ZMP
agpat3
Ensembl ID:
ZFIN ID:
Description:
1-acyl-sn-glycerol-3-phosphate acyltransferase gamma [Source:RefSeq peptide;Acc:NP_998590]
Human Orthologue:
AGPAT3
Human Description:
1-acylglycerol-3-phosphate O-acyltransferase 3 [Source:HGNC Symbol;Acc:326]
Mouse Orthologue:
Agpat3
Mouse Description:
1-acylglycerol-3-phosphate O-acyltransferase 3 Gene [Source:MGI Symbol;Acc:MGI:1336186]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa9087 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa19560 | Nonsense | Available for shipment | Available now |
sa39676 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa32749 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa9087
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000115081 | Nonsense | 68 | 377 | 4 | 10 |
ENSDART00000135795 | Nonsense | 68 | 116 | 4 | 4 |
ENSDART00000145167 | Nonsense | 68 | 221 | 4 | 6 |
Genomic Location (Zv9):
Chromosome 1 (position 47351328)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 46162989 |
GRCz11 | 1 | 46854221 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTWCTCTCTTTTATCTTTATATTAGAGTTAGTGATGTTGTTGGAGTGGTG[G/A]TCTGGCACTGAGTGCACGCTGTAYACCGATCAGGCMACGGTGGATAAATT
Long Flanking Sequence:
CATGCACAGGACAAGAGCGCCAGTGCACTCATCACACACCAGCTGTAGGTGAAATTGAGAGATCGTAGTAGAGCCAATTTGGTGGATGGGGATGATTTGGAGGCCATGATGGGAAAGGGCCGATGGAGGCAATTTGGCCAGGACAACGGGGTTACACCCCTACTTTTTACGATAAATGCCATGGTTTTTAAATAACCACAGAGAGTCAGTATCTCGGTTTAACGTCTCATCCGAATGACCGTTTAGCAGTACAATCAAAATTAAATATCCAAGAGAATTATTTTCTAATGCATCCTTTTGACCATCTAATTCACCACCTAATTCAAATGTATTTGAATATTTGGGTTTATTAATTTAGCAATTTATCCAATGGAGGCAACATTTGTCATGGCTCTTGTCATAATATTACTATTATAAAACCTTCTTGACGTGCATTATTTCTGTGTGTGTTTTCTCTCTTTTATCTTTATATTAGAGTTAGTGATGTTGTTGGAGTGGTG[G/A]TCTGGCACTGAGTGCACGCTGTACACCGATCAGGCCACGGTGGATAAATTTGGTAAAGAGCATGTCATCATCATCCTCAACCACAACTTCGAGGTGGACTTTCTGTGTGGCTGGACCATCTGTGAGAGATACGGCGTGCTGGGGGTGAGTCCCGATGAGCAGTGAAGAGATGAAACTGAGTGAGAAGTTGTGAAGGACGGTGTGAAAGTTGTGTAGGCCTGTGTCTCAAAATAAAAAATAATAACAAAATAAAATAATAATCCATCGATCAACTACATTTATTACATAACATTTATCTATAGATACTACCTATTTCATTTGCTTACATGGTGTTTATTCCTTGGGTACTACTATCTTTTTAAATGATACTTTTACTAAAAGTTATACTTTTAAAAACATTTATTAGAAACTACACTCAAAGAAACAATTTTTGCTGCTTGTTCAAATGACTTATTTGAAATGAGTTGAGTTCTTGAATTCTGTTGGGAGAACCTAATTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19560
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000115081 | Nonsense | 109 | 377 | 4 | 10 |
ENSDART00000135795 | Nonsense | 109 | 116 | 4 | 4 |
ENSDART00000145167 | Nonsense | 109 | 221 | 4 | 6 |
Genomic Location (Zv9):
Chromosome 1 (position 47351205)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 46162866 |
GRCz11 | 1 | 46854098 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCCTCAACCACAACTTCGAGGTGGACTTTCTGTGTGGCTGGACCATCTG[T/A]GAGAGATACGGCGTGCTGGGGGTGAGTCCCGATGAGCAGTGAAGAGATGA
Long Flanking Sequence:
TGGAGGCAATTTGGCCAGGACAACGGGGTTACACCCCTACTTTTTACGATAAATGCCATGGTTTTTAAATAACCACAGAGAGTCAGTATCTCGGTTTAACGTCTCATCCGAATGACCGTTTAGCAGTACAATCAAAATTAAATATCCAAGAGAATTATTTTCTAATGCATCCTTTTGACCATCTAATTCACCACCTAATTCAAATGTATTTGAATATTTGGGTTTATTAATTTAGCAATTTATCCAATGGAGGCAACATTTGTCATGGCTCTTGTCATAATATTACTATTATAAAACCTTCTTGACGTGCATTATTTCTGTGTGTGTTTTCTCTCTTTTATCTTTATATTAGAGTTAGTGATGTTGTTGGAGTGGTGGTCTGGCACTGAGTGCACGCTGTACACCGATCAGGCCACGGTGGATAAATTTGGTAAAGAGCATGTCATCATCATCCTCAACCACAACTTCGAGGTGGACTTTCTGTGTGGCTGGACCATCTG[T/A]GAGAGATACGGCGTGCTGGGGGTGAGTCCCGATGAGCAGTGAAGAGATGAAACTGAGTGAGAAGTTGTGAAGGACGGTGTGAAAGTTGTGTAGGCCTGTGTCTCAAAATAAAAAATAATAACAAAATAAAATAATAATCCATCGATCAACTACATTTATTACATAACATTTATCTATAGATACTACCTATTTCATTTGCTTACATGGTGTTTATTCCTTGGGTACTACTATCTTTTTAAATGATACTTTTACTAAAAGTTATACTTTTAAAAACATTTATTAGAAACTACACTCAAAGAAACAATTTTTGCTGCTTGTTCAAATGACTTATTTGAAATGAGTTGAGTTCTTGAATTCTGTTGGGAGAACCTAATTGTTTTATGTTCAGTCCACTTAAACTTGTTAAAACAATTACGTTAACGTAATCGATTTGTGTTGGTACAACATGAAGGAACAGTGCCTATTAAACAGATGCAAGTGACCATTCATTATATTCTAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39676
