ZMP
LOC796987
Ensembl ID:
Human Orthologue:
DPY19L3
Human Description:
dpy-19-like 3 (C. elegans) [Source:HGNC Symbol;Acc:27120]
Mouse Orthologue:
Dpy19l3
Mouse Description:
dpy-19-like 3 (C. elegans) Gene [Source:MGI Symbol;Acc:MGI:2443952]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa40990 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa45293 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa34164 | Splice Site, Nonsense | Mutation detected in F1 DNA | Not yet available |
sa14617 | Nonsense | Available for shipment | Available now |
sa31590 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa40990
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000114669 | Essential Splice Site | 109 | 725 | 3 | 18 |
Genomic Location (Zv9):
Chromosome 7 (position 48765309)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 47032928 |
GRCz11 | 7 | 47306007 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTATTACTCCTACTACAAACAGATGCTGAAGGCCCCTACTATACAGCAAG[G/A]TACTGAGATTTACTCTCAAGACATATTGACTAGTTTTATGATCAATCCTG
Long Flanking Sequence:
AATACACAAAAACACCTGTCAGTAAATTTTATTTTATGAATGAAAGCTCTTGCTATAACTCTTGTGACATGGGATTTTAAAATGTGCTGTTTTTATTAGAACTAAACTATAAGTGAAACTCGTCTCTTAAAACTGCATTTTTGTTGTTGCATATCAACTTTTTGGTCTGGATTGAGTTTAGTTCTGAAAACTGCTTCCACTATAAAACCCAGCATATTTACAACACCTGTTTTCTTTTCTTTCTCAAGACTTTTATTGCGTATGAAATCTGTTTATTCTGTTCCAATATCTGCTCTGATTTCTCTCTCAGATGGGAAATGTATTTCATTTTAACACCATTTACCCATGTTGTGCTTCTTGTCATAGTTCATTTCTAACTGAATCTTATCCTCTCTTCCTGCATTGGTAGGAAGTGGAGCGTGAAATCTCTTTCCGGACAGAATGTGGCCTTTATTACTCCTACTACAAACAGATGCTGAAGGCCCCTACTATACAGCAAG[G/A]TACTGAGATTTACTCTCAAGACATATTGACTAGTTTTATGATCAATCCTGCGTCATGTCATCTTACTGATCACTGATGTTGAAGTCCTTGGCTTTTATTTTTAAGTTGAAATATTGCTCCTGTACTGTCAGGGAAGAAAAAAAGCACCTTCAGGCGTACATCAGTTTATCATTGGGCAAGCATCCTAAAAAGTACAACTTGGTACTTTTTCTACACCACAAAATGTGCAATTTTGTACATTAGTAGTAGTAAATGTACCCCTCAGGTGCTACTGTGAGCTTCTCTGAGTAAATAATGTACAAATATAATGTTATTTTAATGGTACTTCCCCACTTATAAGCTGTTACACCAATAAAAGTACAATCTGCACATTTATTTCTGAGAGTGTAGAGGGCGATTCTTATTTAATTGTAATTTATGTATACAACATGTTCATATATCTAAGATCCAATTTTTGTTTTTCCCTATTCATATATTAAGCTTGGTACATAACGGCAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45293
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000114669 | Nonsense | 419 | 725 | 11 | 18 |
Genomic Location (Zv9):
Chromosome 7 (position 48776658)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 47044277 |
GRCz11 | 7 | 47317356 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGTTGCCATTGGATACATTCGAGCGGTTGGCTGGCACGGTGCTGCTCTA[T/A]CCGTATCTCTGCACCCTCAGTGTGCTCTTCATCTTACTGCTGCTGGTGGC
Long Flanking Sequence:
