ZMP
zgc:153638
Ensembl ID:
ZFIN ID:
Description:
dnaJ homolog subfamily B member 14 [Source:RefSeq peptide;Acc:NP_001071255]
Human Orthologue:
DNAJB14
Human Description:
DnaJ (Hsp40) homolog, subfamily B, member 14 [Source:HGNC Symbol;Acc:25881]
Mouse Orthologue:
Dnajb14
Mouse Description:
DnaJ (Hsp40) homolog, subfamily B, member 14 Gene [Source:MGI Symbol;Acc:MGI:1917854]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa6592 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa39625 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa6592
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000102337 | Essential Splice Site | 45 | 380 | 2 | 8 |
Genomic Location (Zv9):
Chromosome 1 (position 26845767)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 27182912 |
| GRCz11 | 1 | 27876626 |
KASP Assay ID:
554-4979.1 (used for ordering genotyping assays)
KASP Sequence:
CCAGATAATTTTACTTTTTTTTTACATTTTGCTTGTTTGGCTTTATTGGC[A/T]GTATTGTTGGAAGCTTTGCTGAACAATGGAAATTCGACAGGAAACARTAC
Long Flanking Sequence:
GTTTTAAGGATCTGTACTTGTTCATAATTGTTTTAAATAAGCTATTATTTTATTAGTAAGCCATTTTACATTATCATTGATCTGTAGCTATAATAAAATATTTTTAAATTGAATAATTAAGATTTATGCATAAGTATTTATGTATATAAACTAAAGCATTTGTTTAGTAAGAAGTGCTTCTCATATGATATGTGAACTCCAAGCAAGAATGACGTCAACTGCAACTTTTCCAACTTTTCACCAAAAGGGTACCACTGGTACCATATTGCAGTAGAGACACAACTCTGATAAAGGTGACCCGTATCATACAGTTCCACTCAGTGGAAACGAGGCATATGAGAGTATCTCAGATCATACAATGGGAAGACGACCTGCATTTTTTTTTTTTTTTTTTTTTTTTGTTAAACCCCTAGTGTTTTTCTAAATTAGATAATAGGATCATTTAATTTGCCAGATAATTTTACTTTTTTTTTACATTTTGCTTGTTTGGCTTTATTGGC[A/T]GTATTGTTGGAAGCTTTGCTGAACAATGGAAATTCGACAGGAAACAGTACTGCATACTGTGGGAAGTCATCAAATGGATCAAAGCCTGGATCACAAACCCAACATGAGGCACCAAAGCAAGACTCAGCAGCTGCAGATTTAACAAAAGGATTTACCAAAGAGCAAGCTGAAGGGGTACAAAGGCAAGTATTCTTGTGTATTCATTAATAGGTCCATAACCCAGAAAGTGTCGTAGTCCCTATTGCATTCCTTTAGTCAGCGCTTCTCAGCCAGGATTCAAGAGCCCAAAAGATTGATTGATTAATTGACTCGTTGTCAGATTTATTCAAGAATTGAATAATTTTCGGAACTTAAGCACACCTAAAATAGAACATTCCAAATTTGCTTGCAAGATATAGCATCTCTATACATTAAAATCGTATGTGTGGGTGTGTGTTGGTGTGTGCGTGCGTGCGTGCGTGCGTGCGTGTGTGTGGGTGTGTGTTTTTTTTTTTAATATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39625
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 |
|---|---|---|---|---|---|
| ENSDART00000102337 | Nonsense | 76 | 380 | 2 | 8 |
Genomic Location (Zv9):
Chromosome 1 (position 26845861)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 27183006 |
| GRCz11 | 1 | 27876720 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAGTACTGCATACTGTGGGAAGTCATCAAATGGATCAAAGCCTGGATCA[C/T]AAACCCAACATGAGGCACCAAAGCAAGACTCAGCAGCTGCAGATTTAACA
Long Flanking Sequence:
AAAATATTTTTAAATTGAATAATTAAGATTTATGCATAAGTATTTATGTATATAAACTAAAGCATTTGTTTAGTAAGAAGTGCTTCTCATATGATATGTGAACTCCAAGCAAGAATGACGTCAACTGCAACTTTTCCAACTTTTCACCAAAAGGGTACCACTGGTACCATATTGCAGTAGAGACACAACTCTGATAAAGGTGACCCGTATCATACAGTTCCACTCAGTGGAAACGAGGCATATGAGAGTATCTCAGATCATACAATGGGAAGACGACCTGCATTTTTTTTTTTTTTTTTTTTTTTTGTTAAACCCCTAGTGTTTTTCTAAATTAGATAATAGGATCATTTAATTTGCCAGATAATTTTACTTTTTTTTTACATTTTGCTTGTTTGGCTTTATTGGCAGTATTGTTGGAAGCTTTGCTGAACAATGGAAATTCGACAGGAAACAGTACTGCATACTGTGGGAAGTCATCAAATGGATCAAAGCCTGGATCA[C/T]AAACCCAACATGAGGCACCAAAGCAAGACTCAGCAGCTGCAGATTTAACAAAAGGATTTACCAAAGAGCAAGCTGAAGGGGTACAAAGGCAAGTATTCTTGTGTATTCATTAATAGGTCCATAACCCAGAAAGTGTCGTAGTCCCTATTGCATTCCTTTAGTCAGCGCTTCTCAGCCAGGATTCAAGAGCCCAAAAGATTGATTGATTAATTGACTCGTTGTCAGATTTATTCAAGAATTGAATAATTTTCGGAACTTAAGCACACCTAAAATAGAACATTCCAAATTTGCTTGCAAGATATAGCATCTCTATACATTAAAATCGTATGTGTGGGTGTGTGTTGGTGTGTGCGTGCGTGCGTGCGTGCGTGCGTGTGTGTGGGTGTGTGTTTTTTTTTTTAATATGCAGTTTATTTTTCAAAAATGCTAGGGCCCCATACCTCTATGTTTTCCAGCAAAATAGTGTGATTATCGCCAGCTGTTAGTTCACCATGTCCTGC
Associated Phenotype:
Not determined