ZMP
dnajb6b
Ensembl ID:
ZFIN ID:
Description:
DnaJ (Hsp40) homolog, subfamily B, member 6b [Source:RefSeq peptide;Acc:NP_956599]
Human Orthologues:
DNAJB6, DNAJB7, DNAJB8
Human Descriptions:
DnaJ (Hsp40) homolog, subfamily B, member 6 [Source:HGNC Symbol;Acc:14888]
DnaJ (Hsp40) homolog, subfamily B, member 7 [Source:HGNC Symbol;Acc:24986]
DnaJ (Hsp40) homolog, subfamily B, member 8 [Source:HGNC Symbol;Acc:23699]
DnaJ (Hsp40) homolog, subfamily B, member 7 [Source:HGNC Symbol;Acc:24986]
DnaJ (Hsp40) homolog, subfamily B, member 8 [Source:HGNC Symbol;Acc:23699]
Mouse Orthologues:
Dnajb3, Dnajb6, Dnajb7, Dnajb8
Mouse Descriptions:
DnaJ (Hsp40) homolog, subfamily B, member 3 Gene [Source:MGI Symbol;Acc:MGI:1306822]
DnaJ (Hsp40) homolog, subfamily B, member 6 Gene [Source:MGI Symbol;Acc:MGI:1344381]
DnaJ (Hsp40) homolog, subfamily B, member 7 Gene [Source:MGI Symbol;Acc:MGI:1914012]
DnaJ (Hsp40) homolog, subfamily B, member 8 Gene [Source:MGI Symbol;Acc:MGI:1922801]
DnaJ (Hsp40) homolog, subfamily B, member 6 Gene [Source:MGI Symbol;Acc:MGI:1344381]
DnaJ (Hsp40) homolog, subfamily B, member 7 Gene [Source:MGI Symbol;Acc:MGI:1914012]
DnaJ (Hsp40) homolog, subfamily B, member 8 Gene [Source:MGI Symbol;Acc:MGI:1922801]
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa17305 | Nonsense | Available for shipment | Available now |
| sa40972 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa38633 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa14449 | Essential Splice Site | Available for shipment | Available now |
| sa34138 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa17305
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 |
|---|---|---|---|---|---|
| ENSDART00000010035 | Nonsense | 24 | 237 | 3 | 8 |
| ENSDART00000127993 | Nonsense | 24 | 311 | 2 | 9 |
Genomic Location (Zv9):
Chromosome 7 (position 41959766)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 40296076 |
| GRCz11 | 7 | 40567093 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AMATTTAAGATGTCTTGCTTTGAAAAAGGTGTGTATGTGCTTTTNCAGGTA[C/A]AGAAAACTTGCACTAAARTGGCATCCAGACAAAAACCCCAATGACAAAGA
Long Flanking Sequence:
