ZMP
dnajc18
Ensembl ID:
ZFIN ID:
Description:
dnaJ homolog subfamily C member 18 [Source:RefSeq peptide;Acc:NP_001107060]
Human Orthologue:
DNAJC18
Human Description:
DnaJ (Hsp40) homolog, subfamily C, member 18 [Source:HGNC Symbol;Acc:28429]
Mouse Orthologue:
Dnajc18
Mouse Description:
DnaJ (Hsp40) homolog, subfamily C, member 18 Gene [Source:MGI Symbol;Acc:MGI:1923844]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa9193 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa37341 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa9193
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 |
|---|---|---|---|---|---|
| ENSDART00000101054 | Nonsense | 179 | 407 | 4 | 8 |
Genomic Location (Zv9):
Chromosome 21 (position 28991591)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 30210835 |
| GRCz11 | 21 | 30247530 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATTYAGCTATAGGCAATGCWTATGCWGTGCTCAGTAACCCAGAGAAAAGG[C/T]AGCAGTATGATGAGTATGGAGACCAGGGCCCTGCCGAAACATCCAGTCAG
Long Flanking Sequence:
TGATGAACTGTTTTCCAGTTTCGGCAAGAGGATTTCTCCTCGACACACCAACAACAGGCACAACGTCATAATGACTCCCCTACATGGCAAGTTTATGACTGGTTCATGCGGCTCATATTACTGCTGAAGTTCTGATTTTCGTGCGTCAAACTTGCGCTGCTTCATACGCACAAATGACGTGTGAACGAATCGCGCCTCAGGATGTCTGTTCGTGTCTTTGCATTGCAGAATTAGTGCATTAAAACAAAAAAATGTAAGTTGTAGCAATACTTCGTGATATTAATATCTTCAATTCAATTTTATTGCTAGACAGTCTTGAGCAGAAGAGATTTCTGACAGATCCAAACATTTAGATTTACCTATTACTTAAATAATACATTACATTTGTTAGATATTGCTTATCATATACATGCATAGCTTAAAAATTTGTTTTCTACTCCCCCCTTTTCTATTTAGCTATAGGCAATGCATATGCAGTGCTCAGTAACCCAGAGAAAAGG[C/T]AGCAGTATGATGAGTATGGAGACCAGGGCCCTGCCGAAACATCCAGTCAGCCTTCAGCCCAGCCGCGTCAAGCATACGCACGCCATCGCTCTTTCACCAGAGACTTTGAGCCTGACATCTCCCCCGAGGAGCTCTTCAACATTTTCTTCGGTGGCAGGTTTCCCACAGGTATGACCCTCTATTAAACACTACAGCTAACTAAATGGATCACACGTAGTTAGAGGCTTTTTTATGTACATGTCATTAAAAGAAGTATTTAATTTCTGCATCCTGTAAAAGTCATGAGCTGATACTAACTAAATTTTTCAGGTTGCTCTTTTGGAATGGTTTCATCAAATTTCTGTGCTCTCAATTAGGGCTGCACAGGGTTATGTGTGCATTTTGTCAGTAAAGCTGGTTCTGTAATCAGCTGTTAATCTTTAGCATTTGCTTTCAGATGTACTATCATTCATACTATCATGCTTATATATTTTGCTTATATTTTTGTTTTCCAAATTTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37341
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 |
|---|---|---|---|---|---|
| ENSDART00000101054 | Essential Splice Site | 234 | 407 | 4 | 8 |
Genomic Location (Zv9):
Chromosome 21 (position 28991422)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 30210666 |
| GRCz11 | 21 | 30247361 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCCCCCGAGGAGCTCTTCAACATTTTCTTCGGTGGCAGGTTTCCCACAG[G/A]TATGACCCTCTATTAAACACTACAGCTAACTAAATGGATCACACGTAGTT
Long Flanking Sequence:
ACAAATGACGTGTGAACGAATCGCGCCTCAGGATGTCTGTTCGTGTCTTTGCATTGCAGAATTAGTGCATTAAAACAAAAAAATGTAAGTTGTAGCAATACTTCGTGATATTAATATCTTCAATTCAATTTTATTGCTAGACAGTCTTGAGCAGAAGAGATTTCTGACAGATCCAAACATTTAGATTTACCTATTACTTAAATAATACATTACATTTGTTAGATATTGCTTATCATATACATGCATAGCTTAAAAATTTGTTTTCTACTCCCCCCTTTTCTATTTAGCTATAGGCAATGCATATGCAGTGCTCAGTAACCCAGAGAAAAGGCAGCAGTATGATGAGTATGGAGACCAGGGCCCTGCCGAAACATCCAGTCAGCCTTCAGCCCAGCCGCGTCAAGCATACGCACGCCATCGCTCTTTCACCAGAGACTTTGAGCCTGACATCTCCCCCGAGGAGCTCTTCAACATTTTCTTCGGTGGCAGGTTTCCCACAG[G/A]TATGACCCTCTATTAAACACTACAGCTAACTAAATGGATCACACGTAGTTAGAGGCTTTTTTATGTACATGTCATTAAAAGAAGTATTTAATTTCTGCATCCTGTAAAAGTCATGAGCTGATACTAACTAAATTTTTCAGGTTGCTCTTTTGGAATGGTTTCATCAAATTTCTGTGCTCTCAATTAGGGCTGCACAGGGTTATGTGTGCATTTTGTCAGTAAAGCTGGTTCTGTAATCAGCTGTTAATCTTTAGCATTTGCTTTCAGATGTACTATCATTCATACTATCATGCTTATATATTTTGCTTATATTTTTGTTTTCCAAATTTGATTATCCGTTTTTATATTTTACCTGATATCGATGTTGTTTTAAATATTTGTTTATGCTTGTGAAGCACTTTAAGTTGCATGTTAAGTAGAAAAAGTGCTATACAGATAAAATGTATTATTATTAATATTATGATTATGATTATGATTATGAAAACAGTTACCTCTTCTCT
Associated Phenotype:
Not determined