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
sa14449 Essential Splice Site Available for shipment Available now

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:
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