ZMP
wu:fi22e09
Ensembl ID:
ZFIN IDs:
Description:
zinc finger, DHHC-type containing 13 [Source:RefSeq peptide;Acc:NP_001008650]
Human Orthologue:
ZDHHC13
Human Description:
zinc finger, DHHC-type containing 13 [Source:HGNC Symbol;Acc:18413]
Mouse Orthologue:
Zdhhc13
Mouse Description:
zinc finger, DHHC domain containing 13 Gene [Source:MGI Symbol;Acc:MGI:1919227]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa13890 | Nonsense | Available for shipment | Available now |
| sa17046 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa13890
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:
C > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000103361 | Nonsense | 19 | 645 | 2 | 17 |
Genomic Location (Zv9):
Chromosome 7 (position 17287674)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 16261009 |
| GRCz11 | 7 | 16512982 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CMTTGTAAAAATTTACAGTCCCACTCCCATGGKCACATGGGTGACAGTTG[C/A]CATGGACATGGCGGTGGCCACTCCCATGGACACGGACACAGTCATGGAGG
Long Flanking Sequence:
AACTCTTGCATATCCTGTAGATAATATTTCAAACAGTGCATTTCTTACATCTTCTGTAAACAATATTTTAATGTAAATAATAATTTAAATGTAATGCAAGTATGCCGTCTTAAGGCATCTCTGATGCAGCTCCCAATCAACGTCAATTTAGTGCAAACGCGCAATGTGTAGTAATATTTTTTTTAAGAGGTGCACAGGTATGCGACCGCGGGAAGGCTGCGCTGGACTACACCTGTGTGTTCGACGCAGAAGTATAAATCAGAATGGAATTACATGACTCCACACGCAGTAGGGAAAGTAATTGAAAAATTTGACTTGTAAAAATTAAATCGATTATAGATTCTGGATATCGATTTTGATTATTTTTCGATGAATCGCTCAGCCCTAGTTTGAATATTGCCATATCAAATCCAATTGGCTTTAAATTTGAAATCACTAATCGTGAATAACCCTTGTAAAAATTTACAGTCCCACTCCCATGGTCACATGGGTGACAGTTG[C/A]CATGGACATGGCGGTGGCCACTCCCATGGACACGGACACAGTCATGGAGGATCTGGGTTTGGTGGTTTCATGCCCGCTGGCTTCCACGGTCAGCTTGTCCCGGGACCTATGGACCCCACACAGCAGCCGAGGAAATCCTCGCACCCCGAGGACAGCAGCTCCTGGGACATCATCAAAGCAACACAGTGAGATTTATTCCCTACATGTGCAGTAAACACTATAATATTCACATGGGAAATATTTAGCTGTTAATATTTTATGGTATTAAGATGCCCCGGGGAGTTTTGGTCACAGCTGTAGGGAAGTATATTTGTGTGATGCTATGAATTAGTTTAAGTGCGATTTCAACAATAAATACTGACTTTAAGGATGCTTCACCCAAAACTAATTTTAAATAATTCACTTTCTTGGGATTTGCTTGTATTGTCATATTTTGAAATATATTTTAGACATTTCAAATGTATTTTAGGTGATTTGGTAATAATTAATTAATGCAGTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17046
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000103361 | Essential Splice Site | 434 | 645 | 11 | 17 |
Genomic Location (Zv9):
Chromosome 7 (position 17309777)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 16282978 |
| GRCz11 | 7 | 16534951 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGAACTGACCCAGGAYACGTCAAGGCCACCGAGGAGGARAAGAARAAGG[T/A]AAGAGCGGCCTGGCAGTGGCNNNNNNNNNTGTTCATCTAATTGCACAGTAGAKATGCTG
Long Flanking Sequence:
AAAATCGTACACATACCGTAGGAACGGCATTACAGAAAATGTTGGCGGTTTTAAAACCTTGACTTTTCCAAACTGTGGTATACCTTGAAAACAGTTATTGTCCCATGCCATTGCAAAATAACTAGTAAAGTGTTATGTACTGTCATCATGGCAAAAGCAAAGTAACTTAAGCAACTTAACTTATTGGAAATGTAATTAATAAAATTGTGTTATCTTCTTGTAGATTCATTGATGAATTAACTTTGGTTTTGAATTTAACAGTCTTTGCGATTTTCTTATTTATAAACCAAATTGCTTTATGAATGAGTGTGAATGTATATCATAATCATTTTGTTGACCATTGTTCATTGCCTTGACCTGTATGTTGGGGTCACATGAGCCCAGCGCTGCAGTTCAGATGCTCTTCACTGTCAACATCACTGCTGTGCTCTACTACTACATCCGCTCCTGCAGAACTGACCCAGGACACGTCAAGGCCACCGAGGAGGAAAAGAAAAAGG[T/A]AAGAGCGGCCTGGCAGTGGCTGTTCATCTAATTGCACAGTAGAGATGCTGGGGTCATTGTGGAGACAGATTCTGATTGGTTGGTCTGGATGGGAAGTTCTTTCTGGTTTGAGAAGTAACTTAAATTCACTTGAGAGTATTGCAAACTTGTGGTTTAACTCGTTTGGCCAGCGGAGAAATTAAAATGGTCGTGCCCAACTGAGTCTGGTTCTCTCAAGGTTTTTTTTCTTCACTCCCATCAGGTGAAGTTTTTTTTCCCTCTACGCTGTCGCCACTGCCTCGCATGGTTCAGGATTGGTAGAGCTACGCATCGATGAATTTGCTCTTCAGTGTTTGAACTCTCAGTAATGATTAAATCACACTGAACTGAGCTAAACTGAACTGAACTGAACTTAAACACTAAAACCTGAACCACACTGTTCCAGTTACTATGACCATTTATGTGAAGCTGCTTTGACACAATCTACATTGTAAAAGCGCTATACAAATAAAGCTGAATTG
Associated Phenotype:
Not determined