ZMP
si:dkey-172j4.3
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vetebrate diacylglycerol kinase, delta 130kDa (DGKD) [Source:UniProtKB/TrEM
Human Orthologue:
DGKH
Human Description:
diacylglycerol kinase, eta [Source:HGNC Symbol;Acc:2854]
Mouse Orthologue:
Dgkh
Mouse Description:
diacylglycerol kinase, eta Gene [Source:MGI Symbol;Acc:MGI:2444188]
Alleles
There are 7 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa11908 | Nonsense | Available for shipment | Available now |
| sa38605 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa31567 | Nonsense | Available for shipment | Available now |
| sa40878 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa18053 | Nonsense | Available for shipment | Available now |
| sa34055 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa11908
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:
A > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000049885 | Nonsense | 153 | 1074 | 4 | 28 |
| ENSDART00000134535 | Nonsense | 93 | 1014 | 3 | 27 |
Genomic Location (Zv9):
Chromosome 7 (position 24850932)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 23412684 |
| GRCz11 | 7 | 23683841 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGAGCAGGAAGGAGATGGAAGACTGGATCAGTGCTTTGAAGTCTGTACAG[A/T]AATGGGAAACATACGAGGTCTGAACCTTCWCTTTTCACCTTTGGAAAATC
Long Flanking Sequence:
TGCAACAGGGGATGGGAACAGGGGATATGGATAAAGTCCGGTGAGGGCGGGCAGCCATCTGGTCCTGCATCCAGGGGGCGCTGGTCACAGACTCGCCCACCTACTTCAGTAGGTGAAAGCTAAGAAGTTTAATCTTACTTCCGTTTCATCTTTGTTTTGGGCTTTAGCATTGTTTCCTAAACAGATGTGATGTGACAACACACGAGTATAGAAATACTGTATTTTCACTTTTGTCTTCTCAGTGCTCATAGGTCATAGAAATTCAGCTTTTTAATCAGTGAAAATCCAGGAATTTGACATTTTCTTTGAGTGGGAACCGTGTAATTAGTTTGTTCACAGTGATTTCTGTCTCATTCATTCCTTGTTTACAAATACCTACTATGACGTATTTTCTATCCTTTGTCCTCTCCCAGGTCATCACTCCATTCCGTAAGCTGATGTTGTGTGCGGAGAGCAGGAAGGAGATGGAAGACTGGATCAGTGCTTTGAAGTCTGTACAG[A/T]AATGGGAAACATACGAGGTCTGAACCTTCACTTTTCACCTTTGGAAAATCATTCAAAGGTTCAGCAACCGTGCTTTGATGCTTGTAATGGCTGCGCATTATACTGTCTGATGTTCAATCACATGGATTTCGCTTAATCTATGTGAAGTGATCAATAAATGAAAGCCACAGGAGTTATTGCTGCAATTGTAGTTGGATTAGGTGATATTGATGTAAATGAGTCACTCTGTGTGAGTCACCCCAACTACGCACAATTTCTACTTGATAAAATATTTCAGAGCTCGACAAATGTATTTATAGTAATAAAATCTCCTTAGAATTATTCATAATATGAATTATCTAACAGGGTTCAACACTAAGCGTTTTTTCTACTGACCCGATTAGGCCAGTGGTTCAGACTTTTTCCTGCCTTGCCAAAATTCTCACTGGCCCCACCAAAAGAAAAGAACTTTATAGCTATTTCTTAGTCACATATTCTCATACATAGCCTCATTGCAGTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38605
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 |
|---|---|---|---|---|---|
| ENSDART00000049885 | Essential Splice Site | 159 | 1074 | 5 | 28 |
