ZMP
dnajb12
Ensembl ID:
ZFIN ID:
Description:
dnaJ homolog subfamily B member 12 [Source:RefSeq peptide;Acc:NP_997824]
Human Orthologue:
DNAJB12
Human Description:
DnaJ (Hsp40) homolog, subfamily B, member 12 [Source:HGNC Symbol;Acc:14891]
Mouse Orthologue:
Dnajb12
Mouse Description:
DnaJ (Hsp40) homolog, subfamily B, member 12 Gene [Source:MGI Symbol;Acc:MGI:1931881]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa15775 | Nonsense | Available for shipment | Available now |
sa6308 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa10890 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa15775
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 |
---|---|---|---|---|---|
ENSDART00000057525 | Nonsense | 156 | 371 | 4 | 9 |
ENSDART00000136622 | Nonsense | 50 | 233 | 2 | 6 |
Genomic Location (Zv9):
Chromosome 13 (position 30262516)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 29908464 |
GRCz11 | 13 | 30038914 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACTCATTTGTTTTGTTTTTTTGGACTTCCAAYAGCTATAGGTAATGCGTA[C/A]GCAGTTCTTAGTAACCCTGAAAAAAGAAGGCAGTAWGATGTCTAMGGTGA
Long Flanking Sequence:
CTTTTTGAGATGATTTCGTCGTCATGTGTTTATTAGTCACGTTGAATCAATAAAACTAGTTAAATCTTGTTTTTTCAGCAATCCCTATGGGGATTTCCTGAGTTTTTCTTTGTGATTATCGTTTCTGACTAGTTTTCTACTGATCACACAACCGTGCTTTCCTGACTAGATGTGCATGACAATCACAGCTTCACATTTGCAATTTTATTTCAATTAAGCCATTGACATTCTTGTATTGAAAAAACATAGAATGGAAGTCAATGGCTGCTGTTTCCATTCCTGTTTCTTCAGAATATCATCTTTTTAACCTTAGAATGAATCCCATTATTGTTTAGAACATATGAAAGATAAGTTAATGATGATAAAATGTAAAATTTTGGGTGAACTGTCTCTTTAAACTCATTGTTTCAGTTTGTCAGCAGTCATTACACGTAATTTTGCATGTCATCTACTCATTTGTTTTGTTTTTTTGGACTTCCAACAGCTATAGGTAATGCGTA[C/A]GCAGTTCTTAGTAACCCTGAAAAAAGAAGGCAGTATGATGTCTACGGTGAAGAAAAAGCTCACCCTACTCACAGGCACAGGACCTATCATAGAAATTTCGAGGCAGATATTTCCCCTGAGGATCTGTTCAACATGTTCTTCGGAGGTGGATTTCCAACCAGTAAGTCTTGTGACCTTTTCAAAATGTGGCTTTTGAAGTGCAGTGTGTTAGTGGTTGTGGTCTAATACATTCAGGACCGTTTAATGTGTCATTGTGCCATTTTTGCCTGCGTTTCTAGGTAATGTTCACGTGTATAGCAATGGCAGGATGAGGTTTGGCCATCAACAGCGACACGAACGACAAGAACAACAGAGAGAGGTAAGAGCTCGATTGTCCTGCATGTTTTGGGAGGGGTTTGGACTTATAAGCTTATAACAGTGTGCATTTACTTTAAGATTTTAGCAAATTTATATACATTTAGCATTTAGAAAGTACCGAATGAAGAGATTGATCACCCAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6308
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 |
---|---|---|---|---|---|
ENSDART00000057525 | Nonsense | 168 | 371 | 4 | 9 |
ENSDART00000136622 | Nonsense | 62 | 233 | 2 | 6 |
Genomic Location (Zv9):
Chromosome 13 (position 30262552)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 29908500 |
GRCz11 | 13 | 30038950 |
KASP Assay ID:
554-4783.1 (used for ordering genotyping assays)
KASP Sequence:
ATAGGTAATGCGTACGCAGTTCTTAGTAACCCTGAAAAAAGAAGGCAGTA[T/A]GATGTCTACGGTGAAGAAAAAGCTCAYCCTACTCACAGGCACAGGACCTA
