ZMP
dgat1b
Ensembl ID:
ZFIN ID:
Description:
diacylglycerol O-acyltransferase homolog 1b [Source:RefSeq peptide;Acc:NP_001002458]
Human Orthologue:
DGAT1
Human Description:
diacylglycerol O-acyltransferase 1 [Source:HGNC Symbol;Acc:2843]
Mouse Orthologue:
Dgat1
Mouse Description:
diacylglycerol O-acyltransferase 1 Gene [Source:MGI Symbol;Acc:MGI:1333825]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa42756 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa2838 | Nonsense | F2 line generated | Not yet available |
| sa39109 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa42756
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000077185 | Essential Splice Site | 343 | 507 | 12 | 17 |
| ENSDART00000147890 | None | None | 78 | None | 3 |
Genomic Location (Zv9):
Chromosome 16 (position 33284235)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 31022750 |
| GRCz11 | 16 | 30980677 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAGGAAATGGACTACACTAGAATGACAGAGCGGCTGCTTAGGCTGGCAG[T/A]AAGTAAAACAAACTTTAGGGTCAATGCATTCTCCTCAGAATAGAAAGTGT
Long Flanking Sequence:
GGAATATATGAGGGTAATTTTTATTTATGAAAGTGCTTCTTGTTAGAGCATTACTTGCAGTTAAAGCTGTTGCAAATTACACATTTAATTCACTCACGCACACACATACACACACACACAAAGAGAGACTTCTCTAAACAGCATCGTTAACATTTTTGTTTAACATTTGCTGAGAAATCAAAATCTGTTCCTCTTGTCTGTTACAGTTGCTTCTCACTCAGTTATTGGTTGGTTTAACGCAGCAGGTGAGCATCACATCAAACTTGGCGTTTTCATGTCTTGGAGACATATTTCATATCTAATGCTCTTTCTGTTGTCTTGCAGTGGATGGTGCCAATCATTCGGAGTTCAATGAAGCCATTGCAGGTGTGTTCATGTGCTTTATCTTCTGTTGTTCAGCGCCTTGAGAATAAGCGCTCCATTTAATTCAGTGAAGCGCTTTTTCATCTTTCAGGAAATGGACTACACTAGAATGACAGAGCGGCTGCTTAGGCTGGCAG[T/A]AAGTAAAACAAACTTTAGGGTCAATGCATTCTCCTCAGAATAGAAAGTGTTTTTGCTTAGATCTGGCATGTTTTGATGGAGGATTTGAAACGAGAATCAAATGATGGAATAATTTTTTTTTACACTAGGTGCCCAATCATCTCCTCTGGCTAATATTCTTCTACTCGTTTTTCCACTCCTCAATGAACTTCATGGCTGAGCTGTTGAGGTTTGGAGATCGGGAGTTTTACCGTGACTGGTGGTGAGTGATTATTATCCCTTTTGAATGAGACTCAATCGAATCGAGTGTGTTTACCTGGTCAATATAAGCAGATGACAATCAAAATTTCAGATTTTTTTAAATAAATTGTTTTTATAATCTTTAAAATTACAGAAATATACTAAAAAAATAAAATAAAATAGCTTTTATGTGAGATTCCAAGCTTAGACAGATTTTGCACCGTCAGCTAACTTCACAACCCAATCATCAGTGTCAAAAATTAAAAAATGTTGAAAGGAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2838
Status:
F2 line generated
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 |
|---|---|---|---|---|---|
| ENSDART00000077185 | Nonsense | 412 | 507 | 15 | 17 |
| ENSDART00000147890 | None | None | 78 | None | 3 |
Genomic Location (Zv9):
Chromosome 16 (position 33282146)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 31020661 |
| GRCz11 | 16 | 30978588 |
KASP Assay ID:
554-2578.1 (used for ordering genotyping assays)
KASP Sequence:
GTGCTTCTCTCTCCTGTTTTCAAAGGCACTTTTACAAGCCGCTGCTGAGA[C/T]GAGGTGCCGGCAAGTTACTGAGCCAATCAGCTGTGTTTTTCGCCTCTGCT
