ZMP
zgc:162485
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC558437 [Source:RefSeq peptide;Acc:NP_001082849]
Human Orthologue:
GPAT2
Human Description:
glycerol-3-phosphate acyltransferase 2, mitochondrial [Source:HGNC Symbol;Acc:27168]
Mouse Orthologue:
Gpat2
Mouse Description:
glycerol-3-phosphate acyltransferase 2, mitochondrial Gene [Source:MGI Symbol;Acc:MGI:2684962]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa38705 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa13863 | Essential Splice Site, Missense | Available for shipment | Available now |
| sa7153 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa41270 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa38705
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 |
|---|---|---|---|---|---|
| ENSDART00000075620 | Nonsense | 227 | 787 | 8 | 22 |
| ENSDART00000123288 | Nonsense | 29 | 378 | 1 | 8 |
| ENSDART00000129344 | Nonsense | 227 | 787 | 8 | 22 |
| ENSDART00000141349 | Nonsense | 29 | 589 | 1 | 15 |
Genomic Location (Zv9):
Chromosome 8 (position 43124272)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 41070259 |
| GRCz11 | 8 | 41104231 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGCAGCATCGATCACGCTCTTATTTGTCTCACTCTCTTCTGCCACAACT[T/A]GAGGGTTCCCTACACCATTTTTCCAGCCCACGTTCGACAAACCTGGTTAA
Long Flanking Sequence:
CTATCTATCTGTCTGTTTTTCAATTTGTCTATCACTGTATTTTTTAAAAATCTTATAGTAAGTATGTTGAACTAAAATTGCAGTGTAGACACTGTAATTTAAACATGCATGATTTATGCTTGTTTTTCTGGTGTTATGTTATGCGTCAAATACTTAATCAGAGTTAAGATGAACAGTGTTTTTAACAGGGCTGCTGTGACCTTTAATCTGTATTCTTGGTTCTCAGTGTTTATGTTAAATATATGTTAAATATTACTGCAGTTGGGTCCAGAAACACAATATAAGTGCCATTTTCCAAAGTACAAAAACAGTTCATTTACGGGTTCATTCTCAAGTACACACTGGTCAGCACTGAACTGTATTACTCACTGCGCTGAAGTGTCCTCTAAAGTTGTCCATCTATGTGTGTGTGTTGTAGAAAGCCCCTCTGGTCTATGTGTGTGTTCGGCAGAGCAGCATCGATCACGCTCTTATTTGTCTCACTCTCTTCTGCCACAACT[T/A]GAGGGTTCCCTACACCATTTTTCCAGCCCACGTTCGACAAACCTGGTTAAGGTAAATGCACACACTGATAATACAAAAACACTCACCCTGTAGCTCTCACAGATGCATTGTTTGCTTGGAAACCTTCTTTTCTCATTCCTCCACAGTTCACTACCCTACATGCCTTCATATTGTATTATATCGATCAAGTACACTGTGGAGTACCACAAGGCTCAGTTCTAGGTCTCTTGTTTCTTTGCATTTTATATCAGAGGTTGAACGTCTTCAGATTTTTATAAGTCGACTTTTTTGTTATTAACAGTCGCTGGTGACATCACCAATAAAACAAGGCACAAATATTTTTGCAACACGCCACAATTTGGTGTTTATTTCCAGAAAATGCATATACGCATGCTGTTTGACAGCTCATAACTAGGGTTGGGTTCCGAAACCCCTTTGTAACCGGTATGTACCGGACCGAATCAGCATAGGAAATTCAGTGCCTAATTTCGGTGCCACTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13863
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:
G > A
Consequence:
