ZMP
LOC559762
Ensembl ID:
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 |
---|---|---|---|
sa3227 | Nonsense | F2 line generated | Not yet available |
sa45811 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa16255 | Nonsense | Available for shipment | Available now |
sa7509 | Missense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa3227
Status:
F2 line generated
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 |
---|---|---|---|---|---|
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)
KASP Sequence:
ACGGTCACGATGCGGACGGTGGTGGGGTTGCTCTCTGTGATTATGCTGTA[T/A]GTGCTCCTGAATGATGCTACGGTGGAAAGCACTGCAGAATTTGATCCATA
Long Flanking Sequence:
AAAAAAATCTCCGTTAAACAGAAATTGGGGGGAAAAATAAACAGGTGGGCTAATAATTCACATAACTAAATGTTGCAAACTTCAAGTAAAATTAAATATAATAAACTAAACTATAATAAACTAAACTTAAACTGTTAAACTATAATCTTATCTCAGTAAGATTATAATAACACTGATTTGCAAATCTATTAGATTTAGTTGTATTTATTTTAATTTGTTTAAAAATATTTATTATATTCACATTGATACTTTTGCATATTATTTTTTGGTGGGTAGAACTTATTAATGAAAATGCATGTATTTTTGCTTTTTATGTTGGCTTCAATTGGTCTTTTTCTTTATTTTACAGTATTTAATAATAATTTCCTATTTATTTATTTTGGATTATTTCTTACTCTAGTTTTCCCTTTATAATAATATTACTCTGATAGTCTCGGGGCTGCAGAACACACGGTCACGATGCGGACGGTGGTGGGGTTGCTCTCTGTGATTATGCTGTA[T/A]GTGCTCCTGAATGATGCTACGGTGGAAAGCACTGCAGAATTTGATCCATATAAGGTTTTAGGAGTCACCAGAAGTGCAAGCCAAGCAGAAATCAAGAAAGTCTACAAACGCCTGGCCAAAGAATGGTAAGAATGCTCATCTTTTGTGTACACATTTAAATCAAACCCAAATTGTATACTGTACCATCTTTCATTTTTCCTGCCAGGCATCCTGATAAAAACAAAAATCCTGAAGCAGAAGACATGTTCATCAAGATTACAAAGTCTTATGAGGTATTGCAGCTTATATGTGGCATTTTTACACTGTGTGGTATGGCACAGAACCCCAGAATAGGGTGTTTTTCACTGCATAGGGTAAATTTACATAGTACATTTTCAGTACCACCTCAGCTGTGGTCCCAAGTGAACTGTACCATTACAAAAAAGATACTGATTTGCTAGAGAGAATGATGACTCATGACTACCTTTGTGGGTCATTTTCTATTTATTTGTAGTAGTACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45811
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:
Essential Splice Site
Transcripts:
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)
KASP Sequence:
None
Flanking Sequence:
CAAGCCAAGCAGAAATCAAGAAAGTCTACAAACGCCTGGCCAAAGAATGG[T/A]AAGAATGCTCATCTTTTGTGTACACATTTAAATCAAACCCAAATTGTATA
Long Flanking Sequence:
TAAACTGTTAAACTATAATCTTATCTCAGTAAGATTATAATAACACTGATTTGCAAATCTATTAGATTTAGTTGTATTTATTTTAATTTGTTTAAAAATATTTATTATATTCACATTGATACTTTTGCATATTATTTTTTGGTGGGTAGAACTTATTAATGAAAATGCATGTATTTTTGCTTTTTATGTTGGCTTCAATTGGTCTTTTTCTTTATTTTACAGTATTTAATAATAATTTCCTATTTATTTATTTTGGATTATTTCTTACTCTAGTTTTCCCTTTATAATAATATTACTCTGATAGTCTCGGGGCTGCAGAACACACGGTCACGATGCGGACGGTGGTGGGGTTGCTCTCTGTGATTATGCTGTATGTGCTCCTGAATGATGCTACGGTGGAAAGCACTGCAGAATTTGATCCATATAAGGTTTTAGGAGTCACCAGAAGTGCAAGCCAAGCAGAAATCAAGAAAGTCTACAAACGCCTGGCCAAAGAATGG[T/A]AAGAATGCTCATCTTTTGTGTACACATTTAAATCAAACCCAAATTGTATACTGTACCATCTTTCATTTTTCCTGCCAGGCATCCTGATAAAAACAAAAATCCTGAAGCAGAAGACATGTTCATCAAGATTACAAAGTCTTATGAGGTATTGCAGCTTATATGTGGCATTTTTACACTGTGTGGTATGGCACAGAACCCCAGAATAGGGTGTTTTTCACTGCATAGGGTAAATTTACATAGTACATTTTCAGTACCACCTCAGCTGTGGTCCCAAGTGAACTGTACCATTACAAAAAAGATACTGATTTGCTAGAGAGAATGATGACTCATGACTACCTTTGTGGGTCATTTTCTATTTATTTGTAGTAGTACAGTAAATTGCTGATTATTGTATATCTGATATAATAAATCTATAGAGATCAATGGTAATTGGGCTCCTATGCCCTAAATACCCGTAGTGAATTGTGCTGTAGTGGCACATTTCCAGGCTGTGTCCAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16255
