ZMP
NP_001038780.1
Ensembl ID:
Description:
diacylglycerol kinase alpha [Source:RefSeq peptide;Acc:NP_001038780]
Human Orthologue:
DGKA
Human Description:
diacylglycerol kinase, alpha 80kDa [Source:HGNC Symbol;Acc:2849]
Mouse Orthologue:
Dgka
Mouse Description:
diacylglycerol kinase, alpha Gene [Source:MGI Symbol;Acc:MGI:102952]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa17147 | Essential Splice Site | Available for shipment | Available now |
sa29975 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa8725 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa16576 | Nonsense | Available for shipment | Available now |
sa45808 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa17147
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000085642 | Essential Splice Site | 371 | 727 | 13 | 24 |
ENSDART00000134883 | Essential Splice Site | 320 | 676 | 10 | 21 |
ENSDART00000143013 | None | None | 90 | None | 3 |
Genomic Location (Zv9):
Chromosome 23 (position 32488851)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 32323741 |
GRCz11 | 23 | 32250272 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGATGATGACAGTGAGCTCAACACCACACCTGATGGRCAGGTGCTGCGGG[T/C]AGGACTCTGATAYATCTCTACWACTGCATCCACACACKGAAYGATGAGRG
Long Flanking Sequence:
CAGACTAAAAAAGTAAGACCTTCTCCTGAAGAAAAATATAATAGGAAGGAAATACTATGAGAAATGTCCTTGCTCTGTTATAAATAACTCAGGAAATATTTGAAAAAACTATTTATATTTATAATTGATAACATTTTAGCCAGCCTTTAGTATAAATAACCACTGAAAAACGCTATACTAGCCTGCAAAACTCTAAAAAAAAAGCCAAAAAGGCTGTTAAAAAGCTAAATACAAACAACAACATGACTAGTTAGTTAAAAAAAGAAAATACAGCTTTAAATCAGCAAGTTGGTAAAAGAAAACTCAGCTTAAATAGTTAAAAATAATGTATAAACTACAGAAGCAGATCAAATGCAGATAAACTGTGATTTGATCGTCCATTGTACCTACTGTTTTGTGTTCCCTCATCTAGGAAAGGCCGAACTGCATAAAGAACGGCGGCTCATTTCCAGATGATGACAGTGAGCTCAACACCACACCTGATGGGCAGGTGCTGCGGG[T/C]AGGACTCTGATATATCTCTACAACTGCATCCACACACGGAATGATGAGAGTGAAACTAAAGCACAGTCTTCTCTTCTCCAAACAGATCAGCCCCATTCCAGACACTCGTCCTCTTTTGGTGTTTGTCAATCCTAAAAGTGGAGGTAAACAGGGAGAAAGGTGAGAACACGTATATCCATCTAATATATTATGTGTGTTTTTTAGAAGAATAGATTTATTGTCATTGTCACAAGTACAAGTAATTTTAAAAAGTGCTCTCCAGTCAGTGCAACAATCATTTTGTCTATAAAAAATATTAAGTGCTAAAATTACTAAAATAAATTGTAAAAACTACAGATATTTACAATAGAATATGATCAAATATGCTCTAAGACATAACATCTACATAACTACTAAATTACATAAGTAAACTAAACAAATGAAGTCAGTAAATTTGTGTTTTACAGGGTCCTTCGGAAATTTCAGTACTTATTGAATCCTCGGCAGGTTTATAACCTTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa29975
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000085642 | Nonsense | 388 | 727 | 14 | 24 |
ENSDART00000134883 | Nonsense | 337 | 676 | 11 | 21 |
ENSDART00000143013 | None | None | 90 | None | 3 |
Genomic Location (Zv9):
Chromosome 23 (position 32488717)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 32323607 |
GRCz11 | 23 | 32250138 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGATCAGCCCCATTCCAGACACTCGTCCTCTTTTGGTGTTTGTCAATCCT[A/T]AAAGTGGAGGTAAACAGGGAGAAAGGTGAGAACACGTATATCCATCTAAT
Long Flanking Sequence:
TTTAGCCAGCCTTTAGTATAAATAACCACTGAAAAACGCTATACTAGCCTGCAAAACTCTAAAAAAAAAGCCAAAAAGGCTGTTAAAAAGCTAAATACAAACAACAACATGACTAGTTAGTTAAAAAAAGAAAATACAGCTTTAAATCAGCAAGTTGGTAAAAGAAAACTCAGCTTAAATAGTTAAAAATAATGTATAAACTACAGAAGCAGATCAAATGCAGATAAACTGTGATTTGATCGTCCATTGTACCTACTGTTTTGTGTTCCCTCATCTAGGAAAGGCCGAACTGCATAAAGAACGGCGGCTCATTTCCAGATGATGACAGTGAGCTCAACACCACACCTGATGGGCAGGTGCTGCGGGTAGGACTCTGATATATCTCTACAACTGCATCCACACACGGAATGATGAGAGTGAAACTAAAGCACAGTCTTCTCTTCTCCAAACAGATCAGCCCCATTCCAGACACTCGTCCTCTTTTGGTGTTTGTCAATCCT[A/T]AAAGTGGAGGTAAACAGGGAGAAAGGTGAGAACACGTATATCCATCTAATATATTATGTGTGTTTTTTAGAAGAATAGATTTATTGTCATTGTCACAAGTACAAGTAATTTTAAAAAGTGCTCTCCAGTCAGTGCAACAATCATTTTGTCTATAAAAAATATTAAGTGCTAAAATTACTAAAATAAATTGTAAAAACTACAGATATTTACAATAGAATATGATCAAATATGCTCTAAGACATAACATCTACATAACTACTAAATTACATAAGTAAACTAAACAAATGAAGTCAGTAAATTTGTGTTTTACAGGGTCCTTCGGAAATTTCAGTACTTATTGAATCCTCGGCAGGTTTATAACCTTTCCAATGGTGGACCAGGACCAGGGTAAGGATTTTTACTACAATTTTTATATACAGCATATACAAAATTATTAGCCTTCCTGCTTTTTATATGAATTTTTTTTTAATTTTCTAAATATTTCTTAACTGATGTTTAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8725
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 |
---|---|---|---|---|---|
ENSDART00000085642 | Nonsense | 422 | 727 | 16 | 24 |
ENSDART00000134883 | Nonsense | 371 | 676 | 13 | 21 |
ENSDART00000143013 | None | None | 90 | None | 3 |
Genomic Location (Zv9):
Chromosome 23 (position 32487238)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 32322128 |
GRCz11 | 23 | 32248659 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACACTTGAAGGTGGTCATAATCGATTTAATACTCTGTTTTCAAACCAGGT[T/A]GAGTTTCTTCAGAGACGTGCCGAATTACAGAATATTAGTTTGCGGAGGCG
Long Flanking Sequence:
ATGCAGTTTGTAAAATAATATTTTCTGTCTTTTAGGAGATATATTATTATAGATTATTTAATAGTTATTAAAATCTTTTTTCTTTTGAACATCATTTCAATTGACCTAATAATAATTAAATAAAATGCTAATAATTTTGCCTTTAACTGTATAAGCCTGTATTGGCTCAAACGATGGAAAAAGTTCTTCAGTTTACTTGCATATTGTGTGTCAGATAAGCTAAATAAATTGGTGTGCCATACATACCCAGATCCAAAATGACCTGAACATGAAAAGAGTATTGTTTTAGTGGTTACACTGCTTAAAAAAAAGAATTGCAGAAAATCTAAATAAATCGTGTGTATTTTGAGGATAATGCGTGTATAAAGTTTCATTCGCTCACTAAACATTATGCATTATAAAGACAAATTTATGAATATTTTTGGTAATCAGTAAATTATGAGTGCTAAGACACTTGAAGGTGGTCATAATCGATTTAATACTCTGTTTTCAAACCAGGT[T/A]GAGTTTCTTCAGAGACGTGCCGAATTACAGAATATTAGTTTGCGGAGGCGATGGCACAGTGGGGTGGATTCTTGATGCTATAGGTTGGAAACCGACACACATTCACAGCAAATCCATGTGAGCAAGCTTTGCTCTGATTTCACTTTCAACCAACTGCTCTTTTCAATTCCTCAAAGATAAAGCCAATCTGCCGGTGCGCCCTCCGGTGGCTGTGCTTCCTCTGGGAACAGGAAATGATCTTGCACGCTGTCTTCGATGGGGAGGAGGTGAGGACAAAGGCTTCTACCTGTACCTGAAGATTGAACAAATATTTGCATGTAGTTGAGAGCTGCACGGTATTGGAAATTTTGATTTAGTTTTAGTTTCACTGTGTTTTTAATGGTCTCTTTTGCAGGGTTAGTCGGCTATAGTTACATATCAACCAATTCTTATTAGACTATTATTTGTCAAACTGTTTGCTTAATATCTGCAGACCTTAATCCACAGACATTAAACACATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16576
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 |
---|---|---|---|---|---|
ENSDART00000085642 | Nonsense | 522 | 727 | 18 | 24 |
ENSDART00000134883 | Nonsense | 471 | 676 | 15 | 21 |
ENSDART00000143013 | None | None | 90 | None | 3 |
Genomic Location (Zv9):