TGAATTAGGTAGGCTAAATTGTCCGTGGTGTATGAGTGTGTATGGATGTTTCCCAGAGATGGGTTGCAGCTGGAACGGCATCCTCTGCGTAAGCATATGCTGAATTTGACGGTTCATTCCGCTGTGGCGACCCTGGATTAATTAAGGGACCAAGCCAAAAAGAAAATGAATGAATAAATGAATGAATAAATAAATGAAAATTAAAAATAAATAAAATAATTAATAACCTAAACTTTTTTTGTGTTTGCATTCATTAATCACCCACATATATGCTGTTATTTTTGTAAATAATTTTTTAATGTTCTAGATATACAAATACACACTATATACACTATATATTATCACTTTCATTCTTTTTTGTACATCTTTGATGTACTTTTTAAATTGTGACTATATATTCTGCATATAAATTTATATTCTGCAGGTGCATGTAGTTTTTGTGCCCTTTTCAAATTTAAGATGTCTTGCTTTGAAAAAGGTGTGTATGTGCTTTTCAGGTA[C/A]AGAAAACTTGCACTAAAATGGCATCCAGACAAAAACCCCAATGACAAAGAGGAGGCGGAGAAAAGGTTCAAAGAAATCTCAGAAGCATATGAAGTCCTGTCAGATGGTATTGGATATTTATTTTTTCTATAATTATTTTTAAATGATACACTGTTTTTTTATTATTGAAAGTGAATAATTTCCTCTTATAAATGTTTGTAAAGTGTAAAGAAATCTACCAAAATAACCTGTCAGTGGTTGAATTGCTTGATTTATGACTATTTTAAGGTGTTGAGGTATGACACATGTCCTGGTATTTTGGCTTTTTAAGTCTTTTTCTTAAGCCAGTTACTTTTTTCTGTATTTCTGCAGTAAAAAAAAAAGTTATGTATTTTCATTTGCATGTCTGCATTTTTTTTTTGTACATCTTCCCATTTACCGTTTTATTAAATGTGTAGAGGTATTTTTAGATTTCATTTATTATTTATTATTAAATATTTCATTTTCCTGTGCAAGACTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40972
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 |
|---|---|---|---|---|---|
| ENSDART00000010035 | Nonsense | 54 | 237 | 3 | 8 |
| ENSDART00000127993 | Nonsense | 54 | 311 | 2 | 9 |
Genomic Location (Zv9):
Chromosome 7 (position 41959676)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 40295986 |
| GRCz11 | 7 | 40567003 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATGACAAAGAGGAGGCGGAGAAAAGGTTCAAAGAAATCTCAGAAGCATA[T/A]GAAGTCCTGTCAGATGGTATTGGATATTTATTTTTTCTATAATTATTTTT
Long Flanking Sequence:
AAGCATATGCTGAATTTGACGGTTCATTCCGCTGTGGCGACCCTGGATTAATTAAGGGACCAAGCCAAAAAGAAAATGAATGAATAAATGAATGAATAAATAAATGAAAATTAAAAATAAATAAAATAATTAATAACCTAAACTTTTTTTGTGTTTGCATTCATTAATCACCCACATATATGCTGTTATTTTTGTAAATAATTTTTTAATGTTCTAGATATACAAATACACACTATATACACTATATATTATCACTTTCATTCTTTTTTGTACATCTTTGATGTACTTTTTAAATTGTGACTATATATTCTGCATATAAATTTATATTCTGCAGGTGCATGTAGTTTTTGTGCCCTTTTCAAATTTAAGATGTCTTGCTTTGAAAAAGGTGTGTATGTGCTTTTCAGGTACAGAAAACTTGCACTAAAATGGCATCCAGACAAAAACCCCAATGACAAAGAGGAGGCGGAGAAAAGGTTCAAAGAAATCTCAGAAGCATA[T/A]GAAGTCCTGTCAGATGGTATTGGATATTTATTTTTTCTATAATTATTTTTAAATGATACACTGTTTTTTTATTATTGAAAGTGAATAATTTCCTCTTATAAATGTTTGTAAAGTGTAAAGAAATCTACCAAAATAACCTGTCAGTGGTTGAATTGCTTGATTTATGACTATTTTAAGGTGTTGAGGTATGACACATGTCCTGGTATTTTGGCTTTTTAAGTCTTTTTCTTAAGCCAGTTACTTTTTTCTGTATTTCTGCAGTAAAAAAAAAAGTTATGTATTTTCATTTGCATGTCTGCATTTTTTTTTTGTACATCTTCCCATTTACCGTTTTATTAAATGTGTAGAGGTATTTTTAGATTTCATTTATTATTTATTATTAAATATTTCATTTTCCTGTGCAAGACTTGTTAAAATGCATTGCCACACAGTTATTGTAATCTCAACATGAATAAAAAAAAAGTTGGTGCTTTTGCTTCTGATAGTAAAATATATTTTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38633