Long Flanking Sequence:
CAACAAAAATCCGGTTTTGATGTTTTTAAAATCTGTTAAACCTCTAGTTAGAGTAAATTACAAGCTAATTTGTTTAGCTGTCTATTCAAAGCATAGGACGGTTGTGACCTCTATTTTACAGTTATTGTTTTTGCATTATTATTAAATGAGCAGCTAGAGGTACCACTTCCCCAACATGCTGCATTTGAAAGGCATAAGTCTCAGATGTATTGTGACCCTGTGTTTGTTTCAGGAACTCTGAAACGATAACGTACTTCTGGCAAAACTGGAATATTCCCGTGCACAAGTGGTGCCTCCGGTGAGTGAACGGCAGGTTTGAAAGCGACAACAGACAGCTGTTGAAATACGACACAGTAAAACCCACACAGACTATAATGAAGAGAGACTATAATGTGATCTGTCCACAAGAAATATATGGTTATTTACTGCTCACACTGGCAGCGAGTTTATGTGCTTCTCTCTCCTGTTTTCAAAGGCACTTTTACAAGCCGCTGCTGAGA[C/T]GAGGTGCCGGCAAGTTACTGAGCCAATCAGCTGTGTTTTTCGCCTCTGCTTTTTTTCATGAGGTGAGATGTGCATAAATCACACGTTGTTTTAAATATTCTGTCAGGTCATGGCAAATGAAAGTTAACAGTCTGAGCCGGGTAACAACCTGTGTGAATTATTTCTCATTTTAGAAATGTGCTATTTCTCATAAGCAGTAGCAATACATATTTTAGAGTGTTTACTATTAATATCTTTAAAAAAGTCTAAACATAAAATATGTATAACCTAAACCTTCATGTACCGCTGACTCAAAGTAATCTTTAAAAGCACTATTTATTGAATGTGCGCTTTAACAAAACTAAAAATTTATGTTGTTTTTTTTTTCTTTTAGCGTTAAAATGATTTGATTTGTTTGTGGTTTAAGAAATTTCTTTGACGAAATGTCAGTATATTTAAACAATTTGTCTTTTATTAAATATGTAATCATTTAAATGTATGTCCTATTAAATGGACTATAA
Associated Phenotype:
Normal
| Stage | Entity | Quality | Tag |
|---|---|---|---|
| Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa39109
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000077185 | Nonsense | 432 | 507 | 15 | 17 |
| ENSDART00000147890 | None | None | 78 | None | 3 |
Genomic Location (Zv9):
Chromosome 16 (position 33282086)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 31020601 |
| GRCz11 | 16 | 30978528 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAAGTTACTGAGCCAATCAGCTGTGTTTTTCGCCTCTGCTTTTTTTCAT[G/T]AGGTGAGATGTGCATAAATCACACGTTGTTTTAAATATTCTGTCAGGTCA
Long Flanking Sequence:
CAAGCTAATTTGTTTAGCTGTCTATTCAAAGCATAGGACGGTTGTGACCTCTATTTTACAGTTATTGTTTTTGCATTATTATTAAATGAGCAGCTAGAGGTACCACTTCCCCAACATGCTGCATTTGAAAGGCATAAGTCTCAGATGTATTGTGACCCTGTGTTTGTTTCAGGAACTCTGAAACGATAACGTACTTCTGGCAAAACTGGAATATTCCCGTGCACAAGTGGTGCCTCCGGTGAGTGAACGGCAGGTTTGAAAGCGACAACAGACAGCTGTTGAAATACGACACAGTAAAACCCACACAGACTATAATGAAGAGAGACTATAATGTGATCTGTCCACAAGAAATATATGGTTATTTACTGCTCACACTGGCAGCGAGTTTATGTGCTTCTCTCTCCTGTTTTCAAAGGCACTTTTACAAGCCGCTGCTGAGACGAGGTGCCGGCAAGTTACTGAGCCAATCAGCTGTGTTTTTCGCCTCTGCTTTTTTTCAT[G/T]AGGTGAGATGTGCATAAATCACACGTTGTTTTAAATATTCTGTCAGGTCATGGCAAATGAAAGTTAACAGTCTGAGCCGGGTAACAACCTGTGTGAATTATTTCTCATTTTAGAAATGTGCTATTTCTCATAAGCAGTAGCAATACATATTTTAGAGTGTTTACTATTAATATCTTTAAAAAAGTCTAAACATAAAATATGTATAACCTAAACCTTCATGTACCGCTGACTCAAAGTAATCTTTAAAAGCACTATTTATTGAATGTGCGCTTTAACAAAACTAAAAATTTATGTTGTTTTTTTTTTCTTTTAGCGTTAAAATGATTTGATTTGTTTGTGGTTTAAGAAATTTCTTTGACGAAATGTCAGTATATTTAAACAATTTGTCTTTTATTAAATATGTAATCATTTAAATGTATGTCCTATTAAATGGACTATAAAATGTAATTAATTATTGGCTTATTAGTATTAATCAAAATTGTAATAGTTTAAAGGGTACT
Associated Phenotype:
Not determined