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 |
---|---|---|---|---|---|
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)
KASP Sequence:
ACTCCATCCATCCTTGGTGTCGTCAATGGAAAAGTCTCTTTCTTTCATTA[C/A]GCWGTCGTCAAAGAACACKTGATACAGTTTGTAGATGACTTGCTGCCACA
Long Flanking Sequence:
AAGAAAATGAATGAATGAAGCAAGTTAGTGTGTTTGCAAATGATTGAATAATGCATAACATTGTTTGTTTTTGTATACAATCGAAAAAAAGACATTACTTAAGGGGGCTTATAATATTGACCTTAAAATGGTTTACAAAAAAAAAACTGCTTTAATTCTAGCTGAAATAAAACAAGTAAGACTTTCTCCAGAGGAAAAAATATTATAGGAAATACTGTAAAAAAATCCTTGCTCCGCTAAACATCATTTGGGAAACATTTAAAAAAGATTAAAAAAATAAATAAAATCACAGGAGGGCAAATAATTTTGACTGTATGATCGAGTTATGAGCTAAAATGAGTTTGTGAAGTTGAAATTACAAACGGATTTTTCCCACCTACAGGAATTGGGATTGGTGTGGTTGATGTCGGATACGAGCGACGTTTAGCAAATCACTTGGGCGCACATCAGACTCCATCCATCCTTGGTGTCGTCAATGGAAAAGTCTCTTTCTTTCATTA[C/A]GCTGTCGTCAAAGAACACTTGATACAGTTTGTAGATGACTTGCTGCCACAAAGACTAATTGAAAAGGTTAGTGATCATCATCATGCACTCCTAATAGTGTACTATAAAAACATAATATGTATCACTGAGCAATATAGAGTCCCCATCAATATACTGAGGTGTTAGGACCAACACAGACCACAGATTGAGCGCTCCCTGCTGGCCTCACTAACATCTTTTTCGAACAGCAACCTAGCTTTCCCATGTGTTCTCCCATCATGGTACTCATGGTGCAGCTCTGCTTAGATTCAGTGGGTGACCATGTAAGAGTTGCTGAGAGCTAGCTGTCGGCAAAATGTTAAGTTATTTCACTTTACAGCCATTGAAAATACCCTCAAACATACCTACAAGAAGAAAAAGTTTATATAGCATTTAGAGGTTATTGCATCTGAACTCTTCAAATGCAAATTAAAGGGTGAAGGTCATACAGAACAATTACATTGAGTGTTGAGATATCCCTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7509
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:
Missense
Transcripts:
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)
KASP Sequence:
GTGGTCTTYTGCATGCTACTGTATGYTTCCTCTTCCTCACAGGAGTTTGA[C/T]GCTCCACTTCTCCTTYCTGAATGTGGATAAACACAAAGAATGGATGGCAG
Long Flanking Sequence:
AACAGTCACACTGCTAATGCAATGAAATCATATTTGGAGAGAAAAACAGCTGATGAAACAAAGACAGTTATGAAATGGCCTCCACAGAGTCCAGACCTAAATATTATATACAGTATGTATAGGCAATAGTATAGGCATATGAGATTCACCTGGAGAGAAAAATAAATCATGCTTAATCTAAGGAAGAACTTGATAATAAATAGCACAAAATTTCAAAGAAGACTCAATGACACCAAAGTGCTTGGTGCTAAAGCGGTCACGTTGACAAGACGTTTGATCCTAGTATTTTGATTCCAAAAGTAATTTTGTTCTGAATATTGTGTACATATTTCCCTTATTTTCTGTTTGTATATTAAAGGTATAGTTCACCCTGAATAAGGAACCTGCACTTGCTCAAAACCTTTTAGATAGATAGATTTGTGCAAAAGTCTTAGCCTCCCAAAGCTAGTGGTGGTCTTTTGCATGCTACTGTATGCTTCCTCTTCCTCACAGGAGTTTGA[C/T]GCTCCACTTCTCCTTCCTGAATGTGGATAAACACAAAGAATGGATGGCAGCGGTGCTGGAATTTGCCCAGGACGCCATGCAGATCGACACAGATGAGGATGAAATGGGCACTCGTAAAGTCGACTACACTGGCTATGTCCTAGCGCTCAATGGCCATAAGAAATACCTGTGTCTCTTTAAGCCAGTCTACACGGGAGAAGACTTGGATGGAAAAGCAGAAGAGGAAGGAGGAGTATCGCGATCCAGAAAAAGCACGACACGTTCTCGATCCACATCTCTTCAGATCCACCACAAACTGGACCGACTCGGCCTATGGATGGAGCGGCTGATGGAAGGGACTCTGCCCCGATACTATGTCCCAGCCTGGCCCGGTCTGGATAAGATCACCGTCAATAAATAAAGCCTCGCTGAAGCTAGCTTGCTAATGCTGGAGCTAATACTCAAATTGGTTTAAAAGCACCAAAAGGCCTCGGCGAATGCAGGCTTGTTGCCGCTCGGAG
Associated Phenotype:
Not determined