ZMP
Q1RLS4_DANRE
Ensembl ID:
Description:
LOC556590 protein [Source:UniProtKB/TrEMBL;Acc:Q1RLS4]
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 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa41763 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa35008 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa13518 | Nonsense | Available for shipment | Available now |
sa5836 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa10882 | Essential Splice Site | Available for shipment | Available now |
sa16709 | Essential Splice Site | Available for shipment | Available now |
sa35007 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa41763
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000085855 | Essential Splice Site | 63 | 789 | 1 | 14 |
Genomic Location (Zv9):
Chromosome 11 (position 3671484)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 3589988 |
GRCz11 | 11 | 3609375 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAAGCCTCACTGAAATCAAGAAAATGTACAAGAAACTGGCAAGAGAATGG[T/G]GAGTAATAAGGCTGAAATCTACCTGTTTTTGAGCCTGTCATTCAGTGTGT
Long Flanking Sequence:
TTACATTTTTTGAGAGGTGCACGTCAGCGACACCGACGGCCACAGCGAAGGGTTATGCATCAGCACCGTAGCTTACGTCGCCGTTTGACGCAGAAGTGTAAATCAGCCTTAAGGCAGGCACTCAAAGATACTTCTGTGTTTAATTACTTATTTATTACCAACCATATATTGGTATATGCACATTTTGATAATATCGATAAATTTCACCACCCTACTTTCAGGATGCATTTATAGTAGAATCAGTTATTTTCTGGAGTGAATAAATGTGACACTTCCCCAATCTCATCTGTTTGTGAAGTCTGTCGCAGTTCATGTATCAGAAGATGGGAGGCTGGAGTGTTTTTGTGAGCTGCTGTGCTTGGGCGATTCTTCTTCTTGCTCTGTTTGGTGATTCATTGGCATCTGCACCCGAGTTTGATCCGTACAGTGTTCTCGGAGTGTCTAAACATGCAAGCCTCACTGAAATCAAGAAAATGTACAAGAAACTGGCAAGAGAATGG[T/G]GAGTAATAAGGCTGAAATCTACCTGTTTTTGAGCCTGTCATTCAGTGTGTTGTTCAGTTTGAATGTTTAGGTGATGTGTGTACAGTATAATTTGTAAAGTAATATTGTCAATGTCATTTATTGTATGTATTATATGAGAGACCTGCTGTAGCTTTAACAAAAAAAATGGTTGTAATTGGATTTGCATAATAAACTTGTATTAAATAAAGTCATTTTATTTGTTAAAGGGACACTTCACCCAAAAAGAAAAATCCTGTCGTCAAGTTTACAAGTTTTAAACCCTTATCATTATGTTAAACACAAAAGAAGGTAGTTTGAAGAATGTTGGAAACCTGTAGCCATTGACTTCTAAAGTATTTGTTTTTCCTACCATAGACGTCAATGGTTACCGGTTTTCAGCTTTTTTCAGGATATTATCTTCTGTGTTCAACAGAATAAAGAAATTCATAAAAGTTTGGAAGCACTCGAGGGTAAATAGTGAGTAAATTTTCATTTTTGCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35008
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000085855 | Nonsense | 136 | 789 | 3 | 14 |
