ZMP
zgc:77513
Ensembl ID:
ZFIN ID:
Description:
dnaJ homolog subfamily C member 4 [Source:RefSeq peptide;Acc:NP_997842]
Human Orthologue:
DNAJC4
Human Description:
DnaJ (Hsp40) homolog, subfamily C, member 4 [Source:HGNC Symbol;Acc:5271]
Mouse Orthologue:
Dnajc4
Mouse Description:
DnaJ (Hsp40) homolog, subfamily C, member 4 Gene [Source:MGI Symbol;Acc:MGI:1927346]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa42346 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa35636 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa42346
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 > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000038847 | Essential Splice Site | None | 237 | None | 9 |
| ENSDART00000102647 | None | None | 237 | None | 6 |
| ENSDART00000148210 | Essential Splice Site | None | 237 | None | 8 |
The following transcripts of ENSDARG00000024090 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 14 (position 8445766)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 14 | 8169010 |
| GRCz11 | 14 | 8475124 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAAGCAACAGAACATCCACAGCTGACCTGCGCGTCTCCATGAATGAAGG[T/G]GACGCCATTATTTATGTTTAATCCGCTGATTAATGACTTACTAATAAGAA
Long Flanking Sequence:
CCATAGTAAAGCGCTAACATTAAATTTGCAACATTACAACAGCATACTGTCGTAATAACTATATAGTGATAAACTAACAAATACTGTACTAGGCCCATACTTTAGTTTTTACTGATATTAATATGCAATGTTTTAGAAAAATGTGTACAGTATTGGGTAAATTGCTTGTATTACTATAATTGTATTACTACAATAACTATAGAACAACAGATTAATTCAATTACTTTACTATGGTTAAAAATATAGTATTTATTTATTTGCTCTAATATTAGTACATTTAGTATATAGTACTCTTTATAATATATTAATATATTACAGAAATATCCATTACTATATTATGTTATTCATGTAAATAACCCATTCAGAACAGGTATGGTGCAAACAGTTCCTGACATGCAGCTGTCATGAAACACATTGTCCATTTATGTAACAGCACTTGTGAAGCGTTATGAAAGCAACAGAACATCCACAGCTGACCTGCGCGTCTCCATGAATGAAGG[T/G]GACGCCATTATTTATGTTTAATCCGCTGATTAATGACTTACTAATAAGAATTACACTGATTTGAACAGCAGTCGTGTGCTAAGCTACACGTTTCCCATGACTTTGTTGTTGTTTTTAGCATCGCGGCTAAGCTAGCGAGTGGAAAGTGCATCTCTGTCACAGGAACTGATTAATATGCCTCAAAACATGTATGAGTTGCGTTACGAATTCTTTATATACGTTATAAAATCGTGTCAATACAGTTTAGATTTTAACAACAGCCTTGCTGTCGTTGCCTGCTAATTTGAGTTTGCTGATCAATGGACGTGTCTCAAAAGTGTGGTGACTACATAGACAGCACTTTTGGGCGCATTTGTGGTTATGTTTTGCGGGGTGAAAGGCTGTATAGATTGTTAGCTCAATATATTCCCACATGATAAAATACTATAGGACGTTATAGTAAGTATTATAGTGTTTTTAACCATACTACTGTATAGTAGTGTATTAAATTAAAGTATTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35636
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 |
|---|---|---|---|---|---|
| ENSDART00000038847 | Nonsense | 108 | 237 | 5 | 9 |
| ENSDART00000102647 | Nonsense | 108 | 237 | 3 | 6 |
| ENSDART00000148210 | Nonsense | 108 | 237 | 5 | 8 |
The following transcripts of ENSDARG00000024090 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 14 (position 8455780)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 14 | 8179024 |
| GRCz11 | 14 | 8485138 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTCCAGACAGGATTATGACCTCAGGCTGAGGTACCAGTATGCTGGAGGT[C/T]AGGCCTTCAGAACCTCCTCCAGCTCCTCCAACAATCCCAGGTGAGAAACA
Long Flanking Sequence:
TATATATTAGACCATACTCCTGATACCTCAGATGTATCTGTGTATTATTATATTTTATTTTACATGTGTAAATATAATTGAAACAAGAAAAATACTGTAAAATATTAAACATTTTAAATACTAAATATAGATTACATTTTGTAGTCTTTTTAATAACTTGTTTAAATTTAAATGCATTATCTTTCTTTTCCTAAAGATGGTACGTGACCAAACTCTATTGAATTGATATAACTGCTTAATAAAATGATTTTGTTTAAATGCACCAAACAATTATTGGCTATATTCACTGAGAACTGGATCTATATAGTGTAATGTGATTGCTTTGATTTGGGAAGAAAGATAAGTTCTGTTTTCTCCTTCAGTTGCACCCAGACAGTGACCCATCCAATCCTGGTCTGCACACACAGTTTGTGCAGCTGAATGAAGCGTACAGGGTGCTGAGCAAAGAAGGGTCCAGACAGGATTATGACCTCAGGCTGAGGTACCAGTATGCTGGAGGT[C/T]AGGCCTTCAGAACCTCCTCCAGCTCCTCCAACAATCCCAGGTGAGAAACAATATTTTTTTTATAATCAACAAGCTTGAATTTAAAGGGTTAGTTCATGCAAAATAATGTTTATTCTCTTATGATTTACTCAACCTCATGTCATTCCAGTGTAATAAATAGGGCCAGGCGGAGTCTGCGGACGTTTCTGCTGAGAATTTTGGTAAAAATCTGCAGATTTCTGCTTAATTATTTTGGGAGTACCATAACTATAACCTTAATATGTGAAATAAAAAAATAATATCTTTTTAACTTTTATTTAATGTTTAAAATGCAAATCCAATTAGATTCACTTTATTTGGTAAACAAAGCAAGTCTCTTATATAATATATTGACTAAAAGACAGAAAATATCCATTTTATTTACCATAGATATTACCAACATCTGGGGACTTACGCGAAAAGATTACGCGAAAAGATTTAGCAACTTTTCAGACCCCCTTAGTGACAAATTTTTTTAAAAA
Associated Phenotype:
Not determined