| ENSDART00000134535 | Essential Splice Site | 99 | 1014 | 4 | 27 |
Genomic Location (Zv9):
Chromosome 7 (position 24853421)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 23415173 |
| GRCz11 | 7 | 23686330 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGGTTGAATATTTATAGCACACTGATGCTGACACGATTTGTCTGATTCC[A/G]GGCCAGTCAGTTCAACATGGAGCACTTCTCCGGGATGCATAACTGGTACG
Long Flanking Sequence:
AACAAAAAGAGAAACAAATTGTGTTTTCATGATGATTGAAAAATGAAACATTTAGACGAAGCTTGTATAATTGTGTATTTCAGTTCATTCCTGTGATTTTATGCACAGAATTGAGTCACATCTTACATGTGTTTAAGTATGTCATTAACAACTACTTGTTCAGTTTGGTTTCTTACACATGGCATAGATTTTACACATTTCAATTCACCACTGCCTGTGCTACCTGCAGTTTACACAACCTGCATCCCTGAATTCTGGATTAGCTGAAGGAAGTTGTCACTCCCGTATATTACTGTATACAGAACAGAATTAACCACTACAGCTTAACTGAACCAAACTTAGCAACAGCGTTTAGCTTTGGCTTTTATGTGGCCTATAAGCCATCTTGAGGTCCCATTGGAAGTTCACAGAGGAACTCTAGTTGACAGCTACTGGCCTAGATCTCATTAGTGGGTTGAATATTTATAGCACACTGATGCTGACACGATTTGTCTGATTCC[A/G]GGCCAGTCAGTTCAACATGGAGCACTTCTCCGGGATGCATAACTGGTACGCCTGCTCTCATGCCCGGCCCACTTTCTGCAACGTGTGTCGAGAGGCTCTGCCGGGTGTTACCTCTCATGGTCTCTCCTGTGAAGGTAAACATCAACACAGCTTCACAACAACACCATCTCATGTTTCTGCATTTTCTGTCTTTGTTTTTCCTCTCTTTATGAACAGTGTTTGAATTTTTCCCTTGGGTGCAATTTTTTCTTACATGAGATGTTTATTCTGCTCCTAGAACGAACAATGACGTTGTTTGTTTAGAGCGTAATCAATGAGTCATGAATAGGAACATTGCCCTCAGCCTGTCATCACTTTCTGCTGATGATCTGTTTCATTTCATCCCATCTCCCTGTTTGTGTGTGTTAGTGTGTAAGTTCAAAGCCCACAAGCGCTGTGCCGTACGATCCACCAATACCTGTAAATGGACAACTCTGGCATCTATAGGAAATGACATCATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31567
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:
A > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000049885 | Nonsense | 207 | 1074 | 6 | 28 |
| ENSDART00000134535 | Nonsense | 147 | 1014 | 5 | 27 |
Genomic Location (Zv9):
Chromosome 7 (position 24853841)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 23415593 |
| GRCz11 | 7 | 23686750 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTTCATTTCATCCCATCTCCCTGTTTGTGTGTGTTAGTGTGTAAGTTC[A/T]AAGCCCACAAGCGCTGTGCCGTACGATCCACCAATACCTGTAAATGGACA
Long Flanking Sequence:
GTTGACAGCTACTGGCCTAGATCTCATTAGTGGGTTGAATATTTATAGCACACTGATGCTGACACGATTTGTCTGATTCCAGGCCAGTCAGTTCAACATGGAGCACTTCTCCGGGATGCATAACTGGTACGCCTGCTCTCATGCCCGGCCCACTTTCTGCAACGTGTGTCGAGAGGCTCTGCCGGGTGTTACCTCTCATGGTCTCTCCTGTGAAGGTAAACATCAACACAGCTTCACAACAACACCATCTCATGTTTCTGCATTTTCTGTCTTTGTTTTTCCTCTCTTTATGAACAGTGTTTGAATTTTTCCCTTGGGTGCAATTTTTTCTTACATGAGATGTTTATTCTGCTCCTAGAACGAACAATGACGTTGTTTGTTTAGAGCGTAATCAATGAGTCATGAATAGGAACATTGCCCTCAGCCTGTCATCACTTTCTGCTGATGATCTGTTTCATTTCATCCCATCTCCCTGTTTGTGTGTGTTAGTGTGTAAGTTC[A/T]AAGCCCACAAGCGCTGTGCCGTACGATCCACCAATACCTGTAAATGGACAACTCTGGCATCTATAGGAAATGACATCATCGAGGATGAGGATGGAGTAAGTGATTTTTTTTTCAAGTGATTTGTTCTCTTAAAGGGATAGTTCATCTAATATCTTAATATTCAGTCAGCATTTGCTCTCCCTTGTTCCAAGCTTCTTTCTTCTGTTAAACGCAAAGGAGGATGTTTCGAAAAATGTTGTAAAGCAGCAGCCATTGACGTCCATAATATATTCTGTTCCTACTATGGATGTTAGTGACTGCTGGCTTCCAACACACAGTGCTCAGCATACTTGAGTACACCTCATTTTTAAATGAGTATTTGTATCCGTTTCCCAGTAAATATAGGCAATGTATTTTGGTGCATTTAAACAAAATAGATTTATTAAACAAATATATTTATTAAAATAATATTTTAGTCACCAAACAGATTTAGAAATTGAAAGATAATCCAATTAAATTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40878
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 |
|---|---|---|---|---|---|
| ENSDART00000049885 | Nonsense | 246 | 1074 | 7 | 28 |
| ENSDART00000134535 | Nonsense | 186 | 1014 | 6 | 27 |
Genomic Location (Zv9):
Chromosome 7 (position 24855706)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 23417458 |
| GRCz11 | 7 | 23688615 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCTAAATGTGTGTGTCTGTGTGTGCAGGTGTCAATGCCTCACCAGTGGT[T/A]GGAGGGAAACCTGCCGGTCAGCGCTAAGTGTGTGGTGTGCGATCGAAACT
Long Flanking Sequence:
AAATCTGATCTGAGTAAATCAGAATCCATGTGATTTTTTCCTGCTTACACGTACATGAGCCATATCCAATCTGCGCTAGTAAGTTACTTGAACCATGCAATGTAAACGCAGACAAAGTGCCTAGATAAAAAAAAAAAGATGGCAAAATGAGAACTTTTCTGTCATAAATTAGAGTAAAATAAAAATATTTTTTTAAAAATGAAACCCTTTGAACAGATTAAATACAGGAATCCAGAAAAGGGCGCTCTTTTATTATCAGCTGTCAGTCAGCGCCTGCTCTTGTTTTTCCTAGTCATTATGCCTCTGTCATGTGCTGTGTAAATACAGACAGTCGGATACGAGTCACTTTTAAAAGATGATGTAAACAGGTTAGCAAAAAAAATTTAAAACCAGATACAGTCACAAAATCAGAATTGACCATCAAGATCTGTAGTGTAAATGCAGCCTTCAAGCTAAATGTGTGTGTCTGTGTGTGCAGGTGTCAATGCCTCACCAGTGGT[T/A]GGAGGGAAACCTGCCGGTCAGCGCTAAGTGTGTGGTGTGCGATCGAAACTGCGGCAGCGTCCGGCGACTACAGGACTGGCGGTGTCTCTGGTGCAAAGCCATCGTACGTGACTTTCCTGCCCATACTGTAAAACCAACCCACAATACAGTGCATTTCACCCACACCAACAATAATACACAATCACACCCACTTCAGATTCAGTAACCATAACAACCAGATAAACACACCCGGAGTTTACAGTAAAGACTATGACATCATATGGTACTTGTACAGGTGTGTACCTTGTGCAACCAGTGCGTTAGACTGATGAGTGTTCATGAGTAGTCAGTGATGCATTTGTCTGTGTGTGTAGGTGCACAACAGCTGTAAAGAGCAGTTGGGGAAGGTTTGTCCTCTGGGTCAGTGTAAGGTCTCCATCATTCCACCCACTGCACTTAACAGCATCGACTCTGACGGTAAGGGTTGCCCTGGCAACTGCATCAGCTCAGCTTAGTCTCCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18053
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 |
|---|---|---|---|---|---|
| ENSDART00000049885 | Nonsense | 881 | 1074 | 23 | 28 |
| ENSDART00000134535 | Nonsense | 821 | 1014 | 22 | 27 |
Genomic Location (Zv9):
Chromosome 7 (position 24880489)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 23442241 |
| GRCz11 | 7 | 23713398 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCACGCTGAARTCATGGGAGGACAAGCGTAAAGGTGACAGCCGGCCRTCT[C/T]GACCACGACTCAACTCCCAACAGTCTATGGAGTAYCTGACGGAGGAGGAA
Long Flanking Sequence:
CAGTGGTCATGTCTGGTACTGCGACCAAACAAAATCTTACTGAAAGCTCGTTATTTAAGATATCAACTTTAGATTTGGAATATAATTTGTTCACTTTTATAATTTTGGTAAATTTTAGGCTAAATAATGTTTTATAAAATACGTTTTTGCATTATATTAACATACATTTATTGTTTTATTCTTTTTATGAACATAAAGGCACACGTTTGTTTATTTTGGCATTTTAAACTTTTTTCACTTCAACTACAATCTGACATTTTTAAAATTACATCAAGCTTCAGTCTGTGCACCAAAGCATTAAAGACTAGCAGTGAAAATTAGAGGTGACAGTGAAGGGTTTAAGAATTGTTGTCAGGTGGATTAAGCTCTAAAAATGTCTGAACCCATTCTTTAGTGTCAATTCTCTGCAATTGGTTAACCTGGAGTTGTTGTGTCACCAGGCCTTCGAGAGCACGCTGAAATCATGGGAGGACAAGCGTAAAGGTGACAGCCGGCCATCT[C/T]GACCACGACTCAACTCCCAACAGTCTATGGAGTATCTGACGGAGGAGGAATGTGCTCAGGTCCAGCAGCTTGGCTTAGTGGCCGACACGCTCATCAGCAGGTGTGTGTGAATGAAGAGTCTCTGACACCCACACAGAGCAATGTTACACTGCAGTGAAGATCAGTGCATGCATCTGTGAGAAGCTATTTCAGGGTTATTATACAAATGATTATACCTGTTTTACTGCAAACCGCACCCATTACAGTAACTTCTGATTTGTAGAGATGTGACACTTCCTTGTGTTTGTTCACATGTGATTTTCTTTCATAATCACTTTTAAAAGCATGCATCAAAGGCTTTTGCTGAAAAGAACTTGTTTTGTGCTGCTTCTGAATGCATTGTAGGATTCGGGAAGTGGCGAAGACTCATAAGGTGGTGGAGCAGGAACTGGCTCATGCTGTAAATGCCAGCGCTGCTGTCCTGAGTGAAGCATTTCCTTCCAAACCCTCCAGTCCTGAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34055
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 |
|---|---|---|---|---|---|
| ENSDART00000049885 | Nonsense | 887 | 1074 | 23 | 28 |
| ENSDART00000134535 | Nonsense | 827 | 1014 | 22 | 27 |
Genomic Location (Zv9):
Chromosome 7 (position 24880507)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 23442259 |
| GRCz11 | 7 | 23713416 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGACAAGCGTAAAGGTGACAGCCGGCCATCTCGACCACGACTCAACTCC[C/T]AACAGTCTATGGAGTATCTGACGGAGGAGGAATGTGCTCAGGTCCAGCAG
Long Flanking Sequence:
CTGCGACCAAACAAAATCTTACTGAAAGCTCGTTATTTAAGATATCAACTTTAGATTTGGAATATAATTTGTTCACTTTTATAATTTTGGTAAATTTTAGGCTAAATAATGTTTTATAAAATACGTTTTTGCATTATATTAACATACATTTATTGTTTTATTCTTTTTATGAACATAAAGGCACACGTTTGTTTATTTTGGCATTTTAAACTTTTTTCACTTCAACTACAATCTGACATTTTTAAAATTACATCAAGCTTCAGTCTGTGCACCAAAGCATTAAAGACTAGCAGTGAAAATTAGAGGTGACAGTGAAGGGTTTAAGAATTGTTGTCAGGTGGATTAAGCTCTAAAAATGTCTGAACCCATTCTTTAGTGTCAATTCTCTGCAATTGGTTAACCTGGAGTTGTTGTGTCACCAGGCCTTCGAGAGCACGCTGAAATCATGGGAGGACAAGCGTAAAGGTGACAGCCGGCCATCTCGACCACGACTCAACTCC[C/T]AACAGTCTATGGAGTATCTGACGGAGGAGGAATGTGCTCAGGTCCAGCAGCTTGGCTTAGTGGCCGACACGCTCATCAGCAGGTGTGTGTGAATGAAGAGTCTCTGACACCCACACAGAGCAATGTTACACTGCAGTGAAGATCAGTGCATGCATCTGTGAGAAGCTATTTCAGGGTTATTATACAAATGATTATACCTGTTTTACTGCAAACCGCACCCATTACAGTAACTTCTGATTTGTAGAGATGTGACACTTCCTTGTGTTTGTTCACATGTGATTTTCTTTCATAATCACTTTTAAAAGCATGCATCAAAGGCTTTTGCTGAAAAGAACTTGTTTTGTGCTGCTTCTGAATGCATTGTAGGATTCGGGAAGTGGCGAAGACTCATAAGGTGGTGGAGCAGGAACTGGCTCATGCTGTAAATGCCAGCGCTGCTGTCCTGAGTGAAGCATTTCCTTCCAAACCCTCCAGTCCTGAGGTGACACTAACACTGACTT
Associated Phenotype:
Not determined