Genomic Location (Zv9):
Chromosome 11 (position 3669158)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 3587662 |
GRCz11 | 11 | 3607049 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGACAGTTTCTACTTCGACGAATCGTTCTTTCACTTCCCTCGGACGAGT[C/T]GAGACTTCACCGAGAGCAAACATCTCCTACACTACAACCAGTACATGAAT
Long Flanking Sequence:
TAGAAATATTCATTTTCAAAATGGGGTGTACTCAACTATTCTGAGCACTGTAAATATAATTTATGGGTGACAAATTCTGTCATTGGCATAAATTGTATTAGCATATTTTATAGTATTAATTAGCCCAGTCAGTAGAGTTTTCTGTAAATGCAGGTAGTTTTTTTTTCAAGAGTTAATATAAACTGACAAAGCAACCAAACAGGGAATTTGAGAGTTTTTTTTTATTTGTTTTTCATTTCAGATGAGCAGATTCTACAACTTTACATGTTTTCCACATTACTCAGAATTGCACTCATTCAAGCGTTTGAAAATAACTTCAATAATAAGCATTCATGATTTATTTCACACAGATTTTATCAAATGAGGAGCGAAGGGCGAACTATGATCGTTTTGGTCAAATGGATGAGAATCAAAACTTTGCGCGGCCGCCGCAGGGCTTCAGACAGTATCATGACAGTTTCTACTTCGACGAATCGTTCTTTCACTTCCCTCGGACGAGT[C/T]GAGACTTCACCGAGAGCAAACATCTCCTACACTACAACCAGTACATGAATGAGGTGCTGCCGGACAGCTTCAAGAGACCCTACCTGATCAAGATCACCTCCGAGTGGTGCTTCACCTGCATTCACATCGAACCCATATGGAAGGACACTGTGCTGGAGCTGGAGCCCTTGGGTAAGTGATTTACGGTGCATACATTTGTTTGGCGTGTTTGTCCCCTCAGCTTGTCGTTTGGGCATATGTGAAACCCGCAATCACTGTCTGATCTGTGCTAAAACAATTGGTCTACACCGCCTGAATTATGGCTCGATTAAAATGAACTCTAGAGCGGTTCGGTTGTAGTACATAGTAGTTAGTCATTGTTTTTCAGTGAATTGAGAGAACACAACTTTATAATATCTGTTTGTGGTTTGAAGGAGTCGGTATCGGTGTGGTGGACATTGGATATGAGAGACAGCTGGCTAACCATCTTGGTGCTCACCGCACGCCATCCATTCTCGGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13518
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000085855 | Nonsense | 239 | 789 | 4 | 14 |
Genomic Location (Zv9):
Chromosome 11 (position 3668606)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 3587110 |
GRCz11 | 11 | 3606497 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGTCAATGGAAAAGTCAYTTTCTTCCACTACTCTGTGGTCAGAGAACACT[T/A]GAGGCAGTTTGTGGAAAGCCTTCTGCCCCAGAGACTAGTAGAGAAGGTAG
Long Flanking Sequence:
AGGTGCTGCCGGACAGCTTCAAGAGACCCTACCTGATCAAGATCACCTCCGAGTGGTGCTTCACCTGCATTCACATCGAACCCATATGGAAGGACACTGTGCTGGAGCTGGAGCCCTTGGGTAAGTGATTTACGGTGCATACATTTGTTTGGCGTGTTTGTCCCCTCAGCTTGTCGTTTGGGCATATGTGAAACCCGCAATCACTGTCTGATCTGTGCTAAAACAATTGGTCTACACCGCCTGAATTATGGCTCGATTAAAATGAACTCTAGAGCGGTTCGGTTGTAGTACATAGTAGTTAGTCATTGTTTTTCAGTGAATTGAGAGAACACAACTTTATAATATCTGTTTGTGGTTTGAAGGAGTCGGTATCGGTGTGGTGGACATTGGATATGAGAGACAGCTGGCTAACCATCTTGGTGCTCACCGCACGCCATCCATTCTCGGTTTAGTCAATGGAAAAGTCACTTTCTTCCACTACTCTGTGGTCAGAGAACACT[T/A]GAGGCAGTTTGTGGAAAGCCTTCTGCCCCAGAGACTAGTAGAGAAGGTAGGAGGACACGTTCTCTTTGTACCTTTTGTTTTTCTCAGACTTTTCTTTCTGTTCCTTTGATTTGCTTTGCTTTTTAATCCGTTTTATTGTTCCTTTTCCTTCTTTTCCATTCTTCTATTTTCTTTCTTCACTCCCTTGTTTTGTTTCCTCATTTTCTTTGCTCTTTTCTCTTTTGATAGGATCTTCCCATTATCATCTTTCATTTAATTTCCAGTTTCCATTTCCTTTACTTCTTTTGCTTTCCTTTTCCTATTTGTTTCGTTTTCTTTTGTTCTTACTCTTTCTTTGCCTTTTCCTTGAATTCCTACCCTCATTTCTTCAGATTTTGTCATTCCCTTCCTTCTTATTTCCCTGTCCTCCACCTCCCCTTTCGTCTTTGTCCCAATTTTTCCTCCTTGATTAGTGTGGCCCTTTTCTTTTCCTTTTCTATTTTCTTTTTTTTTTCTCTACG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa5836
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000085855 | Nonsense | 480 | 789 | 9 | 14 |
Genomic Location (Zv9):
Chromosome 11 (position 3662883)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 3581387 |
GRCz11 | 11 | 3600774 |
KASP Assay ID:
554-3799.1 (used for ordering genotyping assays)
KASP Sequence:
TGACGGGCGGATGGAACGGCAGTGATGATGATAAGCATCGCCTCCATGAG[C/T]AGCTTGAGCTTCTGCAAAGAGACCCCTCCTACCTTACCCATGATGCCATG
Long Flanking Sequence:
CGATTCAATCGAACTAAATAAGGCAGGTGGGAAAGCACCCTTAAGCATCTGCCCTCCCAAAGAGCGCCTCAAACCTCCAAAAGCCATAGCACGTTCATTGCGTTTTGTCTTTATCTTCTGAGGCACAAATCATTAATTATATTAATAAAAGGCCCACATTGGCTTCTCCTACAGCAGCAAATGCCATTTTTCTTTTTGATATTTGGCGCCAGTTTCTCAGGAAGTGACAATTTTTTTCTCCGTGACTCATTGGATTGAAACAGTTCTTAATTTGAAAATGTTTTATGCAATAATCAAATTTTACGCATAAGTCTACGTTACATCTTTGTATGGAACCCGCTACTGTCACCTTGTTTTGTTGCCTCATGAGTTGATTGCTTTTGTGCATGTGACCACAGGTGATTATCTTGGAGAGACGTAGCACTTCAGGACGGGTGTTATATCGGACAGTGACGGGCGGATGGAACGGCAGTGATGATGATAAGCATCGCCTCCATGAG[C/T]AGCTTGAGCTTCTGCAAAGAGACCCCTCCTACCTTACCCATGATGCCATGCTGCCTGAACTTAACAATGAGTTTGCTTCTGTGAGTCTTATAGAGGATACAAGGCATAATTCACTCAAAAATTAATACTATTTTGTTTCTTTTTTTATGTTGAACACAAAAGAAGATATTTTGAAGAATGTAAGAAAGCGGTAACCATTGACTTCCAAGGTAGGAAAAACAAATACTATGAAAGTCAATGATTACAGGTTTCCAGCTTTCTTCCAGATATCTTCTTTTTTGTGTTGGGAGAGTAAACGATGGCTCAATTTTCCGTTTTGGGTAAACTTTTCATTATAATGGAAGTCAGTGGGGCAAAAACAGCCCCAAACATAACGAAAGGGGAGTCAATTTAAACAGTACACAAAGGTTAAAGATATTTACATTGCCTAGAAAGTGCAGAAATACTGAGTTTTTATTGGAAATGATAGTAAAAGAAATGATTACACAATAATAAGGTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10882
