ZMP
DGKZ (2 of 2)
Ensembl ID:
Description:
diacylglycerol kinase, zeta 104kDa [Source:HGNC Symbol;Acc:2857]
Human Orthologue:
DGKZ
Human Description:
diacylglycerol kinase, zeta 104kDa [Source:HGNC Symbol;Acc:2857]
Mouse Orthologue:
Dgkz
Mouse Description:
diacylglycerol kinase zeta Gene [Source:MGI Symbol;Acc:MGI:1278339]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa10033 | Nonsense | Available for shipment | Available now |
sa38004 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa45845 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa24608 | Essential Splice Site | Available for shipment | Available now |
sa38005 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa44233 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa9720 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa10033
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000108625 | Nonsense | 24 | 1107 | 1 | 35 |
Genomic Location (Zv9):
Chromosome 25 (position 8068736)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 7681260 |
GRCz11 | 25 | 7805352 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGCATTTTAAGAGAAAGGAAGCAGGGGACGGTGTGCATGATGACTCCTGT[C/T]GACACCGGAGRCCGAGCATTGCAGTGCCAACCAGCCGTGCCCGACGGCGC
Long Flanking Sequence:
TATATTCACTAACAAAAAGGGGTATACTCAATTATGCTGAGCATATGTACTTATTGATACTTACAATGGTTAAAAAAAAAAGTAAACAGAAAAAAGTTGCATTCATGACATATGTTGCATATGTGAAATCCAAATATGAACTTAGTATTGACTTCCAAAGATCAGATTTCTATATGATGCCTGATGTGACATGTATTATAGATAGATAGAGGTTGTCTCTGTTTGTGATGACATTGAAAAGAACGGGCAAGCGTTGAGTTAGATCATCTCAATTTTAGGGATTAGCTCTAAATCTTGGTCGATGGAGGTCAGTGTGACAAGCTTTCAGTAGTCTTAGAGCGTGGTGTTAAAATCTATGCTGACAGGCTACAATTTTCAACCAACAGCCTCTGGGGGGAACTTTATAAAGAGAGCGCTATCCTCCAGCCACCATGGACACTTTTTTCCGACGGCATTTTAAGAGAAAGGAAGCAGGGGACGGTGTGCATGATGACTCCTGT[C/T]GACACCGGAGACCGAGCATTGCAGTGCCAACCAGCCGTGCCCGACGGCGCTCCAGTGTCGGCCTCCCATCCAGTGCATTAACCCAGCGGCGCCGATCCAGCGTCCAACTTCAGGCATTGCCCCGAATCAACAGCAGTCAACCGGTACATCAAAAGAGCAGCGGTAGACGGAGGTCAAGTACCACCACCCTGAAAGCCAATCCTCGCTTTGCTGTGCGCCGTAAGAAAGTAGGCAAGCTTCGCAATATAGACACACACCTCCTAGGCCCATCCATGCTGCTAGCCAGTCTGATCCAAATGACTCAAGAAGAGGAAGACGATGAAGAAGGTCGCAGTCCGCTCCCAGGGCAAGTGGAGCTCAAGGGAAGCAGCTCGAAGTTCAGGAGTCACACAGATGTGCTGCTTTCTGAAGGTGACAGTGATAGTGATGACTCCAGCGAGCATTCAGAGGAACGTCAATACTCAAGGATACGCAAAGAGTGTCTGGAGGAGGCTGATGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38004
