ZMP
mogat2
Ensembl ID:
ZFIN ID:
Description:
2-acylglycerol O-acyltransferase 2 [Source:RefSeq peptide;Acc:NP_001006083]
Human Orthologue:
MOGAT2
Human Description:
monoacylglycerol O-acyltransferase 2 [Source:HGNC Symbol;Acc:23248]
Mouse Orthologue:
Mogat2
Mouse Description:
monoacylglycerol O-acyltransferase 2 Gene [Source:MGI Symbol;Acc:MGI:2663253]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa41689 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa41688 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa41689
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 |
|---|---|---|---|---|---|
| ENSDART00000017436 | Essential Splice Site | 135 | 252 | 4 | 6 |
| ENSDART00000128888 | Essential Splice Site | 251 | 368 | 4 | 6 |
| ENSDART00000143301 | Essential Splice Site | 213 | 330 | 4 | 6 |
The following transcripts of ENSDARG00000019228 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 10 (position 33496292)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 32597641 |
| GRCz11 | 10 | 32541501 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTCACCTGGCCAATAAGAAAGGCTTTATTAAGCTTGCAATAGAGCACGG[G/A]TAAGCAAGAGCTTTCTCCTGATCACTTAATAGTTTAACAGGTTGTCTCTT
Long Flanking Sequence:
ATGAACCACCAACTTATCCAGCAGGTTTTTACGAAGCGGATGCCCTTCCAGCTGCAACCCATCTCTGGGAAAAGAGCAGTTCAATCTCTTATGAAGTTTGCTGTATAAAAATATAACATTTTGAATTATTTATAATTATCGGCCTATACATATCAGCTATACGGCCTCCAAGTCTAAAGAGTTATCGGTTATCGGCCAAAAAAATCCATGTCGATTCATCCCTAGGTAAAGGCATTAGAAAATACAGTTTTACCAGCATAAAATCAATGGAAACCTATGTAACATCCCTACTGCTCACAAAAACAAACACGTGTGTGTATTCCAGGGCTGGTTCCATCAGACAAGGAGAGTGCCGGTTATCTGCTCCGGAGGAAGGGCGGAGGGAATGCGGTGGTCATTGCAGTCGGTGGAGCTCCTGAAGCTTTGGATGCACATCCTGGTGACTACACCGTTCACCTGGCCAATAAGAAAGGCTTTATTAAGCTTGCAATAGAGCACGG[G/A]TAAGCAAGAGCTTTCTCCTGATCACTTAATAGTTTAACAGGTTGTCTCTTGTTGACACAAGATTTTGTCTTTTGTGTTTGTGCCAATTATTTGTTGCCAGATTGCCAAAGTTGCTCATTTATGAAATGCAAACTTGTGCAACTTGCATTGGAACGTAATAGTTCTACATTTACATAACGCTCTGTGGCAAAAACTAAAGAGTTTGAAGGGTTAGTTCACCCAGAAATGAACATTTATCATTCATTCTCATGTCATTCCAAACCCCTAAAACCATCATTCACTTTCAAAACACAAATGTGACCCTGGATTTGAATTGGGTTTATTTTTGGCAGTAACCAAAAATACATTATTGTATGGGTCAAATATAATTTTTTATTTTATGGCAAAAATCATTTGAATTTAACGTTAAGATCAAGTTGTATAAATACATTTAGCAAATTCCCTACAGTAATTTTTACAAAAGTCAAATTTGCATTAGTTAATGTGCATTGCTGGGGGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41688
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 |
|---|---|---|---|---|---|
| ENSDART00000017436 | Essential Splice Site | 135 | 252 | 5 | 6 |
| ENSDART00000128888 | Essential Splice Site | 251 | 368 | 5 | 6 |
| ENSDART00000143301 | Essential Splice Site | 213 | 330 | 5 | 6 |
The following transcripts of ENSDARG00000019228 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 10 (position 33494017)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 32595366 |
| GRCz11 | 10 | 32539226 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTCTCGCTTCTGTTTTTAATCAAAACTATCTTATTTTATTCTTACTGTA[G/A]TGCAGATTTGGTTCCTATATATTCGTTTGGAGAGAACGAGGTGTTTGACC
Long Flanking Sequence:
AAAAAAATGTGTGTGACAAAATTCTGTAAACAAGACTGTGTTTGCTAAAGAGATTAACAGTTTTTCTTTATTTTGCCATGAAAAAGTGTTCTTGGAGTTTAGTATCATTCAGAAATCACATTGTTTTAATGAAGGGTTTGGTTCCTTTTCTGGACTTTGAACATATCTAGAACTTTACCGTCTATGGAGGGTCATCTAAAATAAGCATTTTGTTTAAATTATATTGATTTGAGTAATTAAGAACAGAACTTTCAATTTTGGGTTAACTAATCATTTAGCAATCTGTACATTCTACCAATGACATAATTTCAATGTCAAGATTCACATCTGCATTAGATTTTTGTCTGCAAATTTGATTCTGACATTCTACTTTCAGATAGTTTATATGTTAAATCTGCACATGAATGTTTCATGTCTCTTTATTTATTTCATTTGTAGACATTATTTTCCTCTCTCGCTTCTGTTTTTAATCAAAACTATCTTATTTTATTCTTACTGTA[G/A]TGCAGATTTGGTTCCTATATATTCGTTTGGAGAGAACGAGGTGTTTGACCAGGTGCAGAATCCTCGTGGCACATGGCTGCGATACATTCAAGAGCGTCTGCAGCGCATCATGGGTGTTTCTCTTCCTCTCTTTCATGCGCGAGGAGTTTTCCAGTACACCTTCGGCCTGATGCCTTACAGAAAGCCCATCAACACTGTTGGTGAGTACAAGCAAATATTACTGAAACTTTATTAAGACTAATTTCAAACGACCCTTTGTCATGCTATACAGATGAAATGACCTCTCTCAGTTTTCTGAGTCATGTATTTTTTGTAGTGTAGAAATGCTTAATCTTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTAGTCTGTCTGTCTGTCTGTCTCTGTCTCTGTCTCTGTCTCTGTCTG
Associated Phenotype:
Not determined