GTGATTTCATCCTTCACTCTCTCCTTTTTAATTGACAGAAAGTACTCCAGCTCAAATCTGACGAGCACATCTTCAAGTTCATAAAGGCCAAGTTTGGCTTCGGGGCAACGAGGTAAGTCTTTGGTCATCTCTCAGGGCGCTACATCTAAGCCTTTTATCATCAGTCAAATGCCATATCGTGGTGTCTTATTCAGAAGTGAGATCTGCTCGGAGACTGGAGCAAGCCATTAATCCACTGTGATTAAATGCGTCCAGCTCTGGTGGAAAAATAACATCTGGCACGCAACGTAATCTGCTCATCCGCTAGATATTTATGGAGCCATTTGAGTTGATCAGATGAATTGCTGCTCCCAATAATCTGTATAATATATATCCAAGCGCACTCCCTCCCTGCCTCTTTCTTTCAGAGACTTTGATGCCAGTCTCTATCTGTGCGAAGAGGCATTTGGCTTGTTGCCATTGGATACATTCGAGCGGTTGGCTGGCACGGTGCTGCTCTA[T/A]CCGTATCTCTGCACCCTCAGTGTGCTCTTCATCTTACTGCTGCTGGTGGCACTCTCTAATCTCAGGTAAAAGTACTGCATCGCTTCCCTCTCTGCGAGAAACCGCTCAAGTGCAATGCCTCGCCGTATGCTGCGCATTAACCAGATATGTTTTTGCAAATTTAAATATTCTCCTAATGTTCCGTTTACTAATTAGAGTGCAGCAATAGGGTGAGAAATGACCAGAAGAGCCGCGATTATAGCTTCATAACCACCCCGTCCACCACAGGTCACGATGCTAATTTATAATTAGAGTTATTAGTCTTTATTAGATGCGCTACATAATAGATGTGGTTTTTTTTTTCCATTAGGGCTTTTGAATGTGTTATTATGCTTAGTTCAAAGCTGATTTGTTGTTGCTTTAAGGGTTGCAGTGGCCCTCTTTTTGTTCTCTTCCCTTATCAGAATCAAATGAGCCCACAAAAACCCAGAGGCGAGCTCACACTCACATGCACGCACACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34164
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:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000114669 | Splice Site, Nonsense | 610 | 725 | 16 | 18 |
Genomic Location (Zv9):
Chromosome 7 (position 48817791)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 47085410 |
GRCz11 | 7 | 47358489 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGACAAACCATCCACACTACGAGGACCAGGCGCTCAGGGAGAGGACCAGA[C/T]AGGTAAGAGGCTCAGATTTGTTTTCACAATCAGTAAGTTTGCTTGAATCA
Long Flanking Sequence:
GATGACCTCTGAAACATCCATCTTGCTATTCAAATAACATACAGCTTCAGCACTTTCCTGCATGCATCCTATGCACATATATAACATGACAGGAGATGGATCGCATCCAAAGAGAGTGCCTTTTAAACCTGCCGCAGACTACAAACCTTCTGCATTTCAGACATTGGTGATGGGAGTGTACAAATGACTGCATCTGTCCTCACTCAACCATTTCACATTTCCCCCGTTCACCTGAAATAAATGTCTGCAGATTTAGCTTTTCTCATAAATGCCACCACCAGACATCCAGGCCTCTTGTGCAATCCCCTGTCCTGAAATATTAGCGAAGGGAATGTAACAGAGCTCTCTAGTGTTTATTTTGTCTGGACAGATTGAAGACACCCAAACGGGCAGTGTTTGCAGGCAGCATGCAGCTGTTGGCAGGAATTAAGCTGTGTACGGGGAGAGTATTGACAAACCATCCACACTACGAGGACCAGGCGCTCAGGGAGAGGACCAGA[C/T]AGGTAAGAGGCTCAGATTTGTTTTCACAATCAGTAAGTTTGCTTGAATCACAATTCAGTCTTAGCTGGATGTCCAGGACTTTCAGGTCTCGTGGGACAACAGACTCACTTTTTTGGTGAAAAGTTTATTCAAGTCCAAGTAAAAAAATAGTTTGGAAGATACAAGAAATAGTGTTGGGAAAATTACTTCAAATTAGGTAAGGAATTACTAATTGCTAATTACATCATTACAATTTTATTTAAGTTACCTTTGTAATTACTTTGCCTGAAACGTAATTTAATGATAATAATAAAAATAAATAATAATAATAATAATAATAATAATGATTCCTTACGTTTATATAGTGCTTTACTGGACACTCAAATCGCGTCTCTCTTCATCCACCGCCAGTGTGCAGCACCCACCTGGATTACGCGACATCAGCCATATTGTACCAGACACACACCAGCTGATTGGTGGAGAGGAGACAAAGTGATGAAGCTAGTTATGATATGGGGATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14617
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 |
---|---|---|---|---|---|
ENSDART00000114669 | Nonsense | 634 | 725 | 17 | 18 |
Genomic Location (Zv9):
Chromosome 7 (position 48868738)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 47136357 |
