Busch Lab

ZMP

dnajb6b

Ensembl ID:
ENSDARG00000020953
ZFIN ID:
ZDB-GENE-040426-1122
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]
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]

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.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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.
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.
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.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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.
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