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 > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000010035 | Essential Splice Site | 154 | 237 | 6 | 8 |
| ENSDART00000127993 | Essential Splice Site | 154 | 311 | 5 | 9 |
Genomic Location (Zv9):
Chromosome 7 (position 41955312)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 40291622 |
| GRCz11 | 7 | 40562639 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTTCCTGGATTTTCTCCATTTGGTCCGTCCTTTTCTGGATTTGACACAG[G/A]TATGTTAATCTGTGTGCAGCTCAGTGTTTCTCAAACCTTTTCTGTCATTC
Long Flanking Sequence:
CTGAAAAGTTTGTGTTGATATTAAATATTTTAACTGTGATTCGAAATAATTCAGTATTGATCAGTTAAATTGTTAGGGGAAGAAAAACAAACAAAATATATTTTTTAAATCTAGGTTTCACTTGCTTTTTTTAATTAAATTATTATTTTTTTTTATAATTAGGAAAAACTTTTGAAATAAGTCACTCAATGGCTTTATTGAACCTAGAATGCTTTCTGCTGACCCACAGTGAGCCTGAAATGATGTTTTTATTTTAGATGTATTTTATGTTTTTATTTTAAGTGTAAATATCTTTATAATATCCTAATTTTATGACATCTTTTTTCTACTAAGCTCCTAATTTTCTTTCTTTATTTTTTCTTTATTTTTTTAAGCTGATGACACATTTGAAGGTTTCTTTGGTGGGCGCCGTCACAGAGGTATGAGCAGGAGCAGGACAGCAGGTCCATTCTTTCCTGGATTTTCTCCATTTGGTCCGTCCTTTTCTGGATTTGACACAG[G/A]TATGTTAATCTGTGTGCAGCTCAGTGTTTCTCAAACCTTTTCTGTCATTCCCCACTTAAGATGTAGATGAGGGTTCCAAGCCTCACCTGTCCCCGATCACTCATGCTAATAAACTAGAGCTTCAAGTCTTACTGAACTATATAAAAAACCTTTGATAACCTCAAATTCAGAAACATGAAAAGTGTGGACTAGTCTAGTGCTTTGCTTTATTTTCGACACTTTGGAAACTGCATGCAAAAAGAACATTCAAAAAAAGATCATTTTATTAATTATTTTAGTGTCTGCAATGAGCCTGTTGTACACACATTTTCAAAACATGGTTGTAGGCTTACTACCTCTCTCAAGTTTTGCTCAATGTTAATATGATATCTGTATTTTATTTTCAGTGAAGCAACAGCATGGCTTCTTCTTGTTCCATGTCAAATATTGATTCATTGCAAACTTTTATACCCCTTACCACAGTTTTTGTTCTGCTTCAATTACATTCTGACATTAAATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14449
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000010035 | Essential Splice Site | 203 | 237 | 8 | 8 |
| ENSDART00000127993 | Essential Splice Site | 203 | 311 | 7 | 9 |
Genomic Location (Zv9):
Chromosome 7 (position 41953730)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 40290040 |
| GRCz11 | 7 | 40561057 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACTTAAGTTTATTCAATGCAAATCTCACAGGTAACGTTTGTGTCATTGCA[G/A]TATTGTAGAGAACGGTCAAGAGAGAGTGGAGGTAGAGGAGGACGGTCAGC
Long Flanking Sequence:
