ZMP
lpcat4
Ensembl ID:
ZFIN ID:
Description:
lysophospholipid acyltransferase LPCAT4 [Source:RefSeq peptide;Acc:NP_991122]
Human Orthologue:
LPCAT4
Human Description:
lysophosphatidylcholine acyltransferase 4 [Source:HGNC Symbol;Acc:30059]
Mouse Orthologue:
Lpcat4
Mouse Description:
lysophosphatidylcholine acyltransferase 4 Gene [Source:MGI Symbol;Acc:MGI:2138993]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa38589 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa40820 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa38589
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 |
|---|---|---|---|---|---|
| ENSDART00000050687 | Nonsense | 182 | 508 | 3 | 13 |
Genomic Location (Zv9):
Chromosome 7 (position 1664135)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 1347454 |
| GRCz11 | 7 | 1483534 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAGAAGTGCGTGTCTCAGATCTGTGAGAGAGTGACGTCTGATGGACACT[G/A]GCCTCAGGTATGAACGCGCGCATACACACACACCAACCTACTCAATCACA
Long Flanking Sequence:
TGAAGGAGTATTCAGAATGTAGCCTGAACAAAACCTGATTGTATTCTAGTTCTATTCAAGCTTTGTTCAAGCTATGTTCTGGCTATAATTAAGTAATGTTCTGGTTGGGTTCAAACTATGTTCAAGATCCGTTTTGGATCTATTCTAATTGTTATTATTCTAGATTATGTATATAGTTTTAATCCATTTTTAACTATTAAGTTATTTTTAATTTAGTAGTTTTTTGTTGTATTTTTCAGTTAAATGTGACTGTTAAAAATGGAAATACACAGTATGCGCTTAACACAAGCTTATCTTTATATTCTTGTCATTATAAATGTTAATGCTGTACACACACACACACACACGCACGCACACACACGCGCACACACTGAAGTGTCATCTGTGTGTTCCAGCTCTGTTGGAGTTTAATCAGTCTGTGCTTGTCAGTCGAAAAGATCCGGAATCCAGGAAGAAGTGCGTGTCTCAGATCTGTGAGAGAGTGACGTCTGATGGACACT[G/A]GCCTCAGGTATGAACGCGCGCATACACACACACCAACCTACTCAATCACACACACCTGCACTCACAAACTCCACACAAACACAAATGCTATCTATCTCTAACACACACACACACACACACACACTAACCCAGGTGTGTCCAAGCTTGGTCATGAAGGGCCGCTGTCCTGCATATTTTAGTTCCAACCTCTATTAAACCCACCTGAACCAGCTAATCAAGCTCTTTCTAGCTGTACTAAAACCTAGAAAATACTAGAATTTACCCAGAACCTAGAAAGTAAATGAAATACTTCCTGGCCGGTGTGTTGAAGCAAGTTTGAGCTAAATATGCAGGACACCGGCCCACCAGGAGTGAGTTTGGACACCCCTGCTCTAACCTATTCACTCACACTCTTCAAACACACACACGCACTATCTCTTTCTCTCTCTCTCTCTCAAACACACACACATTAACACTTATTCTCCTTCTCATTTACTCTCAGACATGCACACACATGCTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40820
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 |
|---|---|---|---|---|---|
| ENSDART00000050687 | Nonsense | 182 | 508 | 3 | 13 |
Genomic Location (Zv9):
Chromosome 7 (position 1664136)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 1347455 |
| GRCz11 | 7 | 1483535 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGAAGTGCGTGTCTCAGATCTGTGAGAGAGTGACGTCTGATGGACACTG[G/A]CCTCAGGTATGAACGCGCGCATACACACACACCAACCTACTCAATCACAC
Long Flanking Sequence:
GAAGGAGTATTCAGAATGTAGCCTGAACAAAACCTGATTGTATTCTAGTTCTATTCAAGCTTTGTTCAAGCTATGTTCTGGCTATAATTAAGTAATGTTCTGGTTGGGTTCAAACTATGTTCAAGATCCGTTTTGGATCTATTCTAATTGTTATTATTCTAGATTATGTATATAGTTTTAATCCATTTTTAACTATTAAGTTATTTTTAATTTAGTAGTTTTTTGTTGTATTTTTCAGTTAAATGTGACTGTTAAAAATGGAAATACACAGTATGCGCTTAACACAAGCTTATCTTTATATTCTTGTCATTATAAATGTTAATGCTGTACACACACACACACACACGCACGCACACACACGCGCACACACTGAAGTGTCATCTGTGTGTTCCAGCTCTGTTGGAGTTTAATCAGTCTGTGCTTGTCAGTCGAAAAGATCCGGAATCCAGGAAGAAGTGCGTGTCTCAGATCTGTGAGAGAGTGACGTCTGATGGACACTG[G/A]CCTCAGGTATGAACGCGCGCATACACACACACCAACCTACTCAATCACACACACCTGCACTCACAAACTCCACACAAACACAAATGCTATCTATCTCTAACACACACACACACACACACACACTAACCCAGGTGTGTCCAAGCTTGGTCATGAAGGGCCGCTGTCCTGCATATTTTAGTTCCAACCTCTATTAAACCCACCTGAACCAGCTAATCAAGCTCTTTCTAGCTGTACTAAAACCTAGAAAATACTAGAATTTACCCAGAACCTAGAAAGTAAATGAAATACTTCCTGGCCGGTGTGTTGAAGCAAGTTTGAGCTAAATATGCAGGACACCGGCCCACCAGGAGTGAGTTTGGACACCCCTGCTCTAACCTATTCACTCACACTCTTCAAACACACACACGCACTATCTCTTTCTCTCTCTCTCTCTCAAACACACACACATTAACACTTATTCTCCTTCTCATTTACTCTCAGACATGCACACACATGCTCAC
Associated Phenotype:
Not determined