ZMP
zgc:112165
Ensembl ID:
ZFIN ID:
Description:
Lysophosphatidylcholine acyltransferase 2 [Source:UniProtKB/Swiss-Prot;Acc:Q502J0]
Human Orthologue:
LPCAT2
Human Description:
lysophosphatidylcholine acyltransferase 2 [Source:HGNC Symbol;Acc:26032]
Mouse Orthologues:
Lpcat2, Lpcat2b
Mouse Descriptions:
lysophosphatidylcholine acyltransferase 2 Gene [Source:MGI Symbol;Acc:MGI:3606214]
lysophosphatidylcholine acyltransferase 2B Gene [Source:MGI Symbol;Acc:MGI:1918152]
lysophosphatidylcholine acyltransferase 2B Gene [Source:MGI Symbol;Acc:MGI:1918152]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa6082 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa31581 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa6082
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 |
---|---|---|---|---|---|
ENSDART00000074963 | Nonsense | 333 | 529 | 10 | 14 |
ENSDART00000128334 | Nonsense | 333 | 529 | 10 | 15 |
Genomic Location (Zv9):
Chromosome 7 (position 36854007)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 35127850 |
GRCz11 | 7 | 35399327 |
KASP Assay ID:
554-3784.1 (used for ordering genotyping assays)
KASP Sequence:
AACTGACTCTGCCTATGGAAGCTGGACTAGTGGAGTTTACCAAGAYCAGC[A/T]GAAAATTGGAGTAAGAAAAYAGTTTATACGTGTAATTTTAAGAATACCAA
Long Flanking Sequence:
TATTTACGCAATAAGTACATTGTAATGAATGATTAATTTCAGTGTAAGTACATTTTAATTAAGGACACTTAATATAAAGTGGGGCCGACTTTTTTTTCAAATCAAAGTTAAAATTACCCAGTCAAAGTGCACTTTTGCTTATGCTTTTGAAAACACTATTGGTTGGGTTTAGGTCAGTGGTTCTATAGGCGATCTATATGACAAGTCTTGCCTTCTTGTGAGCAGATGACTAGAATAATGCTTAATGCACTATAAAATGTAGCATAAAGCATACATTTTCATTGGGCCTCGATTGGAGATTATATTTCACAGACATTTAAATTGTAAACACAGTAAAGTATTTCAGTGTAAATATGTTTATCACAAGTTATTGTGCGTTTACTAGATCTCTGAAGCTGCCAGTCACAGACCACACTTATGAAGACTGCCGTTTGATGATTGCTGCTGGAGAACTGACTCTGCCTATGGAAGCTGGACTAGTGGAGTTTACCAAGATCAGC[A/T]GAAAATTGGAGTAAGAAAACAGTTTATACGTGTAATTTTAAGAATACCAAATATGCATAAACTTGTTGTTTTCATATTGGTGGTGTAATGGTACACCTAAATTAGGGTTAAATATGTATCTTGGTCTTAAAATCACAATGTGATACATTTTCAGTAGAACCTGAAGAAACCAAAACCTGAAAATGTCTTCTTTTTTAATGAAACACTTATTTACTGAACAATTTGTGGCTTTATTTTTAAAGAAATATAATTAGCATTTCAATTCGTCGAATACAAATTTGGAAAAGAATAAACACAAATGAACACATAAGCTAATATAATAATTTAAGCAAGCTGTGAGCACTTAAAGAGGTAAATGTAATGCTACTTGATATATTGGTTATTTATAACGAACTGTAAAGAGGAAGGAAGGAAGAAAAGGAAGGAAGTACTGTCTTCATTTGCGCTTTGTAACTTTTATTAAAGCCACCTATACAACAATCTGTCTCTGTTACAACCGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31581
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
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000074963 | None | None | 529 | 14 | 14 |
ENSDART00000128334 | Essential Splice Site | None | 529 | 14 | 15 |
Genomic Location (Zv9):
Chromosome 7 (position 36848357)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 35122200 |
GRCz11 | 7 | 35393677 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGAAAGATGACTGACTCAGATGAAGGAGATTGAGCATGCAGACATAAGG[G/A]TAATACTCCAAGCCATGCCATCTGAACATGTGCCTTAAGCCTGCATGGGT
Long Flanking Sequence:
TCAAATTGTTTTGAAATGAGGAATTAGTTTTGTACTGTAGTACTTTCAGGAAGTTTTAATGACCTCTGAGCTCATTTCAGGTCATCAGCTACATGTTTTAGCCTACTTGAATACCTCAAATACATTTTCAGGAAACATCTGTGCCTGATTCAAACATACTCTTTACCTATTATAGCTGGTTACTAATTTCATCCCTGTCTATTACCTCGCTTCATTAGTCTGCTTTCATTTTGAGTTCAAATTTCTACTAACTTTGCTATTTCAATGTCTCTGTCAGATGAGTTTCGTTCCTTCGCTCTCAATCATCCCGAATATGCAAAGCTCTTCACCACCTACATCGAGCTCCAGCGTTACCAGGGTCTACAGGGGGACGAGACTGACTTCGACAGTGCTTTTTCTCACTGCTGTACTGCTGCTTATGATGAGTATCAGGAGGACAGTGCCTCTGATAAGAAAGATGACTGACTCAGATGAAGGAGATTGAGCATGCAGACATAAGG[G/A]TAATACTCCAAGCCATGCCATCTGAACATGTGCCTTAAGCCTGCATGGGTGGTGTGCTTCTGCAGACGAGCACATGCCCTATCAAAAAATCTAGTTTTCTGTTTACAGCATCAAGTGTTTCATAAACTATTTAATGATTTATTTAAAAGCTTGTTTATATGTATAAGCATGCTGAAACTGTTCTTATTGTGATTAAGGTAAAAACATATCTGCAGCTTTTAGACTTAATGGCATGTAATTCCACAGTTTTATATGAAATCTAATTAATACTTTTGAATTGCTTATAAATAATTAGAGGAAATGTAGATTTTTTTAGATTAGGTACTTTCATTACACACACATGAAAAAACATGAAAGTTTTTTTTTAACTTGTATATTATTGCATTCATTCATTTTCTTTTTAGCTTAGTCCCTTTATTATTCAGGGGTGGCCACAGTGGAAAACAACACCAACTTATTTATGTTTTTGCGCAGCCCTTTCAGCTACAACCCATCACTGG
Associated Phenotype:
Not determined