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000115081 | Essential Splice Site | 222 | 377 | None | 10 |
ENSDART00000135795 | None | None | 116 | None | 4 |
ENSDART00000145167 | None | 222 | 221 | None | 6 |
Genomic Location (Zv9):
Chromosome 1 (position 47345649)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 46157310 |
GRCz11 | 1 | 46848542 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCCGCACCAAAGGATTCACCACCACACTGCAATGCCTAAAGGGAACAGG[T/G]CAGACAAACACTTGTGCACACACCCCGTCATTGTCACACACAGTTTACAC
Long Flanking Sequence:
ACTCCACCTGCGAGGTCACTTATACCATGGTCCGATTGGAAGTTTCCGTTGGCAACAAGAGCCAGAGATTACAAAGTGATAGGATTACTCTGTTTAACACTGACCTGAGAGTTACAATCCTCTCGTGTGTGTGTGTGTTTGTGTGTGTGTTTGTGTGTGTGTTTGTGTGTGTGTGTGTTTGTGTGTGTGTTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTGTGTTTGTGTGTTTGTGTGTTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTGGCAGTTCCTGTTGTACTGTGAAGGAACGAGATTTACGGAAAAGAAACACCAGATCAGCATGCAGGTGGCTGAGAGTAAGGGCCTTCCCAAACTGAAGTACCACCTCCTGCCCCGCACCAAAGGATTCACCACCACACTGCAATGCCTAAAGGGAACAGG[T/G]CAGACAAACACTTGTGCACACACCCCGTCATTGTCACACACAGTTTACACCAAGACATTTTGATTTGGTGTAGTGTTTGTTTCAGATAGTATACCGATCATTTACTCACACACAAGTGCTTCTCTTTTATGACATAAAACAAGATATTCTGAAAAATGTTGGGGAAAAAAGCAATTGGCATTTATAGTATAAACAAAAAAAATACTATGGAGGTCAATGGCAACATACACTCACCAGCCACTTTATTAGGTACACCTTGCTAGTATCGGGTTGAACTCCCTTTTGCCCTCAAAACCGACTTAATCCAAAAAGATTTTGGTCTAAATTGACACAATAGCAGTTGCTGCAGATTTGTCAGCTGCACATTCATGATACAAATCTCCCATTCCACAACATCCCAAAGGTGCTTTATTGGAATGAGATCTGGTGACTGTGGAGGCCATTTGAGTACAGATGATTCACACTTTACCACATGGCACTTTATCCTGCTGGAAGTAGCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32749
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 |
---|---|---|---|---|---|
ENSDART00000115081 | Nonsense | 253 | 377 | 7 | 10 |
ENSDART00000135795 | None | None | 116 | None | 4 |
ENSDART00000145167 | None | None | 221 | None | 6 |
Genomic Location (Zv9):
Chromosome 1 (position 47340303)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 46151964 |
GRCz11 | 1 | 46843196 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAACCCGACTCTGTTGGGGATTGTCAATGGGAAGAAGTACAAAGCAGACT[T/A]GAGTGTCAGGTGAGTCTCCCAGTTCACTGATATCACTGTATATAATAAAT
Long Flanking Sequence:
AAGCATAATCTAGAGACCTTTGCCTTTCATATAAGCCACTTCTGATACCAAATGGTCAACTAGAAGTTATTAATTGTTCCTTAAACCTAAATGGGTAACAAGACTTTAGTCAAGTAGTGTATATAGTAGAAACTACTATATATACTACACTATTTATTACAGTATATCAGTTTAGTGTTAATACTACACTGCTGTAGAATTTATCAACACTAACAACATTAACAGTGACATTTATTAACAGTAATATATACAGTATAATACACTTTGATATAGCATGGTTTAAAAGCACTAGCATTTACTATAATTTCATATTATATATATTTATTCATATGGGAATTATTCTTTTAAATAAACTAATTCCGTTATATCACATTCTAAAGATAGAATTGTCTGTTCTATTTCAACAGTAAAAGCAGTCTATGATGTCACGCTGAACTTCAAAGACAAACAAAACCCGACTCTGTTGGGGATTGTCAATGGGAAGAAGTACAAAGCAGACT[T/A]GAGTGTCAGGTGAGTCTCCCAGTTCACTGATATCACTGTATATAATAAATTACAATATCATTTGAAAATAAATAGATCATCATACACATTTTAGACTGTCCAGTTAACATTAAACTGTCACATTTTAGGAATGTTGTGCATCTTACTGCTGACCTGAGATTTTCCTGAAATATTTGGATTAAGGTTGTGACTAATAGGATTTGTACCTGGTTAAGCTTTCCCCCTGCTGTTCTGCATGCAGTTATGGCGCCCTCTATTGGAGTGTATTGTGCTGCACTTATGAAGCGTCACTGTTCTGTTTACAGGCGCTTCTCTGTTGAGGAGATTCCTGACGATGAAAAAGAGTGCGCCGATTGGTTACACAAACTCTACCAAGAGAAGGTTTGAAGCTTTTACTGAGTCTTGATTAAATTTTTTAGTTATGACATAAAATGGTGTAATGTTTTTGTGAAGGAAAATACATACTTGTAGTGTGAACAGAAGAGTTGTCGATCCTTGGG
Associated Phenotype:
Not determined