GRCz11 | 7 | 47409436 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGTCTGCCGAGGAGGTTCATAAAGTGCTGGGTTCGGYTGGAACAGACTA[C/A]ATTGTGCTGGAGGACAGCATCTGCTATGAGCGCAGGCACAGCCGTGGCTG
Long Flanking Sequence:
AGCAACGTTTACATATTTATAACCACCTAAGAGGAATTTGGGGCTCGTGAGTCACTGGCATTGTGATTTTAGGGATCATGGGCTGAAAATTTTGGGAAAACCTAACCTAAGATATCAAAATGATGCCATTATATTCAGATAAGTAGATACAACTTCTCAATAAAAAAGTTGTTATAAATTCCATGAATCATTGAATAATTATTTCCTCTTTTTTGTAAATGCTTGATGCTTTTCTCATTTAACACAATAATGACTTTACATTTTTTTATTGCTAATTTCTCAGACCATTTAATATGCAACTAATTTGAGATTAATAACATTAATGGCTACATTGTGTAATTAATTAGATGAAAACGTCTAATCAATGACAGCCCTATATGCAGATGTGTGCATGTATTTTTTTTAAATAATGTATTTGTTTTCCTGCAGGTTTATCAGATATATGCACGGCAGTCTGCCGAGGAGGTTCATAAAGTGCTGGGTTCGGTTGGAACAGACTA[C/A]ATTGTGCTGGAGGACAGCATCTGCTATGAGCGCAGGCACAGCCGTGGCTGTAGGCTGAGGGACCTGCTCGACCTGGCAAACGGACATGTAGGTCACACACAGCAGCTCCAGTTCATGCCCACACACACACACACACACACACACACACACACACACACACACATAGTCAGTTAAACTTTTGCATCAAAAACCAAAGAAGAGTTTCAGAGCAGCTGAAATGAACAACTTTGCCCTTTACTGCATTCTGCACATGGCTATAAACAAATATCATTTGGATTAGATGCTAAGCTCACTGGTCTTGCTTTATTTCCATCTCCCAAAGCTCAGGTATTTTTATTTCTTACATTAAATGTCTATAAACGGTTTGTGTAAAGTTGACGCTAACATTTTTCATTTTGTCACATAATCTTGTTCTCACTCACCCACAGCTCATAGTTATTAAATACCGCTCCACCCTGAGCACAATCTACCTTGAGTGACTTTTTTTCCTCTCTGGTAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31590
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 |
---|---|---|---|---|---|
ENSDART00000114669 | Nonsense | 643 | 725 | 17 | 18 |
Genomic Location (Zv9):
Chromosome 7 (position 48868765)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 47136384 |
GRCz11 | 7 | 47409463 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGGGTTCGGTTGGAACAGACTACATTGTGCTGGAGGACAGCATCTGCTA[T/A]GAGCGCAGGCACAGCCGTGGCTGTAGGCTGAGGGACCTGCTCGACCTGGC
Long Flanking Sequence:
TAAGAGGAATTTGGGGCTCGTGAGTCACTGGCATTGTGATTTTAGGGATCATGGGCTGAAAATTTTGGGAAAACCTAACCTAAGATATCAAAATGATGCCATTATATTCAGATAAGTAGATACAACTTCTCAATAAAAAAGTTGTTATAAATTCCATGAATCATTGAATAATTATTTCCTCTTTTTTGTAAATGCTTGATGCTTTTCTCATTTAACACAATAATGACTTTACATTTTTTTATTGCTAATTTCTCAGACCATTTAATATGCAACTAATTTGAGATTAATAACATTAATGGCTACATTGTGTAATTAATTAGATGAAAACGTCTAATCAATGACAGCCCTATATGCAGATGTGTGCATGTATTTTTTTTAAATAATGTATTTGTTTTCCTGCAGGTTTATCAGATATATGCACGGCAGTCTGCCGAGGAGGTTCATAAAGTGCTGGGTTCGGTTGGAACAGACTACATTGTGCTGGAGGACAGCATCTGCTA[T/A]GAGCGCAGGCACAGCCGTGGCTGTAGGCTGAGGGACCTGCTCGACCTGGCAAACGGACATGTAGGTCACACACAGCAGCTCCAGTTCATGCCCACACACACACACACACACACACACACACACACACACACACACATAGTCAGTTAAACTTTTGCATCAAAAACCAAAGAAGAGTTTCAGAGCAGCTGAAATGAACAACTTTGCCCTTTACTGCATTCTGCACATGGCTATAAACAAATATCATTTGGATTAGATGCTAAGCTCACTGGTCTTGCTTTATTTCCATCTCCCAAAGCTCAGGTATTTTTATTTCTTACATTAAATGTCTATAAACGGTTTGTGTAAAGTTGACGCTAACATTTTTCATTTTGTCACATAATCTTGTTCTCACTCACCCACAGCTCATAGTTATTAAATACCGCTCCACCCTGAGCACAATCTACCTTGAGTGACTTTTTTTCCTCTCTGGTAGCTTGATTGTTCTTCTGCTGTTGATTACA
Associated Phenotype:
Not determined