ZMP
dnajc3
Ensembl ID:
ZFIN ID:
Description:
dnaJ homolog subfamily C member 3 [Source:RefSeq peptide;Acc:NP_955904]
Human Orthologue:
DNAJC3
Human Description:
DnaJ (Hsp40) homolog, subfamily C, member 3 [Source:HGNC Symbol;Acc:9439]
Mouse Orthologue:
Dnajc3
Mouse Description:
DnaJ (Hsp40) homolog, subfamily C, member 3 Gene [Source:MGI Symbol;Acc:MGI:107373]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa16813 | Nonsense | Available for shipment | Available now |
| sa34665 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa16813
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 |
|---|---|---|---|---|---|
| ENSDART00000060246 | Nonsense | 291 | 504 | 8 | 12 |
The following transcripts of ENSDARG00000041110 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 30523363)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 29679309 |
| GRCz11 | 9 | 29490055 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTTGTTTGTTTTYGTAAATGCACAGGTACAGTGATGCAGTCAGTAAATA[C/A]GAGTCTGTTATGAAGACTGAACCGAATGTTCCCCACTTCACACTGAACGC
Long Flanking Sequence:
AATGTGAAATGCAGATTTACAGTTTGATATGACTGACTTTTTAAATATATTTTACAATGTAGTTCACTATAATGGTATAGCTGAATGTTTAATGTTCATCATTGCAACATGATCTATATAATGGGATCATGATATACTGATTCAGTGTTTAGAAATAATTATTTAATTAATATGAGTAATTAGATGTATATTACATTGTAAATGTAGTGCAGAATAGCTTAGTTAAAATTGTAAAAACTTTTTTTAGGGTTTATTTGTGGTAAAAAAAACAACGATGTTTTATGGAGAAAAGTTCTGAAAACAGCATTTATTTGAAAAAAAAAAGAAAAAATAGTATTCCACTAATTTTTGCTAAATAAAAGTAGCCTCGCATTTTTTTTATTTGTGCAGGAAATTTTAAGTATTTGAAGTAAATGTACACCTATTGATCAACTGTCTAAATAATCTAAATGTTGTTTGTTTTCGTAAATGCACAGGTACAGTGATGCAGTCAGTAAATA[C/A]GAGTCTGTTATGAAGACTGAACCGAATGTTCCCCACTTCACACTGAACGCTAAAGAACGCATGTGCCACTGCTTATCAAAGGTGAGGATGAGCTTCTGTCCACAAGATGTCGCTGTCAGCTAAAACATACGCTGCGTCTGTGCTGAATTAACATACTGTAAGTGAACAGGTTTCACTTTTATTTCACAGGACCAGCAAACCGCCAGAGCCATTTCAGTGTGCAGTGAAGTGCTAAACACTGATCCTCAGAATGTCAATGCTCTGAAAGACCGAGCTGAAGCTTTACTGCAGGACGACCAGTATGAAGAAGGTACTGGAAATACTGAACAACACCCACCCAAAACTACACTACAGGGATTTAAAGACATATAGTTATGAAAAATTGAACGATTGCTATTAAATAAAAAATAATATAGACCATTTTGAGGGACGTAAACAAAAACGATGGTCCCAGCCTACTTCCTCCTTCAGATCATCTAAAAAGAGCCACATATTGATCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34665
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000060246 | Nonsense | 484 | 504 | 12 | 12 |
The following transcripts of ENSDARG00000041110 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 30517710)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 29673656 |
| GRCz11 | 9 | 29484402 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGAGAGTCAGCAGGGTGGAGGACATCACCACCACTTCCATGGCGGCTGG[G/T]AAAACTTCCAGGGGTTCAATCCGTTTGGTTCTGGACCTTTTAATTTCAAA
Long Flanking Sequence:
TGTGTAAATATTTTGAACATCTTCTTGGACACTTTTAATGGTTGCAAACAGTTTGCTGCAATTATAAATTGCCCATGTCTTGAGGTAGTTCATTATGAAGCGATTTACCTTCTATGTGCAACTTTGATTGGACAGGAATCACAGGTCTTATTTTTCTAATTCCCGTAGACAAGAAATAATAAAGTAGTGACTGTAGGTAGATGGAAAGTAGTGGAGGTAAAGTACAATACAGCACTAAAAATGTACTCAAGGGAAAGTAAAAGTACACATTTTTAAAACTACTTAGTAAATTACTATTTCTTAGAAAAACTGCTCCATTACAGTAGTTTGAGTATCTGTAATTTGTTACTTTACACTACTGGTTGTTAAGCACCTGTAAACAGTGTCATGCTATTCATTTCTCTACAGAGATGAGGAGTAAGTTTGACCAGGGTGAAGATCCCATGGATCCTGAGAGTCAGCAGGGTGGAGGACATCACCACCACTTCCATGGCGGCTGG[G/T]AAAACTTCCAGGGGTTCAATCCGTTTGGTTCTGGACCTTTTAATTTCAAATTTGGTTTCAACTAAGGCTCTGCTGAAGGACCCGGGGCCTGGATATATGCTGGAGTCAGCAATTGGGAACTTGAGACCCCTCACACACAGGAGCACTTCAGATGGGACAAGCGCCTTGAAGCTCGTGGTCAACTGATCTGTGAACAGCTCCTCTACTACAGGGATCTCACAGTCCTGAGTGCACGGTCAATGTGCGCATCGACCTTTACATTCCTGAGAATCACATGTACATAGAAAACAGTATTTTTCTATGAATCAAACCAAGCTGTAAATAATTAAATAAAGAGATATGAATGCTTATTTAAATTACCTGGGTTTTGGGTCTTTTACTGAAGAGCATAGAGGCATTTAAAGAAATATATCACCCAAAAATGAAAATCCACTTATTTTCTTACACTCAAGTGCTTTTAAACTTCTGTCGAACACAAAACAACAAATTCTGAATCTGAA
Associated Phenotype:
Not determined