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 |
---|---|---|---|---|---|
ENSDART00000108625 | Essential Splice Site | 258 | 1107 | 5 | 35 |
Genomic Location (Zv9):
Chromosome 25 (position 8078174)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 7690698 |
GRCz11 | 25 | 7814790 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGCTAAAAGTGAACCCAACAAAAAGATATGCAACACCGTGGATTGGACC[G/A]TGAGTTACTCGTCTGTATTTTACCAACAAGTAGGCCTGTCACAATAATCT
Long Flanking Sequence:
TGAAAGCACCTACTATACTGTATGATTTTTGAGCGAGAACAAGAATCTTGTAACATTGATGAGCTAAATAATACAAGCCAAGCATAATGTATACACAGTGTACATAAAGATTAGAAGCAGAAAAACCTACAGATGTCCAAGCCATGCTCTATAGCGCTCTGTGTGGGTTGCTGCTGGTAAAAATAACCGTATTGATTGATACGGAATTAAACAAGTGCAATTTAACAAGACCCCCACCGCTCCAAGGCATTATGAGAAAGCTGCCAACCTTTCAGGGACAAAATAAATGTTCCTAATTTTATTGTTTGTGTGCTGTAATTGACTTAATTAAGATATGATTTGCACATCTGCTTAATATCACTGCCATGTTTTCTTTTTTTTTTTTTCTCAGGAAAGCCATCGCCAAAGCTGGTGTGCAGGATAACGCTGCTCAATCCGGCACAATAACACCTGCTAAAAGTGAACCCAACAAAAAGATATGCAACACCGTGGATTGGACC[G/A]TGAGTTACTCGTCTGTATTTTACCAACAAGTAGGCCTGTCACAATAATCTATGTATCGACTTATCTCACAATGCAAAGACATGACCTCAATCGTTTTGGTGATGCAATACACAGTTGAAGTCAGAATTATTAGCCCCCTTTGAATTTTTTTTTTCTTTTTTAAATATTTCTCAAATTATGTTTAATAGAGCAAGGAAATGTTCACAGTATTTCTGATAATATTTTTTATTTTGGAGAAAGTCTTATTTGTTTTATTTCGGCTAGAATAAAAGCAGTTTTTAATTTTTTAGGAACCATTTTACAGACAAAATTATTAGCCCCTTTAAGCTATATTTTTCGATAGTCTACAGAACAAACCATCATTATACAATAACTTGCCTAATTACCCTAACCTGCCTAGTTAACCTAATTAACCTAGTTAAGCCTTTAAATGTCACTTTAAGCTGTATAGAAGTGTCTTCTATAAAATATCTAGTCAAATATTATTTACTGTCATCATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45845
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 |
---|---|---|---|---|---|
ENSDART00000108625 | Nonsense | 279 | 1107 | 6 | 35 |
Genomic Location (Zv9):
Chromosome 25 (position 8086434)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 7698958 |
GRCz11 | 25 | 7823050 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGGGTCAACACGTGTGGTTTGAGACCAGTCCGGCAGGAGATTTCTGTTA[T/A]GTGGGGGAGTCAAACTGTATCGCAAAGTCCCAGGTAGACACATATTGTAG
Long Flanking Sequence:
GGTTATTTACTTGGGTTTTCATTTTTACTGTCAGATTCCCAAACCAAACAATAATCCCATATCTTAAAATAGACTCTATTGTTGCTTTATAAAAAGTCATCATTATGCTGCTACTCACTCCAAATAATCTTAATAATCATTTGATTTCAATGTACCTACAGAAAGGTATCCGATAAAGCAGTATCCATATAGAGCATTTTGAGGCATGTAAACGATTGTAATGTATTTCCTGTTTTACATTTAGATAGCAAATGAGGATCCAAAGACAGCCACATATTGATAAATAATGTTATGATAGCTGTTTTACGTTATGATTGAATTGCCTTGTTACAGTTATGAATTGGTTTGATAAGCAGGAAATGTTCAAGAGCAAATGACATGACAACATTGAAATGTTCTATAGCAGTAAGCACTCATTAATCTTTTGGTTTTCCACAGGAAAATGCCCAGTTGGGTCAACACGTGTGGTTTGAGACCAGTCCGGCAGGAGATTTCTGTTA[T/A]GTGGGGGAGTCAAACTGTATCGCAAAGTCCCAGGTAGACACATATTGTAGTGATTCTTAAAACAATCATCAGCAAAAATGAGCAGTGTGTATCGAAAAACCCTGCACAACAGCTCCCTCTTCTGGTTAGATGTTCTATATGCATTTAGATAAATCGCTAAGATGCTAATTACCATTTCGTTTTGTCCTCACAGCAAAAGTCTCTTCCCCGCCACAAATGTGCAGCTTGCAAAATATCAGTTCACACAGAGTGCATGAATCAGCTGGACAAGGTTAGAAGTTTGTAGAAACAACTTTTGAACGATTTGGGGTGTAATAACAATGTATCTTCTCAAAGGAAAATGTGCGCTTTCCCTACAGATTAACTTCAGGTGTAAGCCAACTTTTAAAGATCCAGGGACGAAAAATGTCAGAGAAGTAAGACTTTTTGTCATTTTATATCAAGCTTTTTATATATTTCGCTCTGCATAAATGAGTACACCCCCTCACAGGTCCTTTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24608
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000108625 | Essential Splice Site | 610 | 1107 | 17 | 35 |
Genomic Location (Zv9):
Chromosome 25 (position 8097361)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 7709885 |
GRCz11 | 25 | 7833977 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTAATTTAGAGGCCAGCGATGAGGACAAAGATGAACAACAGACCGACAAG[G/T]TGAGCTGACACCAGCAGAGGGCGCAAGACTTTAGCAGAAGAACATCTGCA
Long Flanking Sequence:
CATCTCTGGGAAATGTTTACACATATATATACATAAATGAACACCATTAAACATGTATATATGATGTAAATACAAACTTTTATCCTCGACGCAATTAATCGTAATCAATCTTTGCCCAGCACTAATATAAATATTTATATACACAAATTACTTGTTTGAGCGCACTATTTACTATTATTTTTTTGCATCTTTAGTGTTTTAAATAGTGTTGAATTTTTACAAAGAATGCATGGTAACATCTAACTCGTGTAACTTTATTAAAGACACAAACTAATAATACTGAAGCGATCTTAAAGCTGCAGAACAAGAGAAAAAGAAACCAGTTTTGTTTTCCTGAAAATGTACCTGTTGACATCAAGGGCTACACAGATGAACCAGTATCCAAGATCCTTTCCCATGTTGAAGACGGCATCATCGTCCAGCTGGATCGCTGGAACCTGAGTGTGGAAGCTAATTTAGAGGCCAGCGATGAGGACAAAGATGAACAACAGACCGACAAG[G/T]TGAGCTGACACCAGCAGAGGGCGCAAGACTTTAGCAGAAGAACATCTGCAACAAAGCCAGAGTTTTTAGAAGCTCCTTTATGTTTAGGCCTGTCACGATAATCAGTATATCGACTTATCGGGCAACACATGGACATGACCTCAATCATTTATGGTGGCACAATATATATATATATCTCTCATACATAAAACAATTCAAGCAACATTTTAGCTGATTGTGCAACATCTCTTTTAAGAAAACACTATAGTATTTACTTGAAATTACTATAGTATGTTGTGATGTGGATGCCTTACAACTGAACATAGAGCAGATATCACAGCCTTTGTTATTTTTTACGTTGCACTTTGTTGTTTGCATTTATTATTATTTGTTTAGGATATGCGTTTTCACATTTTGACTCCAATGCCTAATTATTAAATTGTTAAAATAACTATAATTAATTGGAATATTCTTAAAAACAAAATATTGTGTTCTTTGGAAGAGTGAACTTGCATTATGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38005
