACAAACTGCTGTGTGGTGCTTTGCGGGCCGATGCCACCCAGGTCAGTACTGCATGCACAAGACAACGTCATGGCAGATATTAAATTCAGAATTCTGACATTTAAAGATTAGTGAGCAAATGAAGAACTTCTTTAGCTTCAGGCTAATGTGTGTCCTGGGTTAAGCACATACTGTTACAAACAACAACAAATATGCTAAGTACAGTCTGTGCCGTGTTTTTAAAGTCACAATAGGTCACATCCTTGTCATCTTTTGCAGCTTGATTGACAGAAGAGGCTTTGTACCTCCAGAGGACGCACCTCAAACTGTGACCTCTGACGCTGAGCTCCCTGCTTTCATGGCCAAAAATGACACAAACATGGTGAGAGAATGCCGTTTAAAAAATAGTTTCAAGTATTGTGGCTGTGGTTTTTAAAATCCTCAAAGCATAAAAAGCATTCCATTGCCTTTCAAGCCCTAAACTACAGTTCAAAGAAAAAAAGAAATCT
Associated Phenotype:
Not determined