ZMP
zgc:63934
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC393316 [Source:RefSeq peptide;Acc:NP_956639]
Human Orthologue:
ZDHHC16
Human Description:
zinc finger, DHHC-type containing 16 [Source:HGNC Symbol;Acc:20714]
Mouse Orthologue:
Zdhhc16
Mouse Description:
zinc finger, DHHC domain containing 16 Gene [Source:MGI Symbol;Acc:MGI:1921418]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa30954 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa35182 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa30954
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000005789 | Nonsense | 33 | 386 | 1 | 11 |
| ENSDART00000114854 | Nonsense | 37 | 239 | 2 | 9 |
Genomic Location (Zv9):
Chromosome 12 (position 3439003)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 12 | 2826003 |
| GRCz11 | 12 | 2860736 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTCTGTCCTCGTCGGGGACACAGAAAGCGCAGCAGAGTCCGAGACCTGT[G/A]GAATTATGGGATGGTGGTGCTGAAGTCCCTCTACTACAACGTCCAGACCA
Long Flanking Sequence:
ATAAAAAAAAAAAAAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATGAAGAAGTCAATTAAGCAAAAGAATGTGTGTATATATATATATATCAAAAATGTCCTTTTATAATGTCTGTGTGTTTTATATTGTCATTTTTTTGCCTTTTATTGGGAATGAAATTCATTCTTATATTTTATAATAATAATAATAATAAGAATAAGAAAATAATAAGAAAACTAATAAGAAAAAAATGCATTATTTGACTATTATAAACAACTAATTAGGTAATATGTGGTTGTTGTCAATTCTTAATCACTACTTATTTACTGTGTGTGTCTGTGTGTGCGTGCATGGGTTTTAGGGGGATGCGCAGCTGGAGGTGGTCCGTCTCCAGGATCATGCGTCTCTTCCTGCGCTGGTTCAGACTCTGTCCTCGTCGGGGACACAGAAAGCGCAGCAGAGTCCGAGACCTGT[G/A]GAATTATGGGATGGTGGTGCTGAAGTCCCTCTACTACAACGTCCAGACCAATTCAGACACGGTGCTGGACTGTATGTTTGAGCCCATCTACTGGCTAGTGGACAACATGACCCGCTGGTTCGGAGTGGTACATAACATTCATCTTTTTAATACAGCATTTTATTCGAATTAAAACATGTTGTTGTTATTAATTATTCAAATCAATTGCAAAGTAATGAAATTTAACTGAGAAATCGCCACTAGAAAGAAACGTGGAAGTTGTTATGATGTCTGGTGTGTGTTTCCTCCATCCAGGTGTTTGTGTGTCTGGTGATGGCCTTGACCAGCTCAGTGGTGGTTATCGTGTATCTGTGTGTTCTGCCCATCATCTTCAGCTCATATCCCGTTTACTGGATCCTCTGGCATCTGTGTTACGGCCACTGGAATCTGCTCATGGTCGTCTTTCATTACTATAAAGCCACGACCACACAGCCTGGATTCCCTCCGCAGGTGCTGCACTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35182
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 |
|---|---|---|---|---|---|
| ENSDART00000005789 | Essential Splice Site | 140 | 386 | 2 | 11 |
| ENSDART00000114854 | Essential Splice Site | 144 | 239 | 3 | 9 |
Genomic Location (Zv9):
Chromosome 12 (position 3438512)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 12 | 2825512 |
| GRCz11 | 12 | 2860245 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTTCATTACTATAAAGCCACGACCACACAGCCTGGATTCCCTCCGCAGG[T/C]GCTGCACTACGTTACACTTGTTTTTGCACAGTCTAGTTCACATTTGAAGT
Long Flanking Sequence:
GAGACCTGTGGAATTATGGGATGGTGGTGCTGAAGTCCCTCTACTACAACGTCCAGACCAATTCAGACACGGTGCTGGACTGTATGTTTGAGCCCATCTACTGGCTAGTGGACAACATGACCCGCTGGTTCGGAGTGGTACATAACATTCATCTTTTTAATACAGCATTTTATTCGAATTAAAACATGTTGTTGTTATTAATTATTCAAATCAATTGCAAAGTAATGAAATTTAACTGAGAAATCGCCACTAGAAAGAAACGTGGAAGTTGTTATGATGTCTGGTGTGTGTTTCCTCCATCCAGGTGTTTGTGTGTCTGGTGATGGCCTTGACCAGCTCAGTGGTGGTTATCGTGTATCTGTGTGTTCTGCCCATCATCTTCAGCTCATATCCCGTTTACTGGATCCTCTGGCATCTGTGTTACGGCCACTGGAATCTGCTCATGGTCGTCTTTCATTACTATAAAGCCACGACCACACAGCCTGGATTCCCTCCGCAGG[T/C]GCTGCACTACGTTACACTTGTTTTTGCACAGTCTAGTTCACATTTGAAGTGAGCTGTGATTTGCATGTTAAGGAAGCCATATGTGTTTAGTTTACATTTATGCAGTTGAGAAAAACACAATGCACAAACAATAATAAACTCCTGTTGTCAAAAATAAATTGCAGAAGAGATGGCTTATGTGTTTATGGGCTAATGGTATTCATTCATTCATTCATTCAATCCTTTTCTTGTCGGCTTAGTCTCTTTATTAATCTGGGGTCGCCACAGCGGAATGAACCGCCAACTTCTCCAGCAAGTTTTTACGCAGCGGATGCCCTTCCAGCCGCAACCCATCTCTGGGAAAAGCTAATGTTATTTTTAAGCTAAAATTAGTATTCTCGTTTGGTTTAATAAAGGAACATAAATGCCTTCAATAAAATTGTACACAGTTAATACGGTTGATATAGGTATAAAAATAATAAAACAACAAATCTTTAGAAAGTGAAGGGGAAAATTGCAAT
Associated Phenotype:
Not determined