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:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000108625 | Essential Splice Site | 637 | 1107 | 19 | 35 |
Genomic Location (Zv9):
Chromosome 25 (position 8098693)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 7711217 |
GRCz11 | 25 | 7835309 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGGTTTGTTAAAGGCTTCAGATCTTTTAAGATGCCGTTTTGTTATTTC[A/G]GAGGCTAAACCGGAACGCTTCAACAGTCGACTTCGCAATAAGATGTTTTA
Long Flanking Sequence:
TTCAAATATTTCCCAAATGATGATTAACAGAGCAAAGAAATTTTCACAGTATTTCCTATAATATTTTTTTCTTCTGGAGAAAGTCTTATTTGTTTTATTTTGGCTAGAATAAAAGCAGATTTACATGTTTTTAAAGCCATTTTGAGGTCAATATTATTAGCCCCTTTAAGCTATATTGTTTTTCAATTGTCTACTGAACAAACCTCTGTTATACTATGACTTGCCTAATTACCCTAACCTGCCTAATTAACCTAGTTAAGCCTTTAAATGTCACTTTAAGCTGTATAGAAGTGTCTTGAAAAATATCCAGTAAAATATTATTTACTGTCATAAAATAAATCAGTTATTAGAAATGAGTTATTAAAACTATTATGTTTAGAAATGTGTTAAACAAACATTCTTGCCGTGTAACAGAAATTGGGGAACAAAATACAATTCTGACTTAAAATCTGTGGTTTGTTAAAGGCTTCAGATCTTTTAAGATGCCGTTTTGTTATTTC[A/G]GAGGCTAAACCGGAACGCTTCAACAGTCGACTTCGCAATAAGATGTTTTACGCAGGGGTGAGCATATCTATTAAAGTGCTGTTGACATTTTATGCTACTTGTATCATTTTAAATGTAATGTATATGTTTTAAAACCTATTTCTTTCTACAGACAGCATTCTCAGACTTCCTGATGGGCAGCTCTAAAGATCTGTCCAAACACATCAAGGTTGTGGTAAGTTGAATTTAGTTTTCTTTTGTCTTATTTCTAGTCCAAATATCCTACAAATTCTTAAATCAAGAAGCATTTTCTAGACAAGCAAAACTTATTGTCTTGTTTTATGAAAAAACATGTCAAAATGAAGTTTTTCCTTAAAAGGAGCAAAATAATCTGCCAAATGGGGTAGGCAAAATAATCTTATGTCAAAAAGAAAAACAAGCTTATTTTATTTACCCCATTGGCAGATTATTTTGCTTCTTTTAAGGAAAAAAAACTCACTTAATTTTTGCGTATTATTTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44233
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000108625 | Essential Splice Site | 865 | 1107 | 25 | 35 |
Genomic Location (Zv9):
Chromosome 25 (position 8108108)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 7720632 |
GRCz11 | 25 | 7844724 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAACAGTGATTTGGAGACGTGTCGGCAGCATATCGAGAGGTTGCATGAG[G/T]TGCTTTTCAGCTTGTTGAATGCTTGCGAGAAATGCGCCAGCAGTGAGAAT
Long Flanking Sequence:
CACTTTAGAATGTCCACAATGGTTTCTGTCACCACGACACAAATGGATGCTCTCTAAGATACTCTCTAAGTGCATTAAAGGGGTGATGATTTTGGATACAGCCTTGGTATATTATTTCACTGAAAGACACCGGTCCTCTTAGACCATGTAAGGTGACGCCTGATCTACTTTAAAATGCAGCCCTTACATACATTTTCTTTCTCTTTATTAATGTAGTCAGCAGCCCATCGCAGAGACAGTGCAGATCCAAGTGAACCGTATCAGTATGCATGATTATGAAGCTCTCCATTATGATAAGGAGCAGCTCAAAGAAGCCGGTGAGTATTTCTTCTTCACATCTTCGCTCTTATACACTGATGTACTCTTGCTTTTGAAATACTAGAGACCAGTCCTAACATGTGTGTTCTGTTTTCCTTTCAGCGATTCCCATGGGGATAATTACAGTTCCTGGGAACAGTGATTTGGAGACGTGTCGGCAGCATATCGAGAGGTTGCATGAG[G/T]TGCTTTTCAGCTTGTTGAATGCTTGCGAGAAATGCGCCAGCAGTGAGAATTGGCAGCAACCTCCTTCCTCATTTGTGAAGGTTAAGAGGAGGATCTGAACTATCAAAACGTGGCTCAAAGTCAACATGAATCAAAAACTGACTTTGTTAAAGGGCTAGTCCAGCTAAAAAGTAATGTCTGTTATTAATTAGTCACTAATATGTTGTAATATCCTGAGATCGTTGTTAGATGATATCCAGGAGCTCTCTAAGCCTCTATAGACAGCAAGATGTTGACAAACATTGGCAAAATATTCCATGTATAAAATATTCCGCCACAGTGGAATGAACCCCCAATTATTCCGGCATATGTTTTACACCCATCCACTCATGCATTCACACACACATACACTACAGCTAATTTAGTTTATTTAATTTACTTTTATCGCATGTCTTTGGTCTCTGGGGGAAACCGGAGCCCCCAGAGATAATCCACCTGTATCGTCGCCTTTTCTCCCACAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9720
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000108625 | Nonsense | 897 | 1107 | 27 | 35 |
Genomic Location (Zv9):
Chromosome 25 (position 8113721)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 7726245 |
GRCz11 | 25 | 7850337 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTTTCTCTTTGTTTGTTTGTTTCCCAGGTACAACTGCAGATCGTTTCTAC[C/T]GAATAGATCGTGGTCAGGTACTTTGACRYTTTACATCTCTATTACGCGAC
Long Flanking Sequence:
CATTTCGGTCACGGCCGCCTGCTTTGAGAGCCTTTCTGAATGAATGTGTTTTTCCAACAAGGCAACCCGAGGTGCTGTAATATAATTGGCTAAACTGCGAGGTGGGTTTAAAGAACCAAAACAAAAGACAGCGTTCTGGCACAAAACGCACATTTGTAAAGCAGAATATTGTTTAACGTAACGTTTTTAGTCCGTTGGATTGATATAAGTGGAGATGAATAGAAAAGTTAGTTTGATTTAACAAAAAAATTGAAGGTAGCTAGAATTTACAGTGTAACTAATAATAAAAAATAGGTAACTAGTATATTAAGCTAGTAGTGTTCGTTAATACCATGAATTGTTTACTAAAGTGTTTTCAAAAGTGTGATAATGATGTATAATTAATGTGAAATTGTATCTGAGATTCTTCAGTTTTGACCTTTCCACTAGTTTTAAGTGCCACAAACAAATCTTTCTCTTTGTTTGTTTGTTTCCCAGGTACAACTGCAGATCGTTTCTAC[C/T]GAATAGATCGTGGTCAGGTACTTTGACACTTTACATCTCTATTACGCGACACACTGTGCTGTTTTTTTTTACCCTACAGCATTGCATGTCTCCGCAGGAGCATCTAAACTATGTGTCGGAGATCTCCCAGGATGAGCTTTTCATCTTGGACCCGGAGCTGGTCACCAAGGAGACGGTGGGCACGTCGCCCGGAATGCCGGGGGCGATGGAAACGGTTGTTGGGGGATGTGGATGTTCCAACAGCACAGACCAGTTCGCTTTTCCTGCCTGCTCTCCAGGGCCTTCTCCACTCTGCAGGTAGATTGAAACCAGTCACTTTGGATGACAAAATGTGCAGTTAAACTGGATCAGCTCATGTTGTTAAAGCTGCAAACAGCCTCGAGGTGCAGTTTTATGTCGCTTTTTTTATATCCGCGGATCGTTTTAACACATAGACTAGCACAGTAATGCGTGGGCAGGATGTGCTTCGCCTGTGGGCATGAGATTTCTGAAAATGTCCC
Associated Phenotype:
Not determined