Essential Splice Site, Missense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000075620 | Essential Splice Site | 551 | 787 | 15 | 22 |
| ENSDART00000123288 | Missense | 354 | 378 | 8 | 8 |
| ENSDART00000129344 | Essential Splice Site | 551 | 787 | 15 | 22 |
| ENSDART00000141349 | Essential Splice Site | 353 | 589 | 8 | 15 |
Genomic Location (Zv9):
Chromosome 8 (position 43163253)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 41109240 |
| GRCz11 | 8 | 41143212 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAAGCAGTGCGATGTGATCACTCGTGTCTTCATACACGAGGCTGTAGGAG[G/A]TAGGCTTTGTGTGTTGGAGATCGAATGGAGGCAAGGAAACTTAATGTTGG
Long Flanking Sequence:
TATTACTAGCATCATAATCTAAATGCTTCTGAAAATGAACTCATATACTGCATTATTTTGTGCCGTTTAGGGACTCGCATTTGCTGATTAGGGCCATCTAGGATCTGAACACTCTTATAATAGTGCATTAACTGGTTTATTACTCATCTAGTAGCAGTAGATGATTCACACAAATGTCTAACATAATTCTGCACGCTTTAATGAGTCTGCTAATGATCGTCTCCCTCTTTCTCAGGGCGTGCGTGTGTCCATGCTGTGCCGGGACATCTGCTGGCTGTTGGAGGAGGTGTTGTTCAGAAACACAGACGTGGGTTTCGGTGGCTCTCTGGTTGGGCTGGTACATCACGCGGTGTCTCTGCTACGCCCGTATCTGCTTCTGGCTGCGGCTCCACCTACAGGAGAGCCCATCATTGCACCACGGTCCGATCCAGACTCTCTGCTCATACTGAGCAAGCAGTGCGATGTGATCACTCGTGTCTTCATACACGAGGCTGTAGGAG[G/A]TAGGCTTTGTGTGTTGGAGATCGAATGGAGGCAAGGAAACTTAATGTTGGCAGGTGTCATGCACATATCTTTTTAGTGGGAGTCCTGGCTTATTTAGTGGAACATGGCAAGATTAAACAAGATGACTCAAGAAAAAATTTGTCATTTGCTCTTAGTCGTGTTGGCTTATTGGATTGCGTTAGGCCTGTCATGATCATTTTCAACATTTGTTTTGTGATGCAATAATGACCATTGTGTTCGCATAAAAACGAACGTCAAAAAATCTGGTTAAAAAGAAGCAGTGGGTGGAATTGGTGGACAAAGTACACGAATCAAGCACAGGAGTGAAAGAACAGATTATTAATAAAAACATAATTATTAATTTTTTTACTTGTTCTGGTTGACATATTACCGTTTTTCTCCATTGGTTTGGATCATTTCTTGAAACAGGAATTACATTCTCAAAACAACATGGACAAAACTCCAAACCACTTGGCAAATTTTCACAGAAGAGATTTTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7153
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000075620 | Essential Splice Site | 625 | 787 | 17 | 22 |
| ENSDART00000123288 | None | None | 378 | None | 8 |
| ENSDART00000129344 | Essential Splice Site | 625 | 787 | 17 | 22 |
| ENSDART00000141349 | Essential Splice Site | 427 | 589 | 10 | 15 |
Genomic Location (Zv9):
Chromosome 8 (position 43172872)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 41118859 |
| GRCz11 | 8 | 41152831 |
KASP Assay ID:
554-4725.1 (used for ordering genotyping assays)
KASP Sequence:
TGATGTTGTGGACAGCATGGTGCGCTGTGGGGTTCTGGTTATGGAGGAGG[T/C]AAAGACACCTGCTTTAACAAACACATACATTCATCCTCTGATCACAGTTA
Long Flanking Sequence:
