LOC559762

Ensembl ID:
ENSDARG00000059699
Human Orthologue:
DNAJC16
Human Description:
DnaJ (Hsp40) homolog, subfamily C, member 16 [Source:HGNC Symbol;Acc:29157]
Mouse Orthologue:
Dnajc16
Mouse Description:
DnaJ (Hsp40) homolog, subfamily C, member 16 Gene [Source:MGI Symbol;Acc:MGI:2442146]

Alleles

There are 4 alleles of this gene:

Allele name Consequence Status Availability Estimate
sa3227 Nonsense F2 line generated During 2018
sa45811 Essential Splice Site Mutation detected in F1 DNA During 2018
sa16255 Nonsense Available for shipment Available now
sa7509 Missense Mutation detected in F1 DNA During 2018

Mutation Details

Allele Name:
sa3227
Current Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2018.
Mutation:
T > A
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000083267 Nonsense 21 781 1 14
Genomic Location (Zv9):
Chromosome 23 (position 37612562)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 37411790
GRCz11 23 37514452
KASP Assay ID:
554-3024.1 (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
ACGGTCACGATGCGGACGGTGGTGGGGTTGCTCTCTGTGATTATGCTGTA[T/A]GTGCTCCTGAATGATGCTACGGTGGAAAGCACTGCAGAATTTGATCCATA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa45811
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2018.
Mutation:
T > A
Consequence:
Essential Splice Site
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000083267 Essential Splice Site 63 781 1 14
Genomic Location (Zv9):
Chromosome 23 (position 37612435)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 37411663
GRCz11 23 37514325
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
CAAGCCAAGCAGAAATCAAGAAAGTCTACAAACGCCTGGCCAAAGAATGG[T/A]AAGAATGCTCATCTTTTGTGTACACATTTAAATCAAACCCAAATTGTATA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16255
Current 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
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000083267 Nonsense 235 781 4 14
Genomic Location (Zv9):
Chromosome 23 (position 37606489)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 37405717
GRCz11 23 37508379
KASP Assay ID:
2261-8132.1 (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
ACTCCATCCATCCTTGGTGTCGTCAATGGAAAAGTCTCTTTCTTTCATTA[C/A]GCWGTCGTCAAAGAACACKTGATACAGTTTGTAGATGACTTGCTGCCACA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa7509
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2018.
Mutation:
C > T
Consequence:
Missense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000083267 Missense 655 781 14 14
Genomic Location (Zv9):
Chromosome 23 (position 37595752)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 37394980
GRCz11 23 37497642
KASP Assay ID:
554-4285.1 (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
GTGGTCTTYTGCATGCTACTGTATGYTTCCTCTTCCTCACAGGAGTTTGA[C/T]GCTCCACTTCTCCTTYCTGAATGTGGATAAACACAAAGAATGGATGGCAG
Associated Phenotype:
Not determined

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