ZMP
dnajc21
Ensembl ID:
ZFIN ID:
Description:
DnaJ homolog subfamily C member 21 [Source:UniProtKB/Swiss-Prot;Acc:Q6PGY5]
Human Orthologue:
DNAJC21
Human Description:
DnaJ (Hsp40) homolog, subfamily C, member 21 [Source:HGNC Symbol;Acc:27030]
Mouse Orthologue:
Dnajc21
Mouse Description:
DnaJ (Hsp40) homolog, subfamily C, member 21 Gene [Source:MGI Symbol;Acc:MGI:1925371]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa37242 | Nonsense | Available for shipment | Available now |
| sa25150 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa37242
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000079674 | Nonsense | 248 | 545 | 5 | 12 |
Genomic Location (Zv9):
Chromosome 21 (position 9124670)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 11096960 |
| GRCz11 | 21 | 11189588 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGAGAAGGCCAAGAAAGTGGAAGAACTGAGGAGAAAACAGAAGCTCAGC[C/T]AGGCCAAGTATGTGAGATTACATTGGTTTGAACTATTTAGTGCATACCAT
Long Flanking Sequence:
ATGGATGTTTTGGAGTGTTTGTCATCGGTGGAGGCTTGCAAGTAGCAGATGAACTCAGCACAAGTGTACAATCCTCCTAAAAACTCTGTCTTTTTGTTAAATGAGTGAAGCCTGAGAAGTCTGTGCTGAAAGTTTGGTTTTACGTGCTTTTATCAATCTCTGGTTTTATTTCTTTAATGTATGATCTTTTTTTTGTCCTTCAGGTGGTGCATTTATTTTATGGCTACTGGCAGAGCTTCTGTACACGGAAGAACTTTGCGTGGAAGGAGGAATACGACACGCGACAGGCCTCCAACCGCTGGGAGAAGAGAGCCATGGAGAAGGAGAACAAGAAAACCAGAGACAAGGCCAGGAAGGAGCACAGCGAGCTGGTGCGGCAACTAGTGGCCTTCGTCCGCAAGCGAGACAAGCGTGTGCAGGCTCATAAGAAGCTGGTGGAGGAGCAGAACGCAGAGAAGGCCAAGAAAGTGGAAGAACTGAGGAGAAAACAGAAGCTCAGC[C/T]AGGCCAAGTATGTGAGATTACATTGGTTTGAACTATTTAGTGCATACCATTGCTAAATACTGCAAAAAGTGTTTGTGTTTATTGCTTGTATATTTAAAACTATCCTGATTTATTGGTTATTTATATATTTATATAAGTTAGACCAGCTTAAAATAATTCTCATAAGTACCTATAACCATTTTAATAACTACTTAATCTGAAATGTGTACATCAGGGTTCCCACGCTTTTTGAAAGTACTTAAAAACAAATAGAGGTCCTTGAAAGTGCTTGAATTGAATTTAAAATTAAATTTGTTTATAGTTTTATTTTAACAATTGTACTCAATTGTCAAAATGGATAAATTAAACATCTAAAATTTAAATCATGATGATGATGATGACGATGAGCCTTTATTTGTCACAACACTGTTACATGCAGTGATATTGGAGTCCTTTGGCCATACACAAACATCATACATTTCAAGGGAACACTGGTCATTTGAGAGGTAGCAAAGAAAAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25150
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000079674 | Nonsense | 255 | 545 | 6 | 12 |
Genomic Location (Zv9):
Chromosome 21 (position 9123583)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 11095873 |
| GRCz11 | 21 | 11188501 |
KASP Assay ID:
554-7399.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATGTATGCTGTATATTTATTGATCATTATGTTAGGCTTGCTGAAGACTA[T/A]CAGGAGCAGAGCTGGACTGCAATGTCTGAGCTGGAGAAGGAGCTGCAGCA
Long Flanking Sequence:
ATATAAACATTTTCAGGATAATGCAAGTTATTAAATTATTTATATAATGCATAAGTCCTTAAAAAATGTAAAGTTGAAAAAGTGAACAAATTATGTAAATTCTATCAGATTAAACCTTTATATATTTAAATGTTCCAGTTTATCTGGAAACGTTTCTGCATTTTATTCATCCATCCATCGTTAATTGTTATTATATAGTAGAATAGTTAGTAGATGGATAAAATGCAGAAGTTAATTCAGATAAACTGAAACGTTTACATGTGTAAAAGTTTATTCGGAAACAATTTCTCTAATTTGTTCACTTTTTCAACATCCATCCATCCATCCAACTGCATTTCCATGATTTATATCTACAGTTAACTATAGATATATGAATAGATAGGTTAAATGCAGAAATTAAATCAGATAAACTGAAACTTTTACATGTATAAAAGTTTAATATCTAAATTGTATGTATGCTGTATATTTATTGATCATTATGTTAGGCTTGCTGAAGACTA[T/A]CAGGAGCAGAGCTGGACTGCAATGTCTGAGCTGGAGAAGGAGCTGCAGCAGATGGAGGCTGAATATGGACAGGAGTTTGGAGACGCCTCCGACAGTGAGGAGAACGAGGAGGAGCTGGAGAGTCGGGACATAGCAAATGTGGATGGCGTTGGTGAGCTCTGATTTCATCAATACACATACAGCAGTGCATTCTGCTTCAAGTCTGCATAAACCGGAAGTTGCTGCGACTTTTTTCAGTATGTTGATGGGCTTCCAACTTAAATTTAATGTTGAGTAGGGGGCGGGGCTTTCCTTTGTTCATCATTCCCTCTAGAAAACCAACGGTAAGAGGGGCGTGGTTAAGAATATTGATTTGCAGTTGCTATGGAAGCCCTAAAGTTGACGTTAACAAAAGGGCTACCACACCATCTTCTTTTTTTCAGATAAAATATTAAAATTTTTACGATAATGCAAGTTATTGAATAATTTTTATCACATATAGACCTTTTTCATGGCTGCTG
Associated Phenotype:
Not determined