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000085855 | Essential Splice Site | 559 | 789 | 11 | 14 |
Genomic Location (Zv9):
Chromosome 11 (position 3660879)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 3579383 |
GRCz11 | 11 | 3598770 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCTCGGCTCTTTTCATCCTGTTCGGGACTGTAATCATTCAGGCCTTCAG[G/A]TTGGASTCACAATTTGGTTAGATTTTTTNCCCAAGCACATTTTTRAGTCCA
Long Flanking Sequence:
CTGCTGTCTGGGCTTTCACTGCTTTTCTACACCTTTCTTCATGTGTTCAATACATTTTCCCTGTGTTATTTCATTTTATTACACATAAATTCATTTGTAAACTAAATAGTTTTGTTTTCTCTGCATATATGGACTTTTTTAATTGTTACCAACATCTGGGGAAAATCAACTGCACCTTTAGAAATATGTTTTCTGAGAAAAATGGCTTGTGCGTTTGTTTTGCGGGCACAATCACAAACACTGTAGTCAAGATCCATCCTTGGATTAATATATTTCATCAGTGACGTGGTTTCAGTGCAGATTTATTTTGCTTAAAAAACAGAACCAATGGAGAATTTAATCTCAAAATTGTTAATGAAATTCATATTTTTAAATAAATGAAACTAAATAAGTTTACATTTGTCATTTGTTTGTCCCAGGCGTGAGATGATGCCTGTTCTGTCGCTGATCTTCTCGGCTCTTTTCATCCTGTTCGGGACTGTAATCATTCAGGCCTTCAG[G/A]TTGGAGTCACAATTTGGTTAGATTTTTTCCCAAGCACATTTTTAAGTCCAGTTGTGCATTTACTTGTATTTGTTATGCTGAACAGTGACTCTGGGGAGGAAAAACCAACCAAACAAAAGGCCACAGAGTCACCAAAGACACCGGAGAGCTCTCCAGGCCCAGAAAGCACTTCAAGGTGAGGCCCGAAAATTTTTTTATTGCACATTGAAATGATATACAGTGGTGTGAAAAAGTGTTTGCCCCCTTACAGATTTATTATTTTTAAGCATGTTTGTCACACTTTAATGTTTCAGATCATCAAACTAATTTTATTATTAGTCAAAAATAACACATCATGCAGTTTTTAAATGAAGGTTATTGTTTTTAAGACAAAAAGCAAACCTACATAGTCTTGAGTCCTTAGTGTGAAAAAGTATTTGCCCCTTGTTAAAACGTAATTCTGGATTGTCACATCTGAGTTCAATTTCTCCAGCAACATCCAGGCCTGATTACTGCCACAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16709
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000085855 | Essential Splice Site | 559 | 789 | 12 | 14 |
Genomic Location (Zv9):
Chromosome 11 (position 3660794)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 3579298 |
GRCz11 | 11 | 3598685 |
KASP Assay ID:
2260-3846.1 (used for ordering genotyping assays)
KASP Sequence:
CACATTTTTRAGTCCAGTTGTGCATTTACTTGTATTTGTTATGCTGAACA[G/A]TGACKCTGGGGAGGAAAAACCAACCAAACAAAAGGCCACAGAGTCACCAA
Long Flanking Sequence:
TAAATTCATTTGTAAACTAAATAGTTTTGTTTTCTCTGCATATATGGACTTTTTTAATTGTTACCAACATCTGGGGAAAATCAACTGCACCTTTAGAAATATGTTTTCTGAGAAAAATGGCTTGTGCGTTTGTTTTGCGGGCACAATCACAAACACTGTAGTCAAGATCCATCCTTGGATTAATATATTTCATCAGTGACGTGGTTTCAGTGCAGATTTATTTTGCTTAAAAAACAGAACCAATGGAGAATTTAATCTCAAAATTGTTAATGAAATTCATATTTTTAAATAAATGAAACTAAATAAGTTTACATTTGTCATTTGTTTGTCCCAGGCGTGAGATGATGCCTGTTCTGTCGCTGATCTTCTCGGCTCTTTTCATCCTGTTCGGGACTGTAATCATTCAGGCCTTCAGGTTGGAGTCACAATTTGGTTAGATTTTTTCCCAAGCACATTTTTAAGTCCAGTTGTGCATTTACTTGTATTTGTTATGCTGAACA[G/A]TGACTCTGGGGAGGAAAAACCAACCAAACAAAAGGCCACAGAGTCACCAAAGACACCGGAGAGCTCTCCAGGCCCAGAAAGCACTTCAAGGTGAGGCCCGAAAATTTTTTTATTGCACATTGAAATGATATACAGTGGTGTGAAAAAGTGTTTGCCCCCTTACAGATTTATTATTTTTAAGCATGTTTGTCACACTTTAATGTTTCAGATCATCAAACTAATTTTATTATTAGTCAAAAATAACACATCATGCAGTTTTTAAATGAAGGTTATTGTTTTTAAGACAAAAAGCAAACCTACATAGTCTTGAGTCCTTAGTGTGAAAAAGTATTTGCCCCTTGTTAAAACGTAATTCTGGATTGTCACATCTGAGTTCAATTTCTCCAGCAACATCCAGGCCTGATTACTGCCACACCTGTTTGCAATCAAGAAATCACTTAAATAGGGCCCTTCTGACAAAGTGAAGTAGACCAAAAGATCCTCAAATGCTAGACATCATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35007
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000085855 | Nonsense | 779 | 789 | 14 | 14 |
Genomic Location (Zv9):
Chromosome 11 (position 3657420)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 3575924 |
GRCz11 | 11 | 3595311 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGGAGCGGCTCATGGAGGGAACTCTACCAAGGCACTACGTTTCAGCCTG[G/A]CCCGGTATGGACACCATCACACCGCAGAAATAAGACTATACCCATAGCAG
Long Flanking Sequence:
ACCTGCCAGTGGGAAAGCACCCTGAACAAAACGAAGGAACTGTTTTGAGCATTTCAAGCCTTTTCTAAAGTCCTACAACTAAATTCACTTCCCGCTTGCAGGTCTCAGAATCTCCACTACTCCTTTCTAAATGTGGACAAGCACCGCCAATGGATGGACTCCCTCATGGAGTCTGCTCCCGACGCCAGGTCGGATGAAGAGGAAGAGGTGGAGGACCCCAGCACCAACAAATTAGACCACACGGGCCACGTCCTGGCGCTCAACGGCCACAAGAAGTACTTCTGCGTATTCAGACCCGTGTTTACAGGTGAGGAAGCTGAACGTAGCAGGTACTCGGATGACGATGCAGCGACCGGAGGAACCAGCAGAACCTCAAGGTCCCGTTCAAGTTCCCGTCAGAAGGCCACGACTCTGGAGATCCACCACAAACTGGACCGACTGGGCCTGTGGATGGAGCGGCTCATGGAGGGAACTCTACCAAGGCACTACGTTTCAGCCTG[G/A]CCCGGTATGGACACCATCACACCGCAGAAATAAGACTATACCCATAGCAGGAGATGTCGAATTCTAGACCTTTTTCAATCTCGATTACATGGTCGTTTTTAAAAGATGTTAAGTTATTTTGTGAAATGCACTGGTTATGAGAGGATATTTAGAGCAGTGTTTCCCAACTCTGTTCCTGAAGGCACACCAACAGTACACACTTCCTAATCAAACACACCTGAATCAACTCATCAGAACATTAGAAAGTCTCCAAAACATGAAGTTAATGAGTCAGATAGGGGAGACGTCCAAAATATGTTGGTGTGCCTTCAGGAACAGGGTTGGGGAAACACTGATTTAGAGCACAATTTGCCTGTTTGCTGCTTTCGAGGTTAAACTCAATTCCCATCTGCCAGTGTAGGCTCGTTTCATTACTGTACGGATGCCGATACCCAGATAAAGCCACTCTGTGTAGCTTTGAATAGGGCTAAATGTGTCTTTACACTGCTGGGGGATTGGCG
Associated Phenotype:
Not determined