AGAAACTTAAAGGTTTACAACTGTTTGATGGCATGTAATTTTTGTGTAAATTAACCCTTTAAATATGGCAGAATTTTGACTGTGTGGTCAGTGATTTATGGACATGCAGGTATAGCCATGGGAAAAGTCAACATTTATTGTACAGCTATTAGTGTAATGGAACATGATCATCATTTTTTCTGTAGGGTTTTCTCCGTTCGGCCCAATGGGTGGAGGAAGCTTCAGCTCATTTTCATCGTCTCCATTTGGTGGTGGAGGTGGGATGAGAAACTTCACCTCCATTTCCACATCCACCAAATTCATCAACGGAAAGAGGATCACCACTAAACGGTACAAAAGAACATATTGGAATAGCTTTTAACCGCTTCACACCTTGGTTGCACAATCATTTTAATAACGTTATTCAGTTACACGTCTTATGCAAATTGCTCACTAAGTGTTGCTCATTTGACTTAAGTTTATTCAATGCAAATCTCACAGGTAACGTTTGTGTCATTGCA[G/A]TATTGTAGAGAACGGTCAAGAGAGAGTGGAGGTAGAGGAGGACGGTCAGCTCAAATCTCTCACAGTCAACGGTAAGGAGCAGTTACTCCGACTGGACAGCAAATGAACTGCAGATGAATGTTCGAAGCGGTTAAACCCAAACATTCCTAAGCATAACCAACCTTCCCAACCAGGCTGATGGCTACCAGTGCACCTGCTCTCCACTAGTCAGCAAACCAAGAGTAGGTAACATGAGCGTTTAGATGGTGCTGTTACCCTCAGTGCAGTGAATCGCAGAGGTAAACAGGGTGAAGTCTCATTCCAGCATTTTTTCCTTTCTTTCTTGGGGACCATTTATTCCTTACAAAACCTCAGTTCGAACAAGCACACTCTATTCCCTTTCTGTCAGCTTTTCTTTCATCCATAAGTGCTTGAAACTGGAGCTTAACAGGTTGTGTTTGCTTTCTGCTGTAGAGCCGTTCAACTGTTCATATGTTGAAGTCTTAACCTCTCCATTCTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34138
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 |
|---|---|---|---|---|---|
| ENSDART00000010035 | None | None | 237 | None | 8 |
| ENSDART00000127993 | Nonsense | 252 | 311 | 8 | 9 |
Genomic Location (Zv9):
Chromosome 7 (position 41934382)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 40270692 |
| GRCz11 | 7 | 40541709 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACGGAGACAGAACACTCTCTGTGGTCCTGCCCCACACAACCGATACCTC[C/T]GAAACGTGGCCCAGAACCCTTCAGAAAAGGAGGAGGTGGAGGAGGAGGAT
Long Flanking Sequence:
AGTTTAATTGCACATAAAAGAAAATGTGGTTAGCCTTAATTTTATGGCTGACTCTCATAAGAGTATTAGTAAACTGCTATGTTAGGGTTAGTATAAAATGTTGACATGCACTTGCAGAGTAACTCATTATAGTCAGAATAATGTCTGCTGGGAAGCATCAACATAAAATGTTCACAGATATTAGGCAGGCAGTTTTTTAATACTCTAATGACTGCCAACTGAAGTGGCAATTTGACTTGCAAAGTAGACCATCATCAACAATAAAGTCCTATTGAAACATTCTGGCTAGTATATTCTGAACTGAAGACTAGGCTAAATTAAAATGTGCATTCAAAGCATACACAAATGTGCAAAAGTGAAGTAACGAAAACAGACAATCAACATTTCATGCAAATTCATCTGCGCTGTGTCTGGTCTTGCTCACAGCTATTTCTGATGACTCTGAGGAAAGACGGAGACAGAACACTCTCTGTGGTCCTGCCCCACACAACCGATACCTC[C/T]GAAACGTGGCCCAGAACCCTTCAGAAAAGGAGGAGGTGGAGGAGGAGGATAGAGGCCTGCAGAATCTGGGAATTGCCAAAGGTTTGTGTCCCAGCTGGATGTTATGCCTTTAGGCTTTACAGGCCAGAACCAGAAGAGCAGAGCTTTTTCATGCAGAGCTGATTCATAAAGATATTCAGTTTTGTATTTGTTCAAGGTTGCATCAGTGAGTCAGATATTAAAAGGTAAGATCTGCCAGTATGGTGGAGGTGGCGTCTACATGCTCGTGAAATTTGTTTCAGCAGGCAACTTTTTTGGCTTGCTTCTGACTGCTGGGAAAGTAGTTTAATGGAGAGCTCCGACAAACACATTCTAGTGGAGTTTTTGATTTAAAGTGATTGAATTCCTCCCTTCTGTGTCCTAGAGCCACAGTTTATATCTATTAAACAATTAAAACCAACACAGGTTTATTGAAAATACGTGCTTCAGTCTATTATTGAACACACTTCAACATGCATTTA
Associated Phenotype:
Not determined