Chromosome 23 (position 32484923)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 32319813 |
GRCz11 | 23 | 32246344 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATACAGGTGACTCTGGAGGACAGTCAGGAGAGAGGAGACCCTGTGCCCTA[C/A]GAAATCATCAAMAACTATTTCTCCATCGGAGTGGTGAGACTYGTAGAGTA
Long Flanking Sequence:
GTGATCAGCTCCTTTAGAAATATTATTCCCTGGAAAAAACATGAAATGTTCAATACTACAGCACTTTGAACATTCAACAATTAATCTTTATTAAAGCTGGAAACTTTGTGATTTATTGTGCCTAAATGCTTTTCAGTCTAAGGCCCTAAAAACATTCAGGTTATACATTTTCGCTATAGTGATTAAACTTTGCACTGCAGTGCATCCACAAAGCACATTGTGTTCTGAATAGCTGCTCTGGTCAATTATGACTTGAGATTCCTGTGATGTGATTTTTACAGATGCGCACATTACAATGTCAATGCTGAAACAATATACTGGGCAGCCCTAATGTAGTCTGTATGTAGTGTATCTGATGGTTCTGATGTTAAAGGTTATGATGGAATGGATCTGGGCCGGATCCTGAAGGACATCGAGGTCAGTGAGGAGGGGCCGATGGACCGCTGGAGCATACAGGTGACTCTGGAGGACAGTCAGGAGAGAGGAGACCCTGTGCCCTA[C/A]GAAATCATCAACAACTATTTCTCCATCGGAGTGGTGAGACTCGTAGAGTACTTAAATCTTTACAATCTGTTTTAATATAATGGGGTATTTATTTAAGCTGTATGTTAGAGTGGGTTTACGATTCTCACTGTACTGAATGTGTCTTGAACAGGATGCCTCCATTGCTCATCGCTTTCACACAATGAGGGAGAAACATCCACAAAAGTTTAACAGCAGGTAGGTAATGTTTTAGATCAGTGTTTCTCAGCCACATTCCCGGAGGAACACCAGCTCTGTGTATTTTTCTTGTCTCCTTGATCAAACACACCTAATTCAGATCATCAGCTCACTAGCAGAGACAAAGGCTGTTTCTCAATTCCAAGAACACAGAGAACAGACTCGTGATCTCGTGAAGACTGTTCTTGCCAGGTTACCAAAAATCGAACAGAGACAAAAGTACAACCCAATAAACAAAAGTGAATCAAACAAAGTTAGAATAGGAATTCAAAAATATGATCATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45808
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 |
---|---|---|---|---|---|
ENSDART00000085642 | Nonsense | 651 | 727 | 22 | 24 |
ENSDART00000134883 | Nonsense | 600 | 676 | 19 | 21 |
ENSDART00000143013 | None | None | 90 | None | 3 |
Genomic Location (Zv9):
Chromosome 23 (position 32480672)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 32315562 |
GRCz11 | 23 | 32242093 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAAAAACACTTAACCAACTGTCTCTGAACAGATATGAGTGATAAACGAT[T/A]GGAAGTGGTGGGACTGGAAGGAGCCATGGAGATGGGACAGATTTACACCG
Long Flanking Sequence:
CAACTAAAAAGCAAGAGCGCAGTGAGGGCATTAGAGTGATAACACCTGTTACTATTAACCTGCTTCTGGTATTAGAGCTCAAACCGAGCCCATTTCAATCTACCAGATCAGGGACATTCATTCACAAAATGAAGTTCATTACTTAAAAATAAGCGCTTTGTTCAGCCTGAAATAATTGAAAAGCACAACAGGACTGACCTCTGCAACTCTCTCTGGCCTAATGCAGTGTTGTGGGACTCAGCTGGATCTGAGTAGTCTTTCTCTGGAGGGCATCGCCATCCTCAACATTCCCAGCATGCACGGCGGCTCCAACCTCTGGGGTGAGGCAAAAAAAAGTGACCGAATGGACCAAAAGTTGCCCGAGGTCATAGTAGATCCTGAAATCTTAAAAGTGAGCCCACAAGGTAGGTTTCTTTCCATGTGGAGACAAAGTTTTAATATAAAAGTTATCCAAAAACACTTAACCAACTGTCTCTGAACAGATATGAGTGATAAACGAT[T/A]GGAAGTGGTGGGACTGGAAGGAGCCATGGAGATGGGACAGATTTACACCGGCTTAAAGAGTGCAGTCAGACTTGCCAAAACATCTCAGATTACCATCAGGTGAGACGATCGCTTGCAAACAAATGGGTGAAAATGACATGCTCGGACATGCCTGTGTGCATTTGCATAGCTGTTCGCATTTTATTCAGAAGGTTAGAATATTCCATTTGCAACCCACTCATTCTTTTGTCATTAAAAAAGGGCGATGGCCTGTTTGTTTTGTCAGAATTCTATGTAATATAATGTTAATACATTATAATTGTATAAATGTAAAATTGAAAAAAAATGTTTATGTATAGGACAAAGAAGCCTTTGCCCATGCAGATTGATGGAGAGCCGTGGATGCAGCCACCTTGTACTGTAAGTGTCCATTATGTACACAATACTGCTTTTTTAAACCATAGAGTGAAGATTTTGATTCATATGTTGTTGTTTTTTTGTTCAGATTCATAAATTAAGCT
Associated Phenotype:
Not determined