CATCTCACTATGACGTTTCTAATCACATTTGCGCTAGTAGTGATTCATCCAGCCTTCTTGCTCTTCAGCCAGTCAGTAAAAAACAAAAACAAAACTCATTAATTTTTTTCATACATTCTCCAAATGTTTCTCTCACACGTCCAATCGATCAGTCGCTCCCCCATCTGTTCCCTTTATTATTCCCTCTTGATGTCTCTTAAATCGAGTTTCCTGTTCGAGGGTTCTTCAGCGGCAGGAATAGCGCGTGTAATTATTGCCAGCGCATTTTACACTTGCATCAGCAAATAAACACTTGTGAAGGCTGCGAAATGTCAACAAGAACAAAACCACTACACAACTAATTATCTCTCTGTCTTTCTCTCTTTCATGTCTGTCCGTCTGTGTGTGTTTGTCTCTCTCTCTCTCTCTCTCTCTCTCTCAGCCGTGTCAGAATGCTCATAGCTTTGCTCTTGATGTTGTGGACAGCATGGTGCGCTGTGGGGTTCTGGTTATGGAGGAGG[T/C]AAAGACACCTGCTTTAACAAACACATACATTCATCCTCTGATCACAGTTAAGCTTTGTACATTGTACACTTTAAAATCCTCTTCATAGCTTAGTCTAAATTAACTTTTCAGCGGCTGTCTGTTGGGTTCTAGTGAGTAGAGCAAGTAAATATTATGTAACACAGATTTACAACTTATTTAAGAGAGTTTATTACTAGTGCTGGGCAAAGATTAGATCATCACATCCAAAATAAAAGTTTGTTTTGACATAATATGTGTGTGTATCTTACATGTTTGTTATGTATATGTGACAAACACACATAAACATAATTGTGGGATAAATAATTCTGTTACATAAATATTTTAATTTCTACAGTTAGGTCCATAAATAGTTGAACATCGACCCAATTGTAACATTTTTGTCTCTAAACTCCAACACAATGGATTTGAAATTAAATGAAAAAGATGTGCTTTAGGTGCAGACTGACAGCTTTAATTTGAGTGTATTAACATCCAAATCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41270
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000075620 | Essential Splice Site | 667 | 787 | 18 | 22 |
| ENSDART00000123288 | None | None | 378 | None | 8 |
| ENSDART00000129344 | Essential Splice Site | 667 | 787 | 18 | 22 |
| ENSDART00000141349 | Essential Splice Site | 469 | 589 | 11 | 15 |
Genomic Location (Zv9):
Chromosome 8 (position 43176644)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 41122631 |
| GRCz11 | 8 | 41156603 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAGAGCAGCGATTCAGACTGTGAGGAACCAGACATACACACCTACAAGG[T/C]ATACACTTGTGCAAACATCTTTTAATATATCAAATTTACCATATATATAT
Long Flanking Sequence:
GACTTAAACTGTACGTTAACTGGCTTTCACAAATGTAGTGTTTTCAATAGAGTTTTTCAATGCCCAAAATTAAAGCTACAAACAGTGAATTTACAGAGACATGGCTAAAAATACAGTTTTCACTCTACTGCCCAAACATAGCAAGCTCTCAGACTCAATCTAATCTCTGACATGCTGACCATTCGGGGCTGTGTTTTTTTATTTTCGAGTGCTGCCACAGTTTTCAGCTGACTGACTCACAAACACATAAAAAGGTGCAAGCAAGTTTTTTTTGAGGGGATACAGATCACTTCAACCCTAAACTGATAATTTTGCAGCTTATTGGTATGTGTTTTTTAGAGACGTAAACTGTTGTGTGTGTGTGTGGGTGTAGGTCCAGACAGATGCACCGGTGTGTGACTTCATGAAGAGGCATGGTGTGTTATCATGGACTGTTTCAGACAATCCTGATGAGAGCAGCGATTCAGACTGTGAGGAACCAGACATACACACCTACAAGG[T/C]ATACACTTGTGCAAACATCTTTTAATATATCAAATTTACCATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTTGAGAATTCTTATCAAGGTGAAAAGTTGTCTTGTGAGTTGTGAAGTTATAATGGAATGTAAGGGTGAATTTAGCATCGAAGAATTGAGGCACGATTAGATTTGAACCGCAAGTCAAGTGCTTTGGCGTCGCTCGTATGCTTGAGTGATTGTGACCGCTTTTTTCATGGAGTTTAAAGATTGCTACAACTGCCACCACACCCATTAACCATATGATGGAATAGCACTTTATAAATGCTTAAAGTCAAAATCGCCATAAACATAAATCGAATTAAGACACATGTAGTATTCCTTCCTACATAGTCACAATATTGAAGTGCAGTACAGACATGTAAACACTGCAATCAAACTATTACCATCATGTAGGGCTTTTAGCC
Associated Phenotype:
Not determined