Busch Lab

ZMP

dnajb11

Ensembl ID:
ENSDARG00000015088
ZFIN ID:
ZDB-GENE-031113-9
Description:
dnaJ homolog subfamily B member 11 [Source:RefSeq peptide;Acc:NP_942116]
Human Orthologue:
DNAJB11
Human Description:
DnaJ (Hsp40) homolog, subfamily B, member 11 [Source:HGNC Symbol;Acc:14889]
Mouse Orthologue:
Dnajb11
Mouse Description:
DnaJ (Hsp40) homolog, subfamily B, member 11 Gene [Source:MGI Symbol;Acc:MGI:1915088]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa41458 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa38747 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa41458
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
ENSDART00000013282 Essential Splice Site 154 360 4 11
ENSDART00000123374 Essential Splice Site 154 360 4 10
Genomic Location (Zv9):
Chromosome 9 (position 33679149)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 32835095
GRCz11 9 32645841
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGACCTTGAAGTAACATTAGAAGAGGTGTATTCAGGGAATTTTGTGGAG[G/A]TGAGCTTCTTGTTTTTCTTGAACTTTCTCCATTTCCATTCTGATGTACTG
Long Flanking Sequence:
ATTCTTACTTTAGTCAGTTCATCATGCATAAAATATAATTTTTTTTTTTTTTTTTGAACGCAGGTACTTTCAGATGAGGAGAAAAGGAAACAGTATGACGCATATGGAGAGGAGGGATTAAAAGAAGGCCATCAAAGTTCACATGGTGATATATTCTCCAGGTAAACAGATCTAAAATATTAAGACCTCTATAAGAAACTGCTGAGATGTTTGTAAATTTTCTCAAACTCTATATCATTAATGAATCACATGATGAATCTAGTTTTAGAAGCATGACTGTTTGAAACAAAAACATTACCACTGCACACTTTTAATTCACAGTATGTGTGGCTGCATTGATGAAATGTTTTTTTTTCCTCCCCTTAAGTTTCTTTGGCGACTTTGGATTTATGTTTGGTGGAAATAGACAGCCAGCTGGCAGAGATATTCCAAGGGGTAATGACATTGTACTGGACCTTGAAGTAACATTAGAAGAGGTGTATTCAGGGAATTTTGTGGAG[G/A]TGAGCTTCTTGTTTTTCTTGAACTTTCTCCATTTCCATTCTGATGTACTGCTGTATTTAGGTAGTCACGTGGAAGTAGATGCTCTTCATAATCTCCTTTCCTTTTTCCTGTCCTTCTGTTTCCTCTCTTTTTCAACATGTAGGTGGTACGAATCAAACCGGTAGCAAAAGAAGCTCCAGGCAAAAGAAAATGCAACTGCCGGCAAGAAATGAGAACAACACAACTCGGACCGGGTCGCTTTCAGATGACACAGGAAGTAGTCTGTGATGAATGCCCCAATATTAAGTGAGTTTTCAAAGTAGCCTTTGTCACTTTGGTTTTATTTTCATATGGTATTTATTAATTTTAAAGTGATCTGGTCATAAATGGTCAACAAAGATGCAATACTGTTTCCACCTTGTTTGGTTTGACTACTTGTGTTAGATTTTTCTACAAGGCCATTTCTTATTTTATGTTTGGTGCAGAGTGTACTTGAATCTACAAATCTATCTTACATGGCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38747
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
ENSDART00000013282 Nonsense 157 360 5 11
ENSDART00000123374 Nonsense 157 360 5 10
Genomic Location (Zv9):
Chromosome 9 (position 33679000)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 32834946
GRCz11 9 32645692
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCTTTTTCCTGTCCTTCTGTTTCCTCTCTTTTTCAACATGTAGGTGGTA[C/T]GAATCAAACCGGTAGCAAAAGAAGCTCCAGGCAAAAGAAAATGCAACTGC
Long Flanking Sequence:
TATATTCTCCAGGTAAACAGATCTAAAATATTAAGACCTCTATAAGAAACTGCTGAGATGTTTGTAAATTTTCTCAAACTCTATATCATTAATGAATCACATGATGAATCTAGTTTTAGAAGCATGACTGTTTGAAACAAAAACATTACCACTGCACACTTTTAATTCACAGTATGTGTGGCTGCATTGATGAAATGTTTTTTTTTCCTCCCCTTAAGTTTCTTTGGCGACTTTGGATTTATGTTTGGTGGAAATAGACAGCCAGCTGGCAGAGATATTCCAAGGGGTAATGACATTGTACTGGACCTTGAAGTAACATTAGAAGAGGTGTATTCAGGGAATTTTGTGGAGGTGAGCTTCTTGTTTTTCTTGAACTTTCTCCATTTCCATTCTGATGTACTGCTGTATTTAGGTAGTCACGTGGAAGTAGATGCTCTTCATAATCTCCTTTCCTTTTTCCTGTCCTTCTGTTTCCTCTCTTTTTCAACATGTAGGTGGTA[C/T]GAATCAAACCGGTAGCAAAAGAAGCTCCAGGCAAAAGAAAATGCAACTGCCGGCAAGAAATGAGAACAACACAACTCGGACCGGGTCGCTTTCAGATGACACAGGAAGTAGTCTGTGATGAATGCCCCAATATTAAGTGAGTTTTCAAAGTAGCCTTTGTCACTTTGGTTTTATTTTCATATGGTATTTATTAATTTTAAAGTGATCTGGTCATAAATGGTCAACAAAGATGCAATACTGTTTCCACCTTGTTTGGTTTGACTACTTGTGTTAGATTTTTCTACAAGGCCATTTCTTATTTTATGTTTGGTGCAGAGTGTACTTGAATCTACAAATCTATCTTACATGGCATGTAGAGCTGCATAATTGGGAAAAAAAAAATTAATTATTGTTAAAACTATTAACTTAATTAAAACCCTCACCCGATCTTAATACTACATTTTTAATGATGAGAATTTTTTAGTTATTGAATTATTCATTCAGAAAGACTTTTTAAAAAT
Associated Phenotype:
Not determined