Long Flanking Sequence:
TCACGTTGAATCAATAAAACTAGTTAAATCTTGTTTTTTCAGCAATCCCTATGGGGATTTCCTGAGTTTTTCTTTGTGATTATCGTTTCTGACTAGTTTTCTACTGATCACACAACCGTGCTTTCCTGACTAGATGTGCATGACAATCACAGCTTCACATTTGCAATTTTATTTCAATTAAGCCATTGACATTCTTGTATTGAAAAAACATAGAATGGAAGTCAATGGCTGCTGTTTCCATTCCTGTTTCTTCAGAATATCATCTTTTTAACCTTAGAATGAATCCCATTATTGTTTAGAACATATGAAAGATAAGTTAATGATGATAAAATGTAAAATTTTGGGTGAACTGTCTCTTTAAACTCATTGTTTCAGTTTGTCAGCAGTCATTACACGTAATTTTGCATGTCATCTACTCATTTGTTTTGTTTTTTTGGACTTCCAACAGCTATAGGTAATGCGTACGCAGTTCTTAGTAACCCTGAAAAAAGAAGGCAGTA[T/A]GATGTCTACGGTGAAGAAAAAGCTCACCCTACTCACAGGCACAGGACCTATCATAGAAATTTCGAGGCAGATATTTCCCCTGAGGATCTGTTCAACATGTTCTTCGGAGGTGGATTTCCAACCAGTAAGTCTTGTGACCTTTTCAAAATGTGGCTTTTGAAGTGCAGTGTGTTAGTGGTTGTGGTCTAATACATTCAGGACCGTTTAATGTGTCATTGTGCCATTTTTGCCTGCGTTTCTAGGTAATGTTCACGTGTATAGCAATGGCAGGATGAGGTTTGGCCATCAACAGCGACACGAACGACAAGAACAACAGAGAGAGGTAAGAGCTCGATTGTCCTGCATGTTTTGGGAGGGGTTTGGACTTATAAGCTTATAACAGTGTGCATTTACTTTAAGATTTTAGCAAATTTATATACATTTAGCATTTAGAAAGTACCGAATGAAGAGATTGATCACCCAAATAGTCTGTACGCACCCTTTACTAGTCCAGACCTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10890
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 |
---|---|---|---|---|---|
ENSDART00000057525 | Nonsense | 171 | 371 | 4 | 9 |
ENSDART00000136622 | Nonsense | 65 | 233 | 2 | 6 |
Genomic Location (Zv9):
Chromosome 13 (position 30262561)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 29908509 |
GRCz11 | 13 | 30038959 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCGTACGCAGTTCTTAGTAACCCTGAAAAAAGAAGGCAGTAWGATGTCTA[C/A]GGTGAAGAAAAAGCTCAYCCTACTCACAGGCACAGGACCTATCATAGAAA
Long Flanking Sequence:
ATCAATAAAACTAGTTAAATCTTGTTTTTTCAGCAATCCCTATGGGGATTTCCTGAGTTTTTCTTTGTGATTATCGTTTCTGACTAGTTTTCTACTGATCACACAACCGTGCTTTCCTGACTAGATGTGCATGACAATCACAGCTTCACATTTGCAATTTTATTTCAATTAAGCCATTGACATTCTTGTATTGAAAAAACATAGAATGGAAGTCAATGGCTGCTGTTTCCATTCCTGTTTCTTCAGAATATCATCTTTTTAACCTTAGAATGAATCCCATTATTGTTTAGAACATATGAAAGATAAGTTAATGATGATAAAATGTAAAATTTTGGGTGAACTGTCTCTTTAAACTCATTGTTTCAGTTTGTCAGCAGTCATTACACGTAATTTTGCATGTCATCTACTCATTTGTTTTGTTTTTTTGGACTTCCAACAGCTATAGGTAATGCGTACGCAGTTCTTAGTAACCCTGAAAAAAGAAGGCAGTATGATGTCTA[C/A]GGTGAAGAAAAAGCTCACCCTACTCACAGGCACAGGACCTATCATAGAAATTTCGAGGCAGATATTTCCCCTGAGGATCTGTTCAACATGTTCTTCGGAGGTGGATTTCCAACCAGTAAGTCTTGTGACCTTTTCAAAATGTGGCTTTTGAAGTGCAGTGTGTTAGTGGTTGTGGTCTAATACATTCAGGACCGTTTAATGTGTCATTGTGCCATTTTTGCCTGCGTTTCTAGGTAATGTTCACGTGTATAGCAATGGCAGGATGAGGTTTGGCCATCAACAGCGACACGAACGACAAGAACAACAGAGAGAGGTAAGAGCTCGATTGTCCTGCATGTTTTGGGAGGGGTTTGGACTTATAAGCTTATAACAGTGTGCATTTACTTTAAGATTTTAGCAAATTTATATACATTTAGCATTTAGAAAGTACCGAATGAAGAGATTGATCACCCAAATAGTCTGTACGCACCCTTTACTAGTCCAGACCTTTTTGAGTTTCT